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IQVIA

Clinical Trials Assistant

Reading
Posted about 22 hours ago
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Join IQVIA on our mission to accelerate innovation for a healthier world!

We are seeking a Clinical Trials Assistant to join our cFSP (sponsor-dedicated) team.

This position requires candidates able to commit to ad-hoc travel to sponsor's office in Maidenhead, Berkshire.

Why IQVIA?

  • We share a passion for the work we do, and the impact it has on customers and patients
  • We are innovative, curious, and feel empowered to explore new ideas and ways of working
  • We collaborate to bring out the best in each other and get the most out of our different skills, perspectives, and expertise
  • We are committed to growth, always learning, and making the most of agile career opportunities
  • 2026 "Glassdoor Best Place to Work in the UK"
  • Recognised as #1 in its category on the 2026 Fortune® World’s Most Admired Companies™ list (for the FIFTH consecutive year!)

Key Responsibilities

  • Maintain and update clinical systems and documentation, including the Trial Master File.
  • Support the preparation, distribution, filing, and archiving of clinical documents and reports.
  • Conduct periodic reviews of study files to ensure completeness and compliance.
  • Assist with clinical trial supply logistics and tracking.
  • Manage Case Report Forms (CRFs), queries, and clinical data flow.
  • Serve as a central point of contact for project communications and documentation.

Reasons to use Rodeo

I’m in my final year doing Economics and I don’t know whether to apply for grad schemes now or do a masters first. What do you think?

Honest answer — it depends on where you want to end up. A lot of top grad schemes (Big 4, civil service, banking) don’t need a masters. Let’s look at the ones you’d be competitive for now, and we can decide if a masters actually adds anything.

Also worth knowing: most autumn 2026 applications are open now. Timing matters more than you think.

Start with a chat, not a search bar

Grad scheme, placement, apprenticeship? Not sure what you want yet — that's fine. Your agent talks it through with you and turns "I have no idea" into a shortlist.

P

Graduate Consultant — 2026 Scheme

PwC·London, UK
£35,000/yr

Why you're a good match

Strong

Your economics background and your summer at a regional bank line up with what PwC looks for on the consulting scheme. Applications close in four weeks.

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Why you're a good match

You’ve got the grades and the economics background, and your bank internship is exactly the experience this scheme looks for. Apply soon — deadlines close within the month.

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Strong

Experience fit

Your summer at the bank plus your econometrics coursework map directly to the day-one responsibilities on this scheme — client modelling, market briefings, and deal support.

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Only hits

No noise. No "maybe this fits." Just roles with a clear explanation of why they're right — and where to focus when applying.

What We’re Looking For

  • Previous clinical trials support experience required.
  • Knowledge of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH).
  • Degree in life sciences or equivalent industry experience.
  • Proficiency in Microsoft Word, Excel, and PowerPoint.
  • Strong written and verbal communication skills in English.
  • Excellent time management, organization, and collaboration skills.

Please note: This role is not eligible for UK visa sponsorship.

Apply today and forge a career with greater purpose, make an impact, and never stop learning!

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IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

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Skills

Clinical Trial Support
Trial Master File Management
Good Clinical Practice (GCP)
ICH Guidelines
Clinical Data Flow
Case Report Forms (CRFs)
Microsoft Word
Microsoft Excel
Microsoft PowerPoint
Time Management
Organization
Collaboration
Written Communication
Verbal Communication

Location

Reading, England, United Kingdom

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