Flexible Work Environment

State-of-the-Art Offices

Workplace Journey

Training and Development

All the Perks

Health Insurance

Health Savings Account (HSA)

Vision Insurance

Disability Insurance

Mental Health Care

Supplemental Life Insurance

Dental Insurance

Large

People

Community

Compliance

Medpace is a UK-based clinical research organisation (CRO) that specializes in providing comprehensive and tailored services to pharmaceutical and biotechnology companies. Their ultimate mission is to accelerate the development of life-saving and life-improving therapies through high-quality and efficient clinical trials. Medpace's purpose is to collaborate with their clients to bring innovative medical treatments to market by offering expertise in study design, regulatory support, site management, and data analysis. They aim to advance medical knowledge and improve patient outcomes while upholding the highest ethical and scientific standards in clinical research within the UK and globally.

Science & Healthcare

Medpace

Pharmaceuticals

Accelerating Drug, Biologic and Medical Device Clinical Development

You need a Master's in Statistics/Biostatistics, good communication skills, SAS programming experience, and a readiness to apply innovative solutions and adapt to business needs.

You will analyze global studies, review analysis plans, collaborate with team members, generate specification documents, and efficiently produce QC derivations and outputs.

Data

Research & Development

Stirling

Our European activities are growing rapidly, and we are currently seeking a full-time, office-based Statistical Analyst to join our Global Statistics team. This position will work in a team to accomplish tasks and projects that are instrumental to the company’s success. At Medpace, Statistical Analysts go through an extensive onboarding and training process, which prepares them to become experts in their field. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you. Responsibilities * Support analysis for global studies; * Review analysis plans for appropriate methods; * Operate in collaboration with Project Statistician and other Statistical Analysts and Programmers to ensure study outputs are produced to a high quality and in a timely fashion; * Assist in generation of specification documents for derived datasets (e,g, ADaM) and tables, listings and figures; and * Use efficient programming techniques to produce and/or QC derived datasets (e.g. ADaM) and tables, listings and figures according to specifications. Qualifications * Master’s Degree in Statistics or Biostatistics, * Good communication skills; * Willingness to apply innovative programming techniques to solve critical problems; * Can adapt and respond to requests from across the business while being aware of impact of response; and * SAS programming experience and/or SAS Base Programming Certificate. Medpace Overview Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries. Why Medpace? People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future. Medpace Perks * Flexible work environment * Competitive compensation and benefits package * Competitive PTO packages * Structured career paths with opportunities for professional growth * Company-sponsored employee appreciation events * Employee health and wellness initiatives Awards * Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 * Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility What To Expect Next A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps. EO/AA Employer M/F/Disability/Vets

Our European activities are growing rapidly, and we are currently seeking a full-time, office-based Statistical Analyst to join our Global Statistics team. This position will work in a team to accomplish tasks and projects that are instrumental to the company’s success.At Medpace, Statistical Analysts go through an extensive onboarding and training process, which prepares them to become experts in their field. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you.Responsibilities * Support analysis for global studies; * Review analysis plans for appropriate methods; * Operate in collaboration with Project Statistician and other Statistical Analysts and Programmers to ensure study outputs are produced to a high quality and in a timely fashion; * Assist in generation of specification documents for derived datasets (e,g, ADaM) and tables, listings and figures; and * Use efficient programming techniques to produce and/or QC derived datasets (e.g. ADaM) and tables, listings and figures according to specifications.      Qualifications * Master’s Degree in Statistics or Biostatistics, * Good communication skills; * Willingness to apply innovative programming techniques to solve critical problems; * Can adapt and respond to requests from across the business while being aware of impact of response; and * SAS programming experience and/or SAS Base Programming Certificate.      Medpace OverviewMedpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.Why Medpace?People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.Medpace Perks * Flexible work environment * Competitive compensation and benefits package * Competitive PTO packages * Structured career paths with opportunities for professional growth * Company-sponsored employee appreciation events * Employee health and wellness initiatives      Awards * Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 * Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility      What To Expect NextA Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.EO/AA Employer M/F/Disability/Vets

