Large

We are creative thinkers with decades of clinical trial experience who drive innovative solutions powered by insights from data and technology. As we tackle challenges in today’s world, we know that we need to be nimble and agile. That’s why we work side-by-side with our partners to eliminate inefficiencies from the process so we can help them deliver life-changing therapies faster for patients, caregivers and healthcare providers worldwide.

Science & Healthcare

Fortrea

Healthcare

You need a bachelor’s degree or equivalent, strong organizational and project management skills, traffic and paid media experience, excellent communication, and analytical skills. PMP preferred.

You will support marketing initiatives, manage events, track media plans, create purchase orders, build project plans, collaborate with departments, and ensure timely execution of tasks.

Marketing

Reading

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access, and technology solutions across more than 20 therapeutic areas. Conducting operations in more than 90 countries, Fortrea is transforming drug and device development for partners and patients across the globe.<br><br>We are seeking a highly organized Marketing Project Coordinator to manage multiple marketing projects, ensuring the delivery of high-quality outcomes while meeting deadlines and budget objectives. The role involves coordinating and tracking various marketing programs, including email, event, social media, and content marketing initiatives. This individual will support the marketing team by overseeing logistics for events, managing media plans, and ensuring smooth execution of marketing campaigns.<br><br>A key requirement for this role is traffic experience, ideally gained in an advertising agency or similar environment. This includes managing the flow of tasks, coordinating with different teams to ensure timely and efficient project completion, and improving processes. The ideal candidate will also have experience with paid media planning, strong project management skills, and a keen attention to detail. Excellent communication and time management abilities are essential, as well as a strong grasp of various marketing platforms and channels.<br><br>Summary of Responsibilities:<br><br><br> * Support the marketing department's initiatives with the planning, executing, and tracking of marketing programs such as email, event, social media, or content marketing<br> * Create and manage purchase orders on behalf of the marketing team.<br> * Track and support execution of media plans in collaboration with Executive Director Brand Marketing.<br> * Independently coordinate marketing and community events, including overseeing logistics, managing registrations, coordinating with vendors, creating itineraries, and ordering marketing collateral<br> * Build project management plans, track progress and report metrics of marketing initiatives.<br> * Collaborate with stakeholders across departments to understand data needs and requirements.<br> * Strong attention to detail with an analytical mind and outstanding problem-solving skills.<br> * Strong communication, presentation, and storytelling skills<br> * Fantastic time management skills with the ability to multi-task.<br> * All other duties as needed or assigned.<br>   <br>   <br>   <br><br>Qualifications/Experience:<br><br><br> * Bachelor's degree or equivalent and relevant formal academic qualification. Fortrea may consider relevant and equivalent experience in lieu of educational requirements.<br> * Must have strong organizational and project management skills, as well as attention to detail<br> * Traffic experience from an advertising agency or equivalent<br> * Paid media planning experience<br> * Excellent written and verbal communication skills, as well as outstanding copywriting and proofreading skills<br> * Firm grasp on various marketing platforms, channels, and best practices, including social, digital, and email marketing<br> * Must be a self-starter and able to independently move projects forward, prioritize tasks, and meet deadlines<br> * Must have strong analytical skills to analyze metrics and create reports<br> * Experience in job discipline<br>   <br>   <br>   <br><br>Preferred Qualifications Include:<br><br><br> * PMP certification preferred<br>   <br>   <br>   <br><br>Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. Join our exceptional team and embrace a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact. For more information about Fortrea, visit www.fortrea.com.<br><br>Fortrea is proud to be an Equal Opportunity Employer:<br><br>As an EOE/AA employer, Fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.<br><br>For more information about how we collect and store your personal data, please see our Privacy Statement.<br><br>

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access, and technology solutions across more than 20 therapeutic areas. Conducting operations in more than 90 countries, Fortrea is transforming drug and device development for partners and patients across the globe.We are seeking a highly organized Marketing Project Coordinator to manage multiple marketing projects, ensuring the delivery of high-quality outcomes while meeting deadlines and budget objectives. The role involves coordinating and tracking various marketing programs, including email, event, social media, and content marketing initiatives. This individual will support the marketing team by overseeing logistics for events, managing media plans, and ensuring smooth execution of marketing campaigns.A key requirement for this role is traffic experience, ideally gained in an advertising agency or similar environment. This includes managing the flow of tasks, coordinating with different teams to ensure timely and efficient project completion, and improving processes. The ideal candidate will also have experience with paid media planning, strong project management skills, and a keen attention to detail. Excellent communication and time management abilities are essential, as well as a strong grasp of various marketing platforms and channels.Summary of Responsibilities: * Support the marketing department's initiatives with the planning, executing, and tracking of marketing programs such as email, event, social media, or content marketing * Create and manage purchase orders on behalf of the marketing team. * Track and support execution of media plans in collaboration with Executive Director Brand Marketing. * Independently coordinate marketing and community events, including overseeing logistics, managing registrations, coordinating with vendors, creating itineraries, and ordering marketing collateral * Build project management plans, track progress and report metrics of marketing initiatives. * Collaborate with stakeholders across departments to understand data needs and requirements. * Strong attention to detail with an analytical mind and outstanding problem-solving skills. * Strong communication, presentation, and storytelling skills * Fantastic time management skills with the ability to multi-task. * All other duties as needed or assigned.         Qualifications/Experience: * Bachelor's degree or equivalent and relevant formal academic qualification. Fortrea may consider relevant and equivalent experience in lieu of educational requirements. * Must have strong organizational and project management skills, as well as attention to detail * Traffic experience from an advertising agency or equivalent * Paid media planning experience * Excellent written and verbal communication skills, as well as outstanding copywriting and proofreading skills * Firm grasp on various marketing platforms, channels, and best practices, including social, digital, and email marketing * Must be a self-starter and able to independently move projects forward, prioritize tasks, and meet deadlines * Must have strong analytical skills to analyze metrics and create reports * Experience in job discipline         Preferred Qualifications Include: * PMP certification preferred         Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. Join our exceptional team and embrace a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact. For more information about Fortrea, visit www.fortrea.com.Fortrea is proud to be an Equal Opportunity Employer:As an EOE/AA employer, Fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.For more information about how we collect and store your personal data, please see our Privacy Statement.

