Data Manager for Clinical Trials

About the role

The Clinical Data Manager plays a critical role in ensuring high‑quality data handling for clinical research projects. You will work with large volumes of clinical or medical data, supporting the delivery of accurate and timely trial results.

Key responsibilities

• Set up, test, maintain, and enter data into clinical databases (eCRF, EDC).
• Design eCRF, Data Management Plans, and Validation Plans; test EDC systems.
• Perform data entry, follow‑up, validation, manual CRF review and SAE reconciliation.
• Code medical data, track metrics, and prepare databases for lock.
• Coordinate processing, dispatch, and archiving of CRFs/queries; conduct QC checks and support audits.
• Train site staff and project teams on CRF completion and data management topics.

Required profile

• University degree in Life Sciences (Pharmacy degree is a plus).
• Proven experience managing clinical or medical data.
• Full professional proficiency in English.
• Strong organisational and time‑management abilities; capable of independent multi‑tasking.

Required skills

• Experience with Clinical Data Management systems such as Medidata Rave or Oracle InForm.
• Proficiency in Microsoft Office applications.