Statistical Analyst (Stirling, Entry Level) - Medpace

Our European activities are growing rapidly, and we are currently seeking a full-time, office-based Statistical Analyst to join our Global Statistics team. This position will work in a team to accomplish tasks and projects that are instrumental to the company’s success.&lt;br&gt;&lt;br&gt;At Medpace, Statistical Analysts go through an extensive onboarding and training process, which prepares them to become experts in their field. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you.&lt;br&gt;&lt;br&gt;&lt;strong&gt;Responsibilities&lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;ul&gt;&lt;li&gt;Support analysis for global studies;&lt;/li&gt;&lt;li&gt;Review analysis plans for appropriate methods;&lt;/li&gt;&lt;li&gt;Operate in collaboration with Project Statistician and other Statistical Analysts and Programmers to ensure study outputs are produced to a high quality and in a timely fashion;&lt;/li&gt;&lt;li&gt;Assist in generation of specification documents for derived datasets (e,g, ADaM) and tables, listings and figures; and&lt;/li&gt;&lt;li&gt;Use efficient programming techniques to produce and/or QC derived datasets (e.g. ADaM) and tables, listings and figures according to specifications.&lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;&lt;strong&gt;Qualifications&lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;ul&gt;&lt;li&gt;Master’s Degree in Statistics or Biostatistics,&lt;/li&gt;&lt;li&gt;Good communication skills;&lt;/li&gt;&lt;li&gt;Willingness to apply innovative programming techniques to solve critical problems;&lt;/li&gt;&lt;li&gt;Can adapt and respond to requests from across the business while being aware of impact of response; and&lt;/li&gt;&lt;li&gt;SAS programming experience and/or SAS Base Programming Certificate.&lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;&lt;strong&gt;Medpace Overview&lt;br&gt;&lt;br&gt;&lt;/strong&gt;Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.&lt;br&gt;&lt;br&gt;&lt;strong&gt;Why Medpace?&lt;br&gt;&lt;br&gt;&lt;/strong&gt;People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.&lt;br&gt;&lt;br&gt;The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.&lt;br&gt;&lt;br&gt;&lt;strong&gt;Medpace Perks&lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;ul&gt;&lt;li&gt;Flexible work environment &lt;/li&gt;&lt;li&gt;Competitive compensation and benefits package&lt;/li&gt;&lt;li&gt;Competitive PTO packages&lt;/li&gt;&lt;li&gt;Structured career paths with opportunities for professional growth&lt;/li&gt;&lt;li&gt;Company-sponsored employee appreciation events &lt;/li&gt;&lt;li&gt;Employee health and wellness initiatives&lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;&lt;strong&gt;Awards&lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;ul&gt;&lt;li&gt;Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024&lt;/li&gt;&lt;li&gt;Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility&lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;&lt;strong&gt;What To Expect Next&lt;br&gt;&lt;br&gt;&lt;/strong&gt;A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.&lt;br&gt;&lt;br&gt;EO/AA Employer M/F/Disability/Vets

Statistical Analyst (Stirling, Entry Level)

You need a Master's/PhD in a relevant field, experience with LLMs/NLP, proficiency in Python and AI frameworks, strong communication skills, and a passion for AI advancements.

You will research AI tools, implement and fine-tune language models, integrate AI applications, contribute to architecture discussions, drive AI initiatives, improve processes, and mentor junior team members.

IT & Cybersecurity

London

Do you have a passion for Artificial Intelligence (AI) and looking to make a difference in how the latest clinical trials that can support new more personalised drugs progress into the market? Do you want to work in London with a great young vibe or do you prefer to work remote with a team of eager colleagues looking to make a difference in AI across the whole company? Medpace is open to those individuals passionate about AI wherever they are based in the UK. Do you have a background in data science and/or computer science with a run of working on AI projects and tools from Natural Language Processing (NLP) to Intelligent Automation (IA) to trying and training of Large Language Models (LLMs) for interactive AI applications across various IT systems? Have you worked with your IT colleagues to build out new AI applications that help users apply AI in their every day lives? Do you want to be using the latest AI tools and working on use cases that can be built into the latest deployed apps to make a difference in clinical trials? If so, we have an exciting opportunity for you to help take the reins of a groundbreaking project at Medpace. We are currently seeking a professional with direct experience interacting with artificial intelligence (AI) tools such as NLP, LLM, IA etc. Skills and training in natural language processing (NLP) and deep learning will be critical for this role. This professional will be expected to lead the programming and fine-tuning of various AI tools and helping the IT team to implement them into new applications. This professional will work collaboratively across the organisation with multiple teams to help design the roadmap for how AI can improve efficiency of company processes and provide insights and assistance to users. Applicants should have sufficient technical skills to help lead these types of AI projects independently and to train technical teams for support. Responsibilities * Research the latest AI tools from NLP to LLM to multi-agent capabilities to ensure we are maintaining a clear direction on the best in class AI; * Support the build and Implementation of private, large language models, fine-tuned based on both structured and text-based data inputs; * Integrate artificial intelligence to support AI applications that interact with the various AI tools through capabilities such as APIs; * Contribute to data and AI architecture review discussions, and support structural changes as needed; * Help drive AI technology thinking within the company across all departments; * Support departmental process improvement initiatives; and * Participate in educating, training and development of more junior team members. Qualifications * Masters or PhD in engineering, computer or data science, or related field. * Proven experience implementing and fine-tuning Large Language Models or interactive AI applications (either >1 year post-graduate experience, or PhD dissertation experience). * Strong background in Natural Language Processing (NLP) and deep learning. * Preferably several years of experience working with different AI capabilities and showcasing your passion both at work and outside work in the utilization of AI. * Technical proficiency in programming languages and frameworks commonly used in NLP and AI (e.g., Python, TensorFlow, PyTorch). * Excellent communication skills to collaborate effectively with cross-functional teams. * Demonstrated ability to lead projects independently and mentor technical teams. * A passion for staying up-to-date with the latest advancements in NLP and AI technologies. * Analytical thinker with great attention to detail. Medpace Overview Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries. Why Medpace? People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future. Medpace Perks * Flexible work environment * Competitive compensation and benefits package * Competitive PTO packages * Structured career paths with opportunities for professional growth * Company-sponsored employee appreciation events * Employee health and wellness initiatives Awards * Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 * Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility What To Expect Next A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps. EO/AA Employer M/F/Disability/Vets

