Clinical Data Manager
Location: Europe
Contract Type: One Year Contract
Working Pattern: Full Time
The Opportunity
We are currently seeking an experienced Clinical Data Manager to take ownership of end-to-end data management activities across clinical studies. This is an excellent opportunity for a data management professional with strong experience in clinical databases, EDC systems, data cleaning and study documentation to take a leading role within a fast-paced clinical research environment.
You will work closely with project teams, sponsors and other stakeholders to ensure high-quality, accurate and timely clinical data throughout the lifecycle of a study.
Key Responsibilities
- Independently lead end-to-end clinical data management activities, including database design, database setup, CRF and non-CRF collection tools, data cleaning and documentation.
- Develop and maintain Data Management Plans (DMPs), Data Validation Plans, completion guidelines, data management reports and other study documentation.
- Coordinate study team reviews of CRFs, identifying potential data collection, database structure and data entry issues.
- Ensure captured data complies with the clinical protocol and data management plan.
- Lead the development of data validation plans and coordinate user acceptance testing (UAT) of CRFs and associated edit checks.
- Manage data cleaning activities, including the generation, tracking and resolution of queries and discrepancies.
- Ensure accurate and timely reconciliation of third-party data with Clinical Data Management System (CDMS) data.
- Track CRFs as they progress through the Data Management function.
- Work closely with the Project Manager throughout the study lifecycle to provide updates and resolve issues.
- Liaise directly with sponsors when required, providing data management updates and discussing study-related issues.
- Ensure the Trial Master File (TMF) remains accurate, complete and up to date throughout the trial.
- Mentor and train Data Managers, supporting the development of team capabilities.
- Undertake additional responsibilities as required.
About You
The ideal candidate will have:
- A Bachelor’s degree or international equivalent, preferably in a technical, clinical or health-related discipline, or an equivalent combination of education, training and experience.
- 3–5 years of practical experience leading database management activities within clinical research.
- Hands-on experience with commercial Clinical Data Management Systems (CDMS) and/or EDC platforms, such as Oracle RDC/Inform, Medidata Rave, DataLabs or similar.
- Proven experience across the core responsibilities of clinical data management.
- Excellent written and verbal English communication skills.
- Strong IT skills, including proficiency with Microsoft Office, Outlook and Excel.
- A customer-focused approach, with a proven ability to deliver high-quality and timely work while taking ownership of tasks.
- Strong analytical, organisational and problem-solving skills.
- The ability to work independently, manage multiple projects and adapt effectively to changing priorities in a fast-paced environment.
Why Apply?
This is a great opportunity for an experienced Clinical Data Manager to take ownership of important study activities, work directly with cross-functional teams and sponsors, and contribute to the delivery of high-quality clinical research data.