Marketing Coordinator - Fortrea

Maidenhead, England, United Kingdom

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access, and technology solutions across more than 20 therapeutic areas. Conducting operations in more than 90 countries, Fortrea is transforming drug and device development for partners and patients across the globe.&lt;br&gt;&lt;br&gt;We are seeking a highly organized &lt;strong&gt;Marketing Project Coordinator&lt;/strong&gt; to manage multiple marketing projects, ensuring the delivery of high-quality outcomes while meeting deadlines and budget objectives. The role involves coordinating and tracking various marketing programs, including email, event, social media, and content marketing initiatives. This individual will support the marketing team by overseeing logistics for events, managing media plans, and ensuring smooth execution of marketing campaigns.&lt;br&gt;&lt;br&gt;A key requirement for this role is &lt;strong&gt;traffic experience&lt;/strong&gt;, ideally gained in an advertising agency or similar environment. This includes managing the flow of tasks, coordinating with different teams to ensure timely and efficient project completion, and improving processes. The ideal candidate will also have experience with paid media planning, strong project management skills, and a keen attention to detail. Excellent communication and time management abilities are essential, as well as a strong grasp of various marketing platforms and channels.&lt;br&gt;&lt;br&gt;&lt;strong&gt;Summary of Responsibilities:&lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;ul&gt;&lt;li&gt;Support the marketing department's initiatives with the planning, executing, and tracking of marketing programs such as email, event, social media, or content marketing&lt;/li&gt;&lt;li&gt;Create and manage purchase orders on behalf of the marketing team.&lt;/li&gt;&lt;li&gt;Track and support execution of media plans in collaboration with Executive Director Brand Marketing.&lt;/li&gt;&lt;li&gt;Independently coordinate marketing and community events, including overseeing logistics, managing registrations, coordinating with vendors, creating itineraries, and ordering marketing collateral&lt;/li&gt;&lt;li&gt;Build project management plans, track progress and report metrics of marketing initiatives.&lt;/li&gt;&lt;li&gt;Collaborate with stakeholders across departments to understand data needs and requirements.&lt;/li&gt;&lt;li&gt;Strong attention to detail with an analytical mind and outstanding problem-solving skills.&lt;/li&gt;&lt;li&gt;Strong communication, presentation, and storytelling skills&lt;/li&gt;&lt;li&gt;Fantastic time management skills with the ability to multi-task.&lt;/li&gt;&lt;li&gt;All other duties as needed or assigned.&lt;br&gt;&lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;&lt;strong&gt;Qualifications/Experience:&lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;ul&gt;&lt;li&gt;Bachelor's degree or equivalent and relevant formal academic qualification. Fortrea may consider relevant and equivalent experience in lieu of educational requirements.&lt;/li&gt;&lt;li&gt;Must have strong organizational and project management skills, as well as attention to detail&lt;/li&gt;&lt;li&gt;Traffic experience from an advertising agency or equivalent&lt;/li&gt;&lt;li&gt;Paid media planning experience&lt;/li&gt;&lt;li&gt;Excellent written and verbal communication skills, as well as outstanding copywriting and proofreading skills&lt;/li&gt;&lt;li&gt;Firm grasp on various marketing platforms, channels, and best practices, including social, digital, and email marketing&lt;/li&gt;&lt;li&gt;Must be a self-starter and able to independently move projects forward, prioritize tasks, and meet deadlines&lt;/li&gt;&lt;li&gt;Must have strong analytical skills to analyze metrics and create reports&lt;/li&gt;&lt;li&gt;Experience in job discipline&lt;br&gt;&lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;&lt;strong&gt;Preferred Qualifications Include:&lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;ul&gt;&lt;li&gt;PMP certification preferred&lt;br&gt;&lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. Join our exceptional team and embrace a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact. For more information about Fortrea, visit www.fortrea.com.&lt;br&gt;&lt;br&gt;&lt;strong&gt;Fortrea is proud to be an Equal Opportunity Employer:&lt;br&gt;&lt;br&gt;&lt;/strong&gt;As an EOE/AA employer, Fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.&lt;br&gt;&lt;br&gt;For more information about how we collect and store your personal data, please see our Privacy Statement.&lt;br&gt;&lt;br&gt;

Marketing Coordinator

You must be pursuing a life/health sciences degree, manage multiple projects, prioritize effectively, meet deadlines, collaborate well, and have strong MS Office skills.

You will support project managers, coordinate teams, prepare documentation for Ethics Committees, manage project tools, facilitate meetings, and ensure accuracy in clinical trial documents.

