iqvia
Clinical Data Manager - FSP (Homebased - UK)
At a Glance
- Location
- Reading, Berkshire, United Kingdom
- Employment
- Full time
- Experience
- 5+ years
- Posted
- 2026-08-14
Key Requirements
Required Skills
Domain Knowledge
- Pharmaceutical
Requirements
Minimum of 5 years of data management experience
Oracle Inform EDC experience
Oncology and/or inflammatory therapeutic area experience is preferred.
CRO or Pharma data management experience
Responsibilities
Responsible for communicating key clinical data management metrics (e.g., data entry status, query resolution and aging, etc.) and determining appropriate actions in conjunction with study team.
Responsible for the review, development and/or writing of clinical trial documents and manuals, including but not limited to Case Report Forms, Edit Checks, Data Management Plans, Clinical Data Review Plans and eCRF Completion Guidelines.
Participate in User Acceptance Testing (UAT), as needed.
Participate in Quality Control (QC), as needed.
Responsible for working with the assigned Clinical Database Programmer(s) to ensure the development of the Data Flow Chart(s), Data Transfer Specifications and Import Guidelines.
Assist with site and/or third party vendor training on CDM-related topics.