Do you have a passion for Artificial Intelligence (AI) and looking to make a difference in how the latest clinical trials that can support new more personalised drugs progress into the market?Do you want to work in London with a great young vibe or do you prefer to work remote with a team of eager colleagues looking to make a difference in AI across the whole company? Medpace is open to those individuals passionate about AI wherever they are based in the UK.Do you have a background in data science and/or computer science with a run of working on AI projects and tools from Natural Language Processing (NLP) to Intelligent Automation (IA) to trying and training of Large Language Models (LLMs) for interactive AI applications across various IT systems? Have you worked with your IT colleagues to build out new AI applications that help users apply AI in their every day lives?Do you want to be using the latest AI tools and working on use cases that can be built into the latest deployed apps to make a difference in clinical trials? If so, we have an exciting opportunity for you to help take the reins of a groundbreaking project at Medpace.We are currently seeking a professional with direct experience interacting with artificial intelligence (AI) tools such as NLP, LLM, IA etc. Skills and training in natural language processing (NLP) and deep learning will be critical for this role. This professional will be expected to lead the programming and fine-tuning of various AI tools and helping the IT team to implement them into new applications. This professional will work collaboratively across the organisation with multiple teams to help design the roadmap for how AI can improve efficiency of company processes and provide insights and assistance to users. Applicants should have sufficient technical skills to help lead these types of AI projects independently and to train technical teams for support.Responsibilities * Research the latest AI tools from NLP to LLM to multi-agent capabilities to ensure we are maintaining a clear direction on the best in class AI; * Support the build and Implementation of private, large language models, fine-tuned based on both structured and text-based data inputs; * Integrate artificial intelligence to support AI applications that interact with the various AI tools through capabilities such as APIs; * Contribute to data and AI architecture review discussions, and support structural changes as needed; * Help drive AI technology thinking within the company across all departments; * Support departmental process improvement initiatives; and * Participate in educating, training and development of more junior team members.      Qualifications * Masters or PhD in engineering, computer or data science, or related field. * Proven experience implementing and fine-tuning Large Language Models or interactive AI applications (either >1 year post-graduate experience, or PhD dissertation experience). * Strong background in Natural Language Processing (NLP) and deep learning. * Preferably several years of experience working with different AI capabilities and showcasing your passion both at work and outside work in the utilization of AI. * Technical proficiency in programming languages and frameworks commonly used in NLP and AI (e.g., Python, TensorFlow, PyTorch). * Excellent communication skills to collaborate effectively with cross-functional teams. * Demonstrated ability to lead projects independently and mentor technical teams. * A passion for staying up-to-date with the latest advancements in NLP and AI technologies. * Analytical thinker with great attention to detail.      Medpace OverviewMedpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.Why Medpace?People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.Medpace Perks * Flexible work environment * Competitive compensation and benefits package * Competitive PTO packages * Structured career paths with opportunities for professional growth * Company-sponsored employee appreciation events * Employee health and wellness initiatives      Awards * Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 * Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility      What To Expect NextA Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.EO/AA Employer M/F/Disability/Vets

AI Specialist - Medpace

Do you have a passion for Artificial Intelligence (AI) and looking to make a difference in how the latest clinical trials that can support new more personalised drugs progress into the market?&lt;br&gt;&lt;br&gt;Do you want to work in London with a great young vibe or do you prefer to work remote with a team of eager colleagues looking to make a difference in AI across the whole company? Medpace is open to those individuals passionate about AI wherever they are based in the UK.&lt;br&gt;&lt;br&gt;Do you have a background in data science and/or computer science with a run of working on AI projects and tools from Natural Language Processing (NLP) to Intelligent Automation (IA) to trying and training of Large Language Models (LLMs) for interactive AI applications across various IT systems? Have you worked with your IT colleagues to build out new AI applications that help users apply AI in their every day lives?&lt;br&gt;&lt;br&gt;Do you want to be using the latest AI tools and working on use cases that can be built into the latest deployed apps to make a difference in clinical trials? If so, we have an exciting opportunity for you to help take the reins of a groundbreaking project at Medpace.&lt;br&gt;&lt;br&gt;We are currently seeking a professional with direct experience interacting with artificial intelligence (AI) tools such as NLP, LLM, IA etc. Skills and training in natural language processing (NLP) and deep learning will be critical for this role. This professional will be expected to lead the programming and fine-tuning of various AI tools and helping the IT team to implement them into new applications. This professional will work collaboratively across the organisation with multiple teams to help design the roadmap for how AI can improve efficiency of company processes and provide insights and assistance to users. Applicants should have sufficient technical skills to help lead these types of AI projects independently and to train technical teams for support.&lt;br&gt;&lt;br&gt;&lt;strong&gt;Responsibilities&lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;ul&gt;&lt;li&gt;Research the latest AI tools from NLP to LLM to multi-agent capabilities to ensure we are maintaining a clear direction on the best in class AI;&lt;/li&gt;&lt;li&gt;Support the build and Implementation of private, large language models, fine-tuned based on both structured and text-based data inputs;&lt;/li&gt;&lt;li&gt;Integrate artificial intelligence to support AI applications that interact with the various AI tools through capabilities such as APIs;&lt;/li&gt;&lt;li&gt;Contribute to data and AI architecture review discussions, and support structural changes as needed;&lt;/li&gt;&lt;li&gt;Help drive AI technology thinking within the company across all departments;&lt;/li&gt;&lt;li&gt;Support departmental process improvement initiatives; and&lt;/li&gt;&lt;li&gt;Participate in educating, training and development of more junior team members.&lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;&lt;strong&gt;Qualifications&lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;ul&gt;&lt;li&gt;Masters or PhD in engineering, computer or data science, or related field.&lt;/li&gt;&lt;li&gt;Proven experience implementing and fine-tuning Large Language Models or interactive AI applications (either &amp;gt;1 year post-graduate experience, or PhD dissertation experience).&lt;/li&gt;&lt;li&gt;Strong background in Natural Language Processing (NLP) and deep learning.&lt;/li&gt;&lt;li&gt;Preferably several years of experience working with different AI capabilities and showcasing your passion both at work and outside work in the utilization of AI.&lt;/li&gt;&lt;li&gt;Technical proficiency in programming languages and frameworks commonly used in NLP and AI (e.g., Python, TensorFlow, PyTorch).&lt;/li&gt;&lt;li&gt;Excellent communication skills to collaborate effectively with cross-functional teams.&lt;/li&gt;&lt;li&gt;Demonstrated ability to lead projects independently and mentor technical teams.&lt;/li&gt;&lt;li&gt;A passion for staying up-to-date with the latest advancements in NLP and AI technologies.&lt;/li&gt;&lt;li&gt;Analytical thinker with great attention to detail. &lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;&lt;strong&gt;Medpace Overview&lt;br&gt;&lt;br&gt;&lt;/strong&gt;Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.&lt;br&gt;&lt;br&gt;&lt;strong&gt;Why Medpace?&lt;br&gt;&lt;br&gt;&lt;/strong&gt;People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.&lt;br&gt;&lt;br&gt;The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.&lt;br&gt;&lt;br&gt;&lt;strong&gt;Medpace Perks&lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;ul&gt;&lt;li&gt;Flexible work environment &lt;/li&gt;&lt;li&gt;Competitive compensation and benefits package&lt;/li&gt;&lt;li&gt;Competitive PTO packages&lt;/li&gt;&lt;li&gt;Structured career paths with opportunities for professional growth&lt;/li&gt;&lt;li&gt;Company-sponsored employee appreciation events &lt;/li&gt;&lt;li&gt;Employee health and wellness initiatives&lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;&lt;strong&gt;Awards&lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;ul&gt;&lt;li&gt;Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024&lt;/li&gt;&lt;li&gt;Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility&lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;&lt;strong&gt;What To Expect Next&lt;br&gt;&lt;br&gt;&lt;/strong&gt;A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.&lt;br&gt;&lt;br&gt;EO/AA Employer M/F/Disability/Vets

