Project Specialist - Clinical Registry Coordinator - UK Based

Lifelancer - United States - original posting ->
Status
Open
Remote policy
Remote
Employment type
Not stated
Salary
Not stated
Categories
Clinical-Registry-Coordinator, Clinical-Research, Clinical-Development, Project-Specialist, Healthcare-Research, Clinical-Project-Specialist, Clinical-Project-Coordinator, Clinical-Registry-Specialist, Clinical-Project-Associate
Source
himalayas
First observed
2026-08-21 13:39 UTC
Last seen
2026-08-21 13:39 UTC
Source claims posted
2026-08-21 13:34 UTC
Consecutive misses
0 of 10

What the posting says

Job Title: Project Specialist - Clinical Registry Coordinator - UK Based

Job Location: Reading, Berkshire, United Kingdom

Job Location Type: Remote

Job Contract Type: Full-time

Job Seniority Level:

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.

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

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.

This job is curated by Lifelancer.

Lifelancer is a talent-hiring platform in Life Sciences, Pharma and IT. The platform connects talent with opportunities in pharma, biotech, health sciences, healthtech and IT domains.

Please apply via Lifelancer platform to get connected to the application page and to find similar roles.

Originally posted on Himalayas

Quality

Completeness: 65%

Not enough history yet to judge honesty signals.

Timeline

  1. *
    #243785 2026-08-21 13:39 UTC
    Published