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Clinical Trial Assistant

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IQVIA

20d ago

  • Job
    Full-time
    Entry & Junior Level
  • Research & Development
    Healthcare
  • Reading

AI generated summary

  • You should have a life science degree or equivalent experience, 6-12 months in clinical trials, GCP/ICH knowledge, strong computer skills, and effective communication and organization abilities.
  • You will update clinical documents, assist with file reviews, manage trial supplies, track data flow, and coordinate project communications for the clinical team.

Requirements

  • Life science degree educated or equivalent industry experience.
  • Ideally 6-12 months clinical trials experience and / or knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
  • Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint.
  • Effective written and verbal communication skills including good command of English language.
  • Effective time management and organizational skills.
  • Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
  • Please note - this role is not eligible for UK visa sponsorship.

Responsibilities

  • Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems (e.g., Trial Master File (TMF)) that track site compliance and performance within project timelines.
  • Collaborate with clinical team on the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures.
  • Assist with periodic review of study files and completeness.
  • Collaborate with CRAs and RSU on the preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information.
  • Coordinate the tracking and management of Case Report Forms (CRFs), queries and clinical data flow.
  • Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation.

FAQs

What is the job title for this position?

The job title is Clinical Trial Assistant.

What company is offering this position?

The position is offered by IQVIA cFSP.

What is the main responsibility of the Clinical Trial Assistant?

The main responsibility is to perform daily administrative activities to ensure a complete and accurate Trial Master File delivery in collaboration with Clinical Research Associates and Regulatory and Start-Up teams.

Is this position fully remote?

No, while remote working is allowed, on-site work is required on an ad-hoc basis in Buckinghamshire.

What educational background is required for this position?

A life science degree or equivalent industry experience is required.

How much clinical trials experience is ideally needed for this role?

Ideally, 6-12 months of clinical trials experience is needed.

Are there specific guidelines that the candidate should be familiar with?

Yes, knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines is preferred.

What computer skills are necessary for the Clinical Trial Assistant position?

Proficiency in Microsoft Word, Excel, and PowerPoint is necessary.

What kind of communication skills are required for this role?

Effective written and verbal communication skills, along with a good command of the English language, are required.

Do we provide visa sponsorship for this role?

No, this role is not eligible for UK visa sponsorship.

What are the key organizational skills required for this position?

Effective time management and organizational skills are key requirements.

Who does the Clinical Trial Assistant collaborate with?

The Clinical Trial Assistant collaborates with Clinical Research Associates (CRAs) and Regulatory and Start-Up teams.

Is this position focused on patient interaction?

No, the role is primarily administrative and does not involve direct patient interaction.

How can I learn more about the company and its services?

You can learn more at the IQVIA careers website at https://jobs.iqvia.com.

Accelerate innovation for a healthier world.

Science & Healthcare
Industry
10,001+
Employees

Mission & Purpose

IQVIA (NYSE:IQV) is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. IQVIA creates intelligent connections across all aspects of healthcare through its analytics, transformative technology, big data resources and extensive domain expertise. IQVIA Connected Intelligence™ delivers powerful insights with speed and agility — enabling customers to accelerate the clinical development and commercialization of innovative medical treatments that improve healthcare outcomes for patients. With approximately 86,000 employees, IQVIA conducts operations in more than 100 countries. IQVIA is a global leader in protecting individual patient privacy. The company uses a wide variety of privacy-enhancing technologies and safeguards to protect individual privacy while generating and analyzing information on a scale that helps healthcare stakeholders identify disease patterns and correlate with the precise treatment path and therapy needed for better outcomes. IQVIA’s insights and execution capabilities help biotech, medical device and pharmaceutical companies, medical researchers, government agencies, payers and other healthcare stakeholders tap into a deeper understanding of diseases, human behaviors and scientific advances, in an effort to advance their path toward cures.

Benefits

  • Medical, dental and vision coverage

  • Employee Assistance Programs

  • Mental health support

  • Flexible work environment

  • Time off for leisure, personal time and corporate holidays

  • Parental leave for birth or adoption

  • Paid leave for other life matters (i.e., illness, bereavement, jury duty, military service, etc.)

  • Retirement and savings plans

  • Commuter benefits