AI Specialist

United Kingdom

You need a relevant bachelor's degree and 3 years of experience in clinical research or healthcare system administration, strong organizational skills, and familiarity with Microsoft Windows.

You will liaise between users and development teams, implement software approaches, interpret protocols, import data, ensure file format compliance, write tSQL queries, and perform system-related tasks.

Healthcare

Due to our continued growth, we are in search of qualified and focused individuals for a vital role in our Information Technology department. Our Clinical Application Administrator role works closely with multiple departments to help identify technical and user support issues of our internal software applications. This position will assist in troubleshooting, problem resolution and end user training. In addition, you will collaborate with our software engineers while providing exceptional support for both our internal and external users. Responsibilities * Act as a liaison between end users and application development teams while maintaining the interests of end users; * Develop and implement approaches for the use of software applications as they apply to individual users and study teams; * Interpret study protocols, protocol amendments, and other relevant operational documents for system set-up; * Import data between systems; * Work with internal and external users to ensure file formats meets systems requirements for to import data files; * Write tSQL queries to interact with reporting database when setting up data feeds and integrations, and * Perform other system-related tasks to meet company objectives. Qualifications * Bachelor's degree in Information Systems (or a related field) or Life Sciences and 3 years of experience in the clinical research industry or 3 years of experience as a system administration in a health care field; * Good organizational skills, very detail oriented, flexible, and possess good communication skills; * Ability to interact with staff and external users from multiple countries; * Must be able to work concurrently on several projects, each with specific requirements that may differ from project to project; * Demonstrated ability to learn new technologies/applications; * Familiar with field’s concepts, practices, and procedures; and * Knowledge of Microsoft® Windows operating systems. Medpace Overview Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries. Why Medpace? People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future. Medpace Perks * Flexible work environment * Competitive compensation and benefits package * Competitive PTO packages * Structured career paths with opportunities for professional growth * Company-sponsored employee appreciation events * Employee health and wellness initiatives Awards * Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 * Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility What To Expect Next A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps. EO/AA Employer M/F/Disability/Vets

Due to our continued growth, we are in search of qualified and focused individuals for a vital role in our Information Technology department. Our Clinical Application Administrator role works closely with multiple departments to help identify technical and user support issues of our internal software applications. This position will assist in troubleshooting, problem resolution and end user training. In addition, you will collaborate with our software engineers while providing exceptional support for both our internal and external users.Responsibilities * Act as a liaison between end users and application development teams while maintaining the interests of end users; * Develop and implement approaches for the use of software applications as they apply to individual users and study teams; * Interpret study protocols, protocol amendments, and other relevant operational documents for system set-up; * Import data between systems; * Work with internal and external users to ensure file formats meets systems requirements for to import data files; * Write tSQL queries to interact with reporting database when setting up data feeds and integrations, and * Perform other system-related tasks to meet company objectives.      Qualifications * Bachelor's degree in Information Systems (or a related field) or Life Sciences and 3 years of experience in the clinical research industry or 3 years of experience as a system administration in a health care field; * Good organizational skills, very detail oriented, flexible, and possess good communication skills; * Ability to interact with staff and external users from multiple countries; * Must be able to work concurrently on several projects, each with specific requirements that may differ from project to project; * Demonstrated ability to learn new technologies/applications; * Familiar with field’s concepts, practices, and procedures; and * Knowledge of Microsoft® Windows operating systems.      Medpace OverviewMedpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.Why Medpace?People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.Medpace Perks * Flexible work environment * Competitive compensation and benefits package * Competitive PTO packages * Structured career paths with opportunities for professional growth * Company-sponsored employee appreciation events * Employee health and wellness initiatives      Awards * Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 * Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility      What To Expect NextA Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.EO/AA Employer M/F/Disability/Vets