Research & Development

Leeds

<div>
 <div>
  As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access, and technology solutions across more than 20 therapeutic areas. Conducting operations in more than 90 countries, Fortrea is transforming drug and device development for partners and patients across the globe.
 </div>
 <div>
  Fortrea 2025 University Internship Program<br> <br> Location: Remote in the UK, hybrid if you live in Leeds
 </div>
 <div>
  <br> Full-time, 12-month internship<br> <br> Start Date: July 2025
 </div>
 <div></div>
 <div>
  KICKSTART YOUR CAREER IN LIFE SCIENCES
 </div>
 <div>
  <br> Are you passionate about advancing the frontiers of medicine?
 </div>
 <div></div>
 <div>
  Launch your Life Sciences career with Fortrea’s one-year University Internship Program, designed to give students hands-on experience in the Healthcare and Clinical Research industries.
 </div>
 <div></div>
 <div>
  This internship will provide you with real-world insights into how new medicines are developed, offering exposure to the cutting-edge knowledge and processes driving modern Drug Development to bring new medicines to life.
 </div>
 <div></div>
 <div>
  WHAT YOU´LL DO
 </div>
 <div>
  <br> Over the course of 12 months, you’ll work closely with our Project Management team. You’ll be part of a 3-month rotation across four different teams, giving you a comprehensive understanding of how life-saving medicines begin their journey:
 </div>
 <div></div>
 <ul>
  <li>Project Management: Support our PMs in coordinating cross-functional teams to ensure operational excellence. You'll gain insight into managing timelines, risks, budgets, and achieving quality standards.</li>
 </ul>
 <div></div>
 <ul>
  <li>Study Start-Up: work hand-by-hand with our specialists to learn how to prepare and submit essential documentation for UK Ethics Committees approvals, allowing clinical trials to begin.<br></li>
  <li>Project Coordination: Help set up project management tools, professionally manage team meetings, and engage directly with clients to ensure smooth project operations.<br></li>
  <li>Clinical Trial Documentation: Perform quality checks on study-related documents, ensuring accuracy, and contribute to maintaining the electronic Trial Master File (eTMF).</li>
 </ul>
 <div></div>
 <div>
  WHY AN INTERNSHIP WITH FORTREA?
 </div>
 <div></div>
 <div>
  At Fortrea, you’ll gain more than just work experience—you’ll receive a wealth of knowledge, mentorship, and career guidance. Our internship is designed to develop your skills, broaden your understanding of clinical research, and prepare you for the next steps in your career.
 </div>
 <div></div>
 <div>
  Key Highlights of the Program:
 </div>
 <div></div>
 <ul>
  <li>Mentorship: Dedicated mentors to guide your journey.<br></li>
  <li>Learning Workshops: Access to program workshops and leadership speakers.<br></li>
  <li>Networking Opportunities: Connect with professionals through employee resource groups, panel discussions, and small group ‘coffee chats’.<br></li>
  <li>Real-World Experience: Work on actual projects from day one, contributing directly to clinical research outcomes and gaining valuable business acumen.</li>
 </ul>
 <div></div>
 <div>
  WHAT WE´RE LOOKING FOR<br>
 </div>
 <ul>
  <li>You must be currently pursuing an undergraduate degree in life or health sciences (commenced in 2023).</li>
  <li>Experience managing multiple projects in an academic or professional setting.</li>
  <li>Demonstrated ability to plan, multi-task and prioritize</li>
  <li>Ability to work to deadlines and to collaborate with various stakeholders in a fast-paced environment, where priorities can change rapidly and you have to adapt on the spot.</li>
  <li>Demonstrated computer skills – requires excellent MS Office experience (specifically Excel, Word, Outlook)</li>
  <li>Demonstrated teamwork, communication (written and verbal), and organizational skills</li>
 </ul>
 <div></div>
 <div>
  WHY THIS INTERNSHIP MATTERS
 </div>
 <div>
  <br> Joining Fortrea’s internship program is a unique opportunity to gain practical skills, industry knowledge, and professional connections that will set you up for future success. You’ll be immersed in the day-to-day workings of a global clinical research company, gaining invaluable experience and making a real impact on healthcare advancements.
 </div>
 <div></div>
 <div>
  APPLY TODAY<br> <br> Seize the chance to contribute to the future of healthcare while building a strong foundation for your career in life sciences. Apply now to join our 2025 University Internship Program!
 </div>
 <div>
  Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. Join our exceptional team and embrace a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact. For more information about Fortrea, visit www.fortrea.com.
 </div>
 <div></div>
 <div>
  Fortrea is proud to be an Equal Opportunity Employer:
 </div>
 <div>
  <br> As an EOE/AA employer, Fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.
 </div>
 <div></div>
 <div>
  For more information about how we collect and store your personal data, please see our 
  <div>
   Privacy Statement
  </div>.
 </div>
</div>


 
  As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access, and technology solutions across more than 20 therapeutic areas. Conducting operations in more than 90 countries, Fortrea is transforming drug and device development for partners and patients across the globe.
 
 
  Fortrea 2025 University Internship Program  Location: Remote in the UK, hybrid if you live in Leeds
 
 
   Full-time, 12-month internship  Start Date: July 2025
 
 
 
  KICKSTART YOUR CAREER IN LIFE SCIENCES
 
 
   Are you passionate about advancing the frontiers of medicine?
 
 
 
  Launch your Life Sciences career with Fortrea’s one-year University Internship Program, designed to give students hands-on experience in the Healthcare and Clinical Research industries.
 
