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IQVIA

Clinical Registry Coordinator - UK Based

Reading
Posted 1 day ago
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Essential Functions

  • Provides clinical registry support, oversight, and/or accountability for one or more development programs for clinical trials.
  • Takes a leadership role with the clinical development team and other internal and external partners to establish, align, and confirm clinical registry expectations for assigned trial(s).
  • Responsible for submission of approved documents and content to registries worldwide. Submissions are made by the Clinical Registry Administrators.
  • Responsible for tracking, reporting, and documentation of disclosure records and associated documents in tools and systems used by the clinical registry group.
  • Assists business partners, external partners, and local operating companies in maintaining accurate and correct (source) data relevant to the disclosure process.
  • Ensures timely resolution of planning issues to ensure compliant delivery of the disclosure planning.
  • Ensures deliverables are on time.

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.

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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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Qualifications

  • A minimum of 4 years of relevant pharmaceutical/scientific experience in a clinical development environment (pharmaceutical, medical device, CRO, or other clinical development service organization) is required.
  • Bachelor’s degree in Health or Science discipline is required with experience in clinical research.
  • Clinical Registry experience preferred.
  • Experience working on a clinical trial or regulatory document management preferred.

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

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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 Registry Support
Clinical Trial Oversight
Clinical Development
Regulatory Document Management
Data Tracking
Disclosure Planning
Clinical Research
Pharmaceutical Industry Knowledge
Reporting
Documentation
Stakeholder Management

Location

Reading, England, United Kingdom

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