Clinical Application Administrator - Medpace

Due to our continued growth, we are in search of qualified and focused individuals for a vital role in our Information Technology department. Our Clinical Application Administrator role works closely with multiple departments to help identify technical and user support issues of our internal software applications. This position will assist in troubleshooting, problem resolution and end user training. In addition, you will collaborate with our software engineers while providing exceptional support for both our internal and external users.&lt;br&gt;&lt;br&gt;&lt;strong&gt;Responsibilities&lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;ul&gt;&lt;li&gt;Act as a liaison between end users and application development teams while maintaining the interests of end users; &lt;/li&gt;&lt;li&gt;Develop and implement approaches for the use of software applications as they apply to individual users and study teams;&lt;/li&gt;&lt;li&gt;Interpret study protocols, protocol amendments, and other relevant operational documents for system set-up;&lt;/li&gt;&lt;li&gt;Import data between systems;&lt;/li&gt;&lt;li&gt;Work with internal and external users to ensure file formats meets systems requirements for to import data files;&lt;/li&gt;&lt;li&gt;Write tSQL queries to interact with reporting database when setting up data feeds and integrations, and&lt;/li&gt;&lt;li&gt;Perform other system-related tasks to meet company objectives.&lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;&lt;strong&gt;Qualifications&lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;ul&gt;&lt;li&gt;Bachelor's degree in Information Systems (or a related field) or Life Sciences and 3 years of experience in the clinical research industry or 3 years of experience as a system administration in a health care field;&lt;/li&gt;&lt;li&gt;Good organizational skills, very detail oriented, flexible, and possess good communication skills;&lt;/li&gt;&lt;li&gt;Ability to interact with staff and external users from multiple countries;&lt;/li&gt;&lt;li&gt;Must be able to work concurrently on several projects, each with specific requirements that may differ from project to project;&lt;/li&gt;&lt;li&gt;Demonstrated ability to learn new technologies/applications;&lt;/li&gt;&lt;li&gt;Familiar with field’s concepts, practices, and procedures; and&lt;/li&gt;&lt;li&gt;Knowledge of Microsoft® Windows operating systems.&lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;&lt;strong&gt;Medpace Overview&lt;br&gt;&lt;br&gt;&lt;/strong&gt;Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.&lt;br&gt;&lt;br&gt;&lt;strong&gt;Why Medpace?&lt;br&gt;&lt;br&gt;&lt;/strong&gt;People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.&lt;br&gt;&lt;br&gt;The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.&lt;br&gt;&lt;br&gt;&lt;strong&gt;Medpace Perks&lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;ul&gt;&lt;li&gt;Flexible work environment &lt;/li&gt;&lt;li&gt;Competitive compensation and benefits package&lt;/li&gt;&lt;li&gt;Competitive PTO packages&lt;/li&gt;&lt;li&gt;Structured career paths with opportunities for professional growth&lt;/li&gt;&lt;li&gt;Company-sponsored employee appreciation events &lt;/li&gt;&lt;li&gt;Employee health and wellness initiatives&lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;&lt;strong&gt;Awards&lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;ul&gt;&lt;li&gt;Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024&lt;/li&gt;&lt;li&gt;Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility&lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;&lt;strong&gt;What To Expect Next&lt;br&gt;&lt;br&gt;&lt;/strong&gt;A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.&lt;br&gt;&lt;br&gt;EO/AA Employer M/F/Disability/Vets

Clinical Application Administrator

You need a minimum Bachelor’s in life sciences, 2+ years in Pharmacovigilance, safety database knowledge (Argus preferred), and familiarity with medical terminology and GCP guidelines.

You will collect and track SAE reports, generate safety documents, perform database entry and quality checks, lead project oversight, and train new coordinators on safety reporting.

At Medpace, our European Pharmacovigilance (PV) activities are growing rapidly. As such, we are searching for motivated individuals to join our Clinical Safety team in London. Working as part of a high performing group alongside Medical Monitors, Quality Assurance, Clinical Trial Management and others, this position plays a key role at Medpace to accomplish tasks and work on projects that are instrumental to the development of life changing medicines. If you want an exciting career where you can apply yourself to a variety of opportunities and develop new skills, then this is the opportunity for you! Responsibilities * Collect, process, and track serious adverse event (SAE) reports * Generate safety narratives and queries * Safety Database data entry * Perform quality control of safety cases * Generate Investigator Safety Letters * SAE reconciliation between safety database and clinical database * TMF uploads and quality control review * Preparation of clinical safety documents as required (i.e., safety management plan, periodic safety reports and presentations) * Attending internal and external meetings, as required (including sponsor TCs and audits/inspections) * Leading clinical trial projects (ensure client deliverables are met, provide oversight and compliance reports) Additional Responsibilities * Develop presentation material and present during face-to-face Sponsor meetings (i.e., Kick-off Meetings, Investigator Meetings) * Coordinate final medical review of study report narratives and submission to Medical Writers * Develop drafts of adjudication material (i.e., charter, reporting materials) * Provide periodic safety summaries to project Data Manager, Clinical Trial Manager, and Medical Monitor * Train new Clinical Safety Coordinators on safety reporting responsibilities * Coordinate safety responsibilities for aggregate reporting purposes (e.g., ensure timely data entry, tracking of pending cases, collaborate with Medical Monitor and Regulatory Affairs) Qualifications * Minimum Bachelor’s life science degree * 2+ years of Clinical Trial Pharmacovigilance experience * Working knowledge of Safety Databases (Argus is desirable) * Demonstrate advanced knowledge of medical terminology, global safety reporting requirements and Good Clinical Practice (GCP) Guidelines * Exposure to working on global trials as part of a multidisciplinary team Medpace Overview Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries. Why Medpace? People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future. Medpace Perks * Flexible work environment * Competitive compensation and benefits package * Competitive PTO packages * Structured career paths with opportunities for professional growth * Company-sponsored employee appreciation events * Employee health and wellness initiatives Awards * Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 * Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility What To Expect Next A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps. EO/AA Employer M/F/Disability/Vets