 
 
  This internship will provide you with real-world insights into how new medicines are developed, offering exposure to the cutting-edge knowledge and processes driving modern Drug Development to bring new medicines to life.
 
 
 
  WHAT YOU´LL DO
 
 
   Over the course of 12 months, you’ll work closely with our Project Management team. You’ll be part of a 3-month rotation across four different teams, giving you a comprehensive understanding of how life-saving medicines begin their journey:
 
 
 
  Project Management: Support our PMs in coordinating cross-functional teams to ensure operational excellence. You'll gain insight into managing timelines, risks, budgets, and achieving quality standards.
 
 
 
  Study Start-Up: work hand-by-hand with our specialists to learn how to prepare and submit essential documentation for UK Ethics Committees approvals, allowing clinical trials to begin.
  Project Coordination: Help set up project management tools, professionally manage team meetings, and engage directly with clients to ensure smooth project operations.
  Clinical Trial Documentation: Perform quality checks on study-related documents, ensuring accuracy, and contribute to maintaining the electronic Trial Master File (eTMF).
 
 
 
  WHY AN INTERNSHIP WITH FORTREA?
 
 
 
  At Fortrea, you’ll gain more than just work experience—you’ll receive a wealth of knowledge, mentorship, and career guidance. Our internship is designed to develop your skills, broaden your understanding of clinical research, and prepare you for the next steps in your career.
 
 
 
  Key Highlights of the Program:
 
 
 
  Mentorship: Dedicated mentors to guide your journey.
  Learning Workshops: Access to program workshops and leadership speakers.
  Networking Opportunities: Connect with professionals through employee resource groups, panel discussions, and small group ‘coffee chats’.
  Real-World Experience: Work on actual projects from day one, contributing directly to clinical research outcomes and gaining valuable business acumen.
 
 
 
  WHAT WE´RE LOOKING FOR
 
 
  You must be currently pursuing an undergraduate degree in life or health sciences (commenced in 2023).
  Experience managing multiple projects in an academic or professional setting.
  Demonstrated ability to plan, multi-task and prioritize
  Ability to work to deadlines and to collaborate with various stakeholders in a fast-paced environment, where priorities can change rapidly and you have to adapt on the spot.
  Demonstrated computer skills – requires excellent MS Office experience (specifically Excel, Word, Outlook)
  Demonstrated teamwork, communication (written and verbal), and organizational skills
 
 
 
  WHY THIS INTERNSHIP MATTERS
 
 
   Joining Fortrea’s internship program is a unique opportunity to gain practical skills, industry knowledge, and professional connections that will set you up for future success. You’ll be immersed in the day-to-day workings of a global clinical research company, gaining invaluable experience and making a real impact on healthcare advancements.
 
 
 
  APPLY TODAY  Seize the chance to contribute to the future of healthcare while building a strong foundation for your career in life sciences. Apply now to join our 2025 University Internship Program!
 
 
  Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. Join our exceptional team and embrace a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact. For more information about Fortrea, visit www.fortrea.com.
 
 
 
  Fortrea is proud to be an Equal Opportunity Employer:
 
 
   As an EOE/AA employer, Fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.
 
 
 
  For more information about how we collect and store your personal data, please see our 
  
   Privacy Statement
  .
 


Project Management, 2025 12-month Internship - Fortrea

Project Management, 2025 12-month Internship

You must pursue a life/health sciences degree, manage multiple projects, meet deadlines, adapt in fast-paced environments, and have strong MS Office, teamwork, and communication skills.

You will interact with participants, conduct assessments, monitor vitals, perform ECGs, manage screening appointments, and process laboratory samples with training provided.

