Project Specialist - Clinical Registry Coordinator - UK Based
- 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.
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Originally posted on Himalayas
Quality
- x Salary range stated weight 35%
- + Remote policy stated weight 20%
- + Location stated weight 15%
- + Organisation stated weight 15%
- + Publication date stated weight 15%
Not enough history yet to judge honesty signals.
Timeline
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#243785 2026-08-21 13:39 UTCPublished