At Medpace, our European Pharmacovigilance (PV) activities are growing rapidly. As such, we are searching for motivated individuals to join our Clinical Safety team in London. Working as part of a high performing group alongside Medical Monitors, Quality Assurance, Clinical Trial Management and others, this position plays a key role at Medpace to accomplish tasks and work on projects that are instrumental to the development of life changing medicines. If you want an exciting career where you can apply yourself to a variety of opportunities and develop new skills, then this is the opportunity for you!Responsibilities * Collect, process, and track serious adverse event (SAE) reports * Generate safety narratives and queries * Safety Database data entry * Perform quality control of safety cases * Generate Investigator Safety Letters * SAE reconciliation between safety database and clinical database * TMF uploads and quality control review * Preparation of clinical safety documents as required (i.e., safety management plan, periodic safety reports and presentations) * Attending internal and external meetings, as required (including sponsor TCs and audits/inspections) * Leading clinical trial projects (ensure client deliverables are met, provide oversight and compliance reports)      Additional Responsibilities * Develop presentation material and present during face-to-face Sponsor meetings (i.e., Kick-off Meetings, Investigator Meetings) * Coordinate final medical review of study report narratives and submission to Medical Writers * Develop drafts of adjudication material (i.e., charter, reporting materials) * Provide periodic safety summaries to project Data Manager, Clinical Trial Manager, and Medical Monitor * Train new Clinical Safety Coordinators on safety reporting responsibilities * Coordinate safety responsibilities for aggregate reporting purposes (e.g., ensure timely data entry, tracking of pending cases, collaborate with Medical Monitor and Regulatory Affairs)      Qualifications * Minimum Bachelor’s life science degree * 2+ years of Clinical Trial Pharmacovigilance experience * Working knowledge of Safety Databases (Argus is desirable) * Demonstrate advanced knowledge of medical terminology, global safety reporting requirements and Good Clinical Practice (GCP) Guidelines * Exposure to working on global trials as part of a multidisciplinary team      Medpace OverviewMedpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.Why Medpace?People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.Medpace Perks * Flexible work environment * Competitive compensation and benefits package * Competitive PTO packages * Structured career paths with opportunities for professional growth * Company-sponsored employee appreciation events * Employee health and wellness initiatives      Awards * Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 * Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility      What To Expect NextA Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.EO/AA Employer M/F/Disability/Vets

Clinical Safety Coordinator - Pharmacovigilance / Drug Safety - Medpace

At Medpace, our European Pharmacovigilance (PV) activities are growing rapidly. As such, we are searching for motivated individuals to join our Clinical Safety team in London. Working as part of a high performing group alongside Medical Monitors, Quality Assurance, Clinical Trial Management and others, this position plays a key role at Medpace to accomplish tasks and work on projects that are instrumental to the development of life changing medicines. If you want an exciting career where you can apply yourself to a variety of opportunities and develop new skills, then this is the opportunity for you!&lt;br&gt;&lt;br&gt;&lt;strong&gt;Responsibilities&lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;ul&gt;&lt;li&gt;Collect, process, and track serious adverse event (SAE) reports&lt;/li&gt;&lt;li&gt;Generate safety narratives and queries&lt;/li&gt;&lt;li&gt;Safety Database data entry&lt;/li&gt;&lt;li&gt;Perform quality control of safety cases&lt;/li&gt;&lt;li&gt;Generate Investigator Safety Letters&lt;/li&gt;&lt;li&gt;SAE reconciliation between safety database and clinical database&lt;/li&gt;&lt;li&gt;TMF uploads and quality control review&lt;/li&gt;&lt;li&gt;Preparation of clinical safety documents as required (i.e., safety management plan, periodic safety reports and presentations)&lt;/li&gt;&lt;li&gt;Attending internal and external meetings, as required (including sponsor TCs and audits/inspections)&lt;/li&gt;&lt;li&gt;Leading clinical trial projects (ensure client deliverables are met, provide oversight and compliance reports)&lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;&lt;strong&gt;Additional Responsibilities&lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;ul&gt;&lt;li&gt;Develop presentation material and present during face-to-face Sponsor meetings (i.e., Kick-off Meetings, Investigator Meetings)&lt;/li&gt;&lt;li&gt;Coordinate final medical review of study report narratives and submission to Medical Writers&lt;/li&gt;&lt;li&gt;Develop drafts of adjudication material (i.e., charter, reporting materials)&lt;/li&gt;&lt;li&gt;Provide periodic safety summaries to project Data Manager, Clinical Trial Manager, and Medical Monitor&lt;/li&gt;&lt;li&gt;Train new Clinical Safety Coordinators on safety reporting responsibilities&lt;/li&gt;&lt;li&gt;Coordinate safety responsibilities for aggregate reporting purposes (e.g., ensure timely data entry, tracking of pending cases, collaborate with Medical Monitor and Regulatory Affairs)&lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;&lt;strong&gt;Qualifications&lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;ul&gt;&lt;li&gt;Minimum Bachelor’s life science degree&lt;/li&gt;&lt;li&gt;2+ years of Clinical Trial Pharmacovigilance experience&lt;/li&gt;&lt;li&gt;Working knowledge of Safety Databases (Argus is desirable)&lt;/li&gt;&lt;li&gt;Demonstrate advanced knowledge of medical terminology, global safety reporting requirements and Good Clinical Practice (GCP) Guidelines&lt;/li&gt;&lt;li&gt;Exposure to working on global trials as part of a multidisciplinary team&lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;&lt;strong&gt;Medpace Overview&lt;br&gt;&lt;br&gt;&lt;/strong&gt;Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.&lt;br&gt;&lt;br&gt;&lt;strong&gt;Why Medpace?&lt;br&gt;&lt;br&gt;&lt;/strong&gt;People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.&lt;br&gt;&lt;br&gt;The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.&lt;br&gt;&lt;br&gt;&lt;strong&gt;Medpace Perks&lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;ul&gt;&lt;li&gt;Flexible work environment &lt;/li&gt;&lt;li&gt;Competitive compensation and benefits package&lt;/li&gt;&lt;li&gt;Competitive PTO packages&lt;/li&gt;&lt;li&gt;Structured career paths with opportunities for professional growth&lt;/li&gt;&lt;li&gt;Company-sponsored employee appreciation events &lt;/li&gt;&lt;li&gt;Employee health and wellness initiatives&lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;&lt;strong&gt;Awards&lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;ul&gt;&lt;li&gt;Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024&lt;/li&gt;&lt;li&gt;Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility&lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;&lt;strong&gt;What To Expect Next&lt;br&gt;&lt;br&gt;&lt;/strong&gt;A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.&lt;br&gt;&lt;br&gt;EO/AA Employer M/F/Disability/Vets