<div>
 <div>
  As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access, and technology solutions across more than 20 therapeutic areas. Conducting operations in more than 90 countries, Fortrea is transforming drug and device development for partners and patients across the globe.
 </div>
 <div>
  Where to start when your passion is expanding the frontiers of medicine?
 </div>
 <div></div>
 <div>
  Launch an international career with Fortrea´s one-year University Internship Program
 </div>
 <div></div>
 <div>
  Full time. Leeds. Start Date: July 2025
 </div>
 <div></div>
 <div>
  Fortrea’s 2025 internships offer students pursuing a Bachelor's degree in life sciences the hands-on experience needed to confidently launch a successful career in the fields of Life Sciences, Healthcare, and Clinical Research. You'll gain real-world insights into the cutting-edge knowledge and processes driving modern Drug Development to bring new medicines to life.
 </div>
 <div></div>
 <div>
  FORTREA LEEDS – WHERE BREAKTHROUGHS BEGIN
 </div>
 <div></div>
 <div>
  This internship has been designed to give you comprehensive look into Early Clinical Research at our state-of-the-art, 65,000 ft² Clinical Research Clinic in Drapers Yard, Leeds—just a 7-minute walk from the train station.
 </div>
 <div></div>
 <div>
  You'll experience firsthand how life-saving medicines begin their journey through a 4-month rotation system across 3 different teams, providing an excellent introduction to Phase I clinical trials:
 </div>
 <div></div>
 <div>
  Clinical Operations – After a deep training and working alongside the clinical operations team, you´ll directly interact with patients and healthy volunteers, responsible for tasks such as taking bloods, monitoring vital signs, conducting ECGs and other study assessment as required.
 </div>
 <div></div>
 <div>
  Screening – Gain a comprehensive understanding of the screening process required for a volunteer to be accepted onto a Phase I study. We provide full training to conduct screening appointments, including completing assessments and entering data into the electronic data capture system.
 </div>
 <div></div>
 <div>
  Laboratory – Join the laboratory technician team and learn how to process, pipette, store and ship the samples required to complete a Phase I study. Full training is provided in all aspects of laboratory work.
 </div>
 <div></div>
 <div>
  WHY AN INTERNSHIP WITH FORTREA?
 </div>
 <div></div>
 <div>
  Varied suit of learning methods to support your development and career exploration:
 </div>
 <ul>
  <li>Dedicated mentors</li>
  <li>Program workshops</li>
  <li>Leadership speakers</li>
  <li>Employee Resource Groups</li>
  <li>Panel discussions</li>
  <li>Small group ‘coffee chats’</li>
 </ul>
 <div>
  <br> Gain business acumen: You will compliment your education working on actual department assignments, learning how our company operates while gaining insights into scientific and business processes. All of this will give you an understanding of the complexities of the clinical research industry.
 </div>
 <div></div>
 <div>
  Learn from Day One: Embrace a hands-on learning experience from the moment you step in the door. You won't just be an observer, but an active part of the team, contributing to get study data in real-time, gaining practical insights and real-world skills.
 </div>
 <div></div>
 <div>
  EDUCATION/QUALIFICATIONS
 </div>
 <div></div>
 <ul>
  <li>You must be currently pursuing an undergraduate degree (started in the academic year of 2023) in any of the life or health sciences.</li>
  <li>Experience delivering multiple projects in an academic or professional setting.</li>
  <li>Demonstrated ability to plan, multi-task and prioritize</li>
  <li>Ability to work to deadlines</li>
  <li>Ability to collaborate with various stakeholders in a fast-paced environment, where priorities can change rapidly and you have to adapt on the spot.</li>
  <li>Demonstrated computer skills – requires excellent MS Office experience (specifically Excel, Word, Outlook)</li>
  <li>Demonstrated teamwork, communication (written and verbal), and organizational skills</li>
 </ul>
 <div></div>
 <div>
  Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. Join our exceptional team and embrace a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact. For more information about Fortrea, visit www.fortrea.com.
 </div>
 <div></div>
 <div>
  Fortrea is proud to be an Equal Opportunity Employer:
 </div>
 <div>
  <br> As an EOE/AA employer, Fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.
 </div>
 <div></div>
 <div>
  For more information about how we collect and store your personal data, please see our 
  <div>
   Privacy Statement
  </div>.
 </div>
</div>


 
  As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access, and technology solutions across more than 20 therapeutic areas. Conducting operations in more than 90 countries, Fortrea is transforming drug and device development for partners and patients across the globe.
 
 
  Where to start when your passion is expanding the frontiers of medicine?
 
 
 
  Launch an international career with Fortrea´s one-year University Internship Program
 
 
 
  Full time. Leeds. Start Date: July 2025
 
 
 
  Fortrea’s 2025 internships offer students pursuing a Bachelor's degree in life sciences the hands-on experience needed to confidently launch a successful career in the fields of Life Sciences, Healthcare, and Clinical Research. You'll gain real-world insights into the cutting-edge knowledge and processes driving modern Drug Development to bring new medicines to life.
 
 
 
  FORTREA LEEDS – WHERE BREAKTHROUGHS BEGIN
 
 
 
  This internship has been designed to give you comprehensive look into Early Clinical Research at our state-of-the-art, 65,000 ft² Clinical Research Clinic in Drapers Yard, Leeds—just a 7-minute walk from the train station.
 
 
 
  You'll experience firsthand how life-saving medicines begin their journey through a 4-month rotation system across 3 different teams, providing an excellent introduction to Phase I clinical trials:
 
 
 
  Clinical Operations – After a deep training and working alongside the clinical operations team, you´ll directly interact with patients and healthy volunteers, responsible for tasks such as taking bloods, monitoring vital signs, conducting ECGs and other study assessment as required.
 
 
 
  Screening – Gain a comprehensive understanding of the screening process required for a volunteer to be accepted onto a Phase I study. We provide full training to conduct screening appointments, including completing assessments and entering data into the electronic data capture system.
 
 
 
  Laboratory – Join the laboratory technician team and learn how to process, pipette, store and ship the samples required to complete a Phase I study. Full training is provided in all aspects of laboratory work.
 
 
 
  WHY AN INTERNSHIP WITH FORTREA?
 
 
 
  Varied suit of learning methods to support your development and career exploration:
 
 
  Dedicated mentors
  Program workshops
  Leadership speakers
  Employee Resource Groups
  Panel discussions
  Small group ‘coffee chats’
 
 
   Gain business acumen: You will compliment your education working on actual department assignments, learning how our company operates while gaining insights into scientific and business processes. All of this will give you an understanding of the complexities of the clinical research industry.
 
 
 
  Learn from Day One: Embrace a hands-on learning experience from the moment you step in the door. You won't just be an observer, but an active part of the team, contributing to get study data in real-time, gaining practical insights and real-world skills.
 
 
 
  EDUCATION/QUALIFICATIONS
 
 
 
  You must be currently pursuing an undergraduate degree (started in the academic year of 2023) in any of the life or health sciences.
  Experience delivering multiple projects in an academic or professional setting.
  Demonstrated ability to plan, multi-task and prioritize
  Ability to work to deadlines
  Ability to collaborate with various stakeholders in a fast-paced environment, where priorities can change rapidly and you have to adapt on the spot.
  Demonstrated computer skills – requires excellent MS Office experience (specifically Excel, Word, Outlook)
  Demonstrated teamwork, communication (written and verbal), and organizational skills
 
 
 
  Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. Join our exceptional team and embrace a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact. For more information about Fortrea, visit www.fortrea.com.
 
 
 
  Fortrea is proud to be an Equal Opportunity Employer:
 
 
   As an EOE/AA employer, Fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.
 
 
 
  For more information about how we collect and store your personal data, please see our 
  
   Privacy Statement
  .
 


Clinical Research Technician, 2025 12-month Internship, Leeds - Fortrea

Clinical Research Technician, 2025 12-month Internship, Leeds

You should be pursuing a relevant undergraduate degree, have project experience, strong communication skills, attention to detail, and thrive in a fast-paced, collaborative environment.

You will manage clinical data, ensure accuracy, collaborate globally, and contribute to medical studies, gaining hands-on experience from day one.

<div>
 <div>
  As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff conducting operations in more than 90 countries, Fortrea is transforming drug and device development for partners and patients across the globe.
 </div>
 <div></div>
 <div>
  Launch your global career with Fortrea’s 2025 12-month Internship Program. We are seeking Clinical Data Management and Statistical Programming Interns to be office-based in Leeds, UK, starting July 1st 2025.
 </div>
 <div></div>
 <div>
  <br> As a Fortrea intern, from your first day, you will complement your education in STEM+ fields working on real department assignments, always linked to our mission to deliver solutions that bring life-changing medicines to patients faster.
 </div>
 <div></div>
 <div>
  <br> We will support your development and career exploration through:
 </div>
 <div></div>
 <ul>
  <li>Dedicated mentors</li>
  <li>Program workshops</li>
  <li>Leadership speakers</li>
  <li>Employee Resource Groups</li>
  <li>Panel discussions</li>
  <li>Small group ‘coffee chats’</li>
 </ul>
 <div></div>
 <div>
  <br> Capitalise on a dedicated training and development program that will support your career aspirations and take pride in delivering work that helps save the lives of millions of people around the world.
 </div>
 <div></div>
 <div>
  About the Team
 </div>
 <div></div>
 <ul>
  <li>Fortrea is a global contract research organization with offices and sites all over the globe involved with studies ranging across all aspects of clinical trials – this opportunity in particular is for our Early Phase Clinical Data Management and Statistical Programming groups who work with multiple therapeutic areas like Cardiovascular, Respiratory Disorders, Central Nervous System and Infectious Diseases, Oncology to name a few.</li>
 </ul>
 <div></div>
 <div>
  <br> Internship Opportunity Summary
 </div>
 <div></div>
 <ul>
  <li>Learn from Day One: Embrace a hands-on learning experience from the moment you step in the door. At Fortrea we believe in nurturing talent. You won't just be a part of our team; you'll be a vital contributor from your first day, gaining practical insights and real-world skills.</li>
 </ul>
 <div></div>
 <ul>
  <li>Global Exposure: Immerse yourself in the world of international clinical research. Collaborate with professionals from diverse cultures and backgrounds, broadening your horizons and enhancing your global perspective.</li>
 </ul>
 <div></div>
 <ul>
  <li>Own Your Responsibilities: Take charge of clinical data management processes and witness the impact of your work on pioneering medical studies. You won't be fetching coffee here; you'll be at the forefront of managing critical data, ensuring its accuracy, and supporting the development of life-changing treatments.</li>
 </ul>
 <div></div>
 <div>
  Your profile
 </div>
 <div></div>
 <ul>
  <li><br> Currently pursuing an undergraduate degree, preferably in life science, health science, or related subjects</li>
  <li>Experience delivering multiple projects in an academic or professional setting.</li>
  <li>Ability to collaborate and communicate with your team and wider colleagues.</li>
  <li>Embraces diverse ways of thinking through various forms collaboration and partnership.</li>
  <li>Exceptional attention to detail and organizational abilities.</li>
  <li>Eagerness to learn and adapt in a fast-paced environment.</li>
  <li>Excellent communication and teamwork skills.</li>
  <li>Fluent in English (both written and spoken), and excellent communication, interpersonal and organizational skills.</li>
 </ul>
 <div></div>
 <div>
  Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. Join our exceptional team and embrace a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact. For more information about Fortrea, visit www.fortrea.com.
 </div>
 <div></div>
 <div>
  Fortrea is proud to be an Equal Opportunity Employer:
 </div>
 <div>
  <br> As an EOE/AA employer, Fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.
 </div>
 <div></div>
 <div>
  For more information about how we collect and store your personal data, please see our 
  <div>
   Privacy Statement
  </div>.
 </div>
</div>


 
  As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff conducting operations in more than 90 countries, Fortrea is transforming drug and device development for partners and patients across the globe.
 
 
 
  Launch your global career with Fortrea’s 2025 12-month Internship Program. We are seeking Clinical Data Management and Statistical Programming Interns to be office-based in Leeds, UK, starting July 1st 2025.
 
 
 
   As a Fortrea intern, from your first day, you will complement your education in STEM+ fields working on real department assignments, always linked to our mission to deliver solutions that bring life-changing medicines to patients faster.
 
 
 
   We will support your development and career exploration through:
 
 
 
  Dedicated mentors
  Program workshops
  Leadership speakers
  Employee Resource Groups
  Panel discussions
  Small group ‘coffee chats’
 
 
 
   Capitalise on a dedicated training and development program that will support your career aspirations and take pride in delivering work that helps save the lives of millions of people around the world.
 