Clinical Safety Coordinator - Pharmacovigilance / Drug Safety

You need a Bachelor's in Finance/Business/Accounting, 3+ years in clinical research or contract management, strong finance skills, basic medical knowledge, and advanced Excel abilities.

You will develop fee estimates, manage proposal texts, communicate with clients, track project budgets, review invoices, and build relationships to drive new business opportunities.

Accounting & Tax

Business, Operations & Strategy

Munich

Medpace is seeking office-based experienced finance or accounting professionals to join the Account Management department. These individuals will partner with clients and Medpace internal staff to develop project financial budgets and new business proposals. Senior Finance Account Analysts will work directly with clients to partner in strategic budget development to meet both their needs and those of Medpace. Responsibilities * Development of fee estimates for requests for proposals (RFPs), budget revisions, and contract amendments; * Provides financial input for response to requests for information (RFIs), and ensures coordination of all information with other relevant Medpace personnel as required; * Understand existing customer or potential customer’s business, pipeline, and opportunities in order to approach customer with confidence and knowledge; * Responsible for assuring that bid meets customer’s expectations and specific requirements; * Have thorough knowledge of Medpace bid process; * Review proposal text assumptions to ensure the fee estimate and proposal text assumptions are consistent; * Communicates with Medpace customers regarding ongoing projects to ensure customer’s expectations are being met; * Maintain and track ongoing performance of project against budget and notify internal and external clients when potential issues or changes are noted; * Review invoices and other financial reports prior to Sponsors receipt; * Build relationships within customer’s organization in order to generate new business opportunities and to develop partnership atmosphere; * Generate and initiate processing of new contracts and monitor/report on changes in scope, milestone invoicing and/or contract modification to all ongoing contracts in coordination with other employees; * Maintain and modify company bid preparation template and boilerplate text to meet changing client needs or specific requirements; * May be responsible for other projects and responsibilities as assigned. Qualifications * Bachelor's Degree in Finance, Business or Accounting; * 3+ years of experience in the conduct of clinical research and/or contract management/pricing; * Strong working knowledge of financial and accounting processes; * Basic knowledge of medical terminology and a working knowledge of drug development services desired; * Excellent analytical, written and oral communication skills; and * Excellent computer skills, especially a strong knowledge of Microsoft Excel. Medpace Overview Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries. Why Medpace? People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future. Medpace Perks * Flexible work environment * Competitive compensation and benefits package * Competitive PTO packages * Structured career paths with opportunities for professional growth * Company-sponsored employee appreciation events * Employee health and wellness initiatives Awards * Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 * Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility What To Expect Next A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps. EO/AA Employer M/F/Disability/Vets