 
 
  About the Team
 
 
 
  Fortrea is a global contract research organization with offices and sites all over the globe involved with studies ranging across all aspects of clinical trials – this opportunity in particular is for our Early Phase Clinical Data Management and Statistical Programming groups who work with multiple therapeutic areas like Cardiovascular, Respiratory Disorders, Central Nervous System and Infectious Diseases, Oncology to name a few.
 
 
 
   Internship Opportunity Summary
 
 
 
  Learn from Day One: Embrace a hands-on learning experience from the moment you step in the door. At Fortrea we believe in nurturing talent. You won't just be a part of our team; you'll be a vital contributor from your first day, gaining practical insights and real-world skills.
 
 
 
  Global Exposure: Immerse yourself in the world of international clinical research. Collaborate with professionals from diverse cultures and backgrounds, broadening your horizons and enhancing your global perspective.
 
 
 
  Own Your Responsibilities: Take charge of clinical data management processes and witness the impact of your work on pioneering medical studies. You won't be fetching coffee here; you'll be at the forefront of managing critical data, ensuring its accuracy, and supporting the development of life-changing treatments.
 
 
 
  Your profile
 
 
 
   Currently pursuing an undergraduate degree, preferably in life science, health science, or related subjects
  Experience delivering multiple projects in an academic or professional setting.
  Ability to collaborate and communicate with your team and wider colleagues.
  Embraces diverse ways of thinking through various forms collaboration and partnership.
  Exceptional attention to detail and organizational abilities.
  Eagerness to learn and adapt in a fast-paced environment.
  Excellent communication and teamwork skills.
  Fluent in English (both written and spoken), and excellent communication, interpersonal and organizational skills.
 
 
 
  Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. Join our exceptional team and embrace a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact. For more information about Fortrea, visit www.fortrea.com.
 
 
 
  Fortrea is proud to be an Equal Opportunity Employer:
 
 
   As an EOE/AA employer, Fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.
 
 
 
  For more information about how we collect and store your personal data, please see our 
  
   Privacy Statement
  .
 


12-Month Internship – Clinical Data Management or Statistical Programming – Leeds, UK - Fortrea

12-Month Internship – Clinical Data Management or Statistical Programming – Leeds, UK

You must manage adverse event reports, ensure data accuracy, write narratives, support reporting, mentor staff, and understand safety protocols and regulations in pharmacovigilance.

You will manage adverse event reports, ensure accurate data processing, assist with regulatory submissions, support safety database maintenance, and mentor junior staff in case handling.

Data

Pune

<div>
 <div>
  As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff conducting operations in more than 90 countries, Fortrea is transforming drug and device development for partners and patients across the globe.
 </div>
 <div></div>
 <div>
  Manage the receipt and processing of all adverse event reports reported either spontaneously from any source or from a clinical trial. This includes, but is not limited to:<br>
  <ul></ul> Data entry of safety data onto adverse event database(s) and tracking systems.<br>
  <ul></ul> Review of adverse events for completeness, accuracy and appropriateness for expedited reporting.<br>
  <ul></ul> Write patient narratives and code adverse events accurately using MedDRA.<br>
  <ul></ul> Determine listedness against appropriate label (for Marketed products, if applicable).<br>
  <ul></ul> Identifies clinically significant information missing from the reports and ensures its collection and follow-up.<br> <br>
  <ul>
   <li>Ensure all cases that require expediting reporting to worldwide Regulatory Agencies</li>
  </ul> and other required parties are processed swiftly and appropriately within required<br> timelines.<br>
  <ul>
   <li>Reporting of endpoints to clients, Regulatory Authorities, Ethics Committees,</li>
  </ul> investigators, 3rd party vendors, Partners and Fortrea project personnel, if required,<br> within study specified timelines.<br>
  <ul>
   <li>Submission of expedited Serious Adverse Event (SAE) reports to clients, Regulatory</li>
  </ul> Authorities, Ethics Committees, investigators, 3rd party vendors, Partners and<br> Fortrea project personnel, if required &amp; as agreed with client during study set-up,<br> within study specified timelines.<br>
  <ul>
   <li>Perform Database reconciliation with Data Management team or sponsor/client as needed.</li>
   <li>Perform processing and/or review and submission of Expedited Safety Reports (ESRs), Periodic</li>
  </ul> Safety Reports (PSRs), including but not limited to:<br>
  <ul>
   <li>Maintenance of adverse event tracking systems</li>
   <li>Set-up and maintenance of project files and central files for documentation</li>
   <li>Assist with the reporting of ESRs &amp; PSRs to clients, Regulatory Authorities, Ethics</li>
  </ul> Committees, investigators and Fortrea project personnel, as required, within study<br> specified timelines.<br>
  <ul>
   <li>Maintain a strong understanding of Fortrea’s safety database conventions or client specific</li>
  </ul> database conventions, as appropriate.<br>
  <ul>
   <li>Perform quality review or peer review of processed reports and support the Line</li>
  </ul> Management with trends and actions needed.<br>
  <ul>
   <li>Begin participating in signal detection and trend &amp; pattern recognition activities, as</li>
  </ul> appropriate.<br>
  <ul>
   <li>Assist in the preparation of listings for Annual IND reports, Periodic Reports (PRs) like</li>
  </ul> Periodic Safety Update Reports (PSURs), Development Safety Update Reports (DSURs) etc.<br>
  <ul>
   <li>Begin participating in the generation of monthly status and other project-specific reports</li>
  </ul> ensuring the quality and accuracy of metrics and data provided.<br>
  <ul>
   <li>Support/train/mentor less experienced safety staff in all aspects of case-handling, adverse</li>
  </ul> event reporting<br>
  <ul>
   <li>Maintain a comprehensive understanding of Standard Operating Procedures (SOPs), Work</li>
  </ul> Instructions (WI), guidance documents and directives associated with safety management,<br> reporting and pharmacovigilance.<br>
  <ul>
   <li>Assist with review and update of Safety Management Plans (SMPs), Reconciliation Plans,</li>
  </ul> and other safety- specific plans ensuring optimal efficiency.<br>
  <ul>
   <li>Participate in Fortrea project team and client meetings, as appropriate.</li>
   <li>Prepare and support coordination of safety study files for archiving at completion of</li>
  </ul> projects.<br>
  <ul>
   <li>Contribute to root cause analysis, including the CAPA plan development &amp; implementation.</li>
   <li>Support Audits and/or inspections preparation</li>
   <li>Assist in review of cumulative safety data for submission to Drug Safety Monitoring Boards</li>
  </ul> (DSMBs), regulatory authorities or clients, if applicable and coordination of end point<br> committees.<br>
  <ul>
   <li>All other duties as needed or assigned.</li>
  </ul>
 </div>
 <div>
  <br> Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. Join our exceptional team and embrace a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact. For more information about Fortrea, visit www.fortrea.com.
 </div>
 <div></div>
 <div>
  Fortrea is proud to be an Equal Opportunity Employer:
 </div>
 <div>
  <br> As an EOE/AA employer, Fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.
 </div>
 <div></div>
 <div>
  For more information about how we collect and store your personal data, please see our 
  <div>
   Privacy Statement
  </div>.
 </div>
</div>


 
  As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff conducting operations in more than 90 countries, Fortrea is transforming drug and device development for partners and patients across the globe.
 
 
 
  Manage the receipt and processing of all adverse event reports reported either spontaneously from any source or from a clinical trial. This includes, but is not limited to:
   Data entry of safety data onto adverse event database(s) and tracking systems.
   Review of adverse events for completeness, accuracy and appropriateness for expedited reporting.
   Write patient narratives and code adverse events accurately using MedDRA.
   Determine listedness against appropriate label (for Marketed products, if applicable).
   Identifies clinically significant information missing from the reports and ensures its collection and follow-up. 
  
   Ensure all cases that require expediting reporting to worldwide Regulatory Agencies
   and other required parties are processed swiftly and appropriately within required timelines.
  
   Reporting of endpoints to clients, Regulatory Authorities, Ethics Committees,
   investigators, 3rd party vendors, Partners and Fortrea project personnel, if required, within study specified timelines.
  
   Submission of expedited Serious Adverse Event (SAE) reports to clients, Regulatory
   Authorities, Ethics Committees, investigators, 3rd party vendors, Partners and Fortrea project personnel, if required & as agreed with client during study set-up, within study specified timelines.
  
   Perform Database reconciliation with Data Management team or sponsor/client as needed.
   Perform processing and/or review and submission of Expedited Safety Reports (ESRs), Periodic
   Safety Reports (PSRs), including but not limited to:
  
   Maintenance of adverse event tracking systems
   Set-up and maintenance of project files and central files for documentation
   Assist with the reporting of ESRs & PSRs to clients, Regulatory Authorities, Ethics
   Committees, investigators and Fortrea project personnel, as required, within study specified timelines.
  
   Maintain a strong understanding of Fortrea’s safety database conventions or client specific
   database conventions, as appropriate.
  
   Perform quality review or peer review of processed reports and support the Line
   Management with trends and actions needed.
  
   Begin participating in signal detection and trend & pattern recognition activities, as
   appropriate.
  
   Assist in the preparation of listings for Annual IND reports, Periodic Reports (PRs) like
   Periodic Safety Update Reports (PSURs), Development Safety Update Reports (DSURs) etc.
  
   Begin participating in the generation of monthly status and other project-specific reports
   ensuring the quality and accuracy of metrics and data provided.
  
   Support/train/mentor less experienced safety staff in all aspects of case-handling, adverse
   event reporting
  
   Maintain a comprehensive understanding of Standard Operating Procedures (SOPs), Work
   Instructions (WI), guidance documents and directives associated with safety management, reporting and pharmacovigilance.
  
   Assist with review and update of Safety Management Plans (SMPs), Reconciliation Plans,
   and other safety- specific plans ensuring optimal efficiency.
  
   Participate in Fortrea project team and client meetings, as appropriate.
   Prepare and support coordination of safety study files for archiving at completion of
   projects.
  
   Contribute to root cause analysis, including the CAPA plan development & implementation.
   Support Audits and/or inspections preparation
   Assist in review of cumulative safety data for submission to Drug Safety Monitoring Boards
   (DSMBs), regulatory authorities or clients, if applicable and coordination of end point committees.
  
   All other duties as needed or assigned.
  
 
 
   Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. Join our exceptional team and embrace a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact. For more information about Fortrea, visit www.fortrea.com.
 
 
 
  Fortrea is proud to be an Equal Opportunity Employer:
 
 
   As an EOE/AA employer, Fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.
 
 
 
  For more information about how we collect and store your personal data, please see our 
  
   Privacy Statement
  .
 


Fortrea

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