Medpace is seeking office-based experienced finance or accounting professionals to join the Account Management department. These individuals will partner with clients and Medpace internal staff to develop project financial budgets and new business proposals. Senior Finance Account Analysts will work directly with clients to partner in strategic budget development to meet both their needs and those of Medpace.Responsibilities * Development of fee estimates for requests for proposals (RFPs), budget revisions, and contract amendments; * Provides financial input for response to requests for information (RFIs), and ensures coordination of all information with other relevant Medpace personnel as required; * Understand existing customer or potential customer’s business, pipeline, and opportunities in order to approach customer with confidence and knowledge; * Responsible for assuring that bid meets customer’s expectations and specific requirements; * Have thorough knowledge of Medpace bid process; * Review proposal text assumptions to ensure the fee estimate and proposal text assumptions are consistent; * Communicates with Medpace customers regarding ongoing projects to ensure customer’s expectations are being met; * Maintain and track ongoing performance of project against budget and notify internal and external clients when potential issues or changes are noted; * Review invoices and other financial reports prior to Sponsors receipt; * Build relationships within customer’s organization in order to generate new business opportunities and to develop partnership atmosphere; * Generate and initiate processing of new contracts and monitor/report on changes in scope, milestone invoicing and/or contract modification to all ongoing contracts in coordination with other employees; * Maintain and modify company bid preparation template and boilerplate text to meet changing client needs or specific requirements; * May be responsible for other projects and responsibilities as assigned.      Qualifications * Bachelor's Degree in Finance, Business or Accounting; * 3+ years of experience in the conduct of clinical research and/or contract management/pricing; * Strong working knowledge of financial and accounting processes; * Basic knowledge of medical terminology and a working knowledge of drug development services desired; * Excellent analytical, written and oral communication skills; and * Excellent computer skills, especially a strong knowledge of Microsoft Excel.      Medpace OverviewMedpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.Why Medpace?People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.Medpace Perks * Flexible work environment * Competitive compensation and benefits package * Competitive PTO packages * Structured career paths with opportunities for professional growth * Company-sponsored employee appreciation events * Employee health and wellness initiatives      Awards * Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 * Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility      What To Expect NextA Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.EO/AA Employer M/F/Disability/Vets

Senior Commercial Finance Analyst - Medpace

Medpace is seeking office-based experienced finance or accounting professionals to join the Account Management department. These individuals will partner with clients and Medpace internal staff to develop project financial budgets and new business proposals. Senior Finance Account Analysts will work directly with clients to partner in strategic budget development to meet both their needs and those of Medpace.&lt;br&gt;&lt;br&gt;&lt;strong&gt;Responsibilities&lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;ul&gt;&lt;li&gt;Development of fee estimates for requests for proposals (RFPs), budget revisions, and contract amendments;&lt;/li&gt;&lt;li&gt;Provides financial input for response to requests for information (RFIs), and ensures coordination of all information with other relevant Medpace personnel as required;&lt;/li&gt;&lt;li&gt;Understand existing customer or potential customer’s business, pipeline, and opportunities in order to approach customer with confidence and knowledge;&lt;/li&gt;&lt;li&gt;Responsible for assuring that bid meets customer’s expectations and specific requirements;&lt;/li&gt;&lt;li&gt;Have thorough knowledge of Medpace bid process;&lt;/li&gt;&lt;li&gt;Review proposal text assumptions to ensure the fee estimate and proposal text assumptions are consistent;&lt;/li&gt;&lt;li&gt;Communicates with Medpace customers regarding ongoing projects to ensure customer’s expectations are being met;&lt;/li&gt;&lt;li&gt;Maintain and track ongoing performance of project against budget and notify internal and external clients when potential issues or changes are noted;&lt;/li&gt;&lt;li&gt;Review invoices and other financial reports prior to Sponsors receipt;&lt;/li&gt;&lt;li&gt;Build relationships within customer’s organization in order to generate new business opportunities and to develop partnership atmosphere;&lt;/li&gt;&lt;li&gt;Generate and initiate processing of new contracts and monitor/report on changes in scope, milestone invoicing and/or contract modification to all ongoing contracts in coordination with other employees;&lt;/li&gt;&lt;li&gt;Maintain and modify company bid preparation template and boilerplate text to meet changing client needs or specific requirements;&lt;/li&gt;&lt;li&gt;May be responsible for other projects and responsibilities as assigned.&lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;&lt;strong&gt;Qualifications&lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;ul&gt;&lt;li&gt;Bachelor's Degree in Finance, Business or Accounting;&lt;/li&gt;&lt;li&gt;3+ years of experience in the conduct of clinical research and/or contract management/pricing;&lt;/li&gt;&lt;li&gt;Strong working knowledge of financial and accounting processes;&lt;/li&gt;&lt;li&gt;Basic knowledge of medical terminology and a working knowledge of drug development services desired;&lt;/li&gt;&lt;li&gt;Excellent analytical, written and oral communication skills; and&lt;/li&gt;&lt;li&gt;Excellent computer skills, especially a strong knowledge of Microsoft Excel.&lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;&lt;strong&gt;Medpace Overview&lt;br&gt;&lt;br&gt;&lt;/strong&gt;Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.&lt;br&gt;&lt;br&gt;&lt;strong&gt;Why Medpace?&lt;br&gt;&lt;br&gt;&lt;/strong&gt;People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.&lt;br&gt;&lt;br&gt;The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.&lt;br&gt;&lt;br&gt;&lt;strong&gt;Medpace Perks&lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;ul&gt;&lt;li&gt;Flexible work environment &lt;/li&gt;&lt;li&gt;Competitive compensation and benefits package&lt;/li&gt;&lt;li&gt;Competitive PTO packages&lt;/li&gt;&lt;li&gt;Structured career paths with opportunities for professional growth&lt;/li&gt;&lt;li&gt;Company-sponsored employee appreciation events &lt;/li&gt;&lt;li&gt;Employee health and wellness initiatives&lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;&lt;strong&gt;Awards&lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;ul&gt;&lt;li&gt;Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024&lt;/li&gt;&lt;li&gt;Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility&lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;&lt;strong&gt;What To Expect Next&lt;br&gt;&lt;br&gt;&lt;/strong&gt;A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.&lt;br&gt;&lt;br&gt;EO/AA Employer M/F/Disability/Vets

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Juno: flexible benefits, limitless possibilities®

MyEyeDr.

University Hospitals Sussex NHS Foundation Trust (279)

Androlabs®

IWK Health Centre

PHSA

SCA Health

Vets Now

North Bristol NHS Trust

Liverpool University Hospitals NHS Foundation Trust