Data Manager for Clinical Trials

About the role

PSI, a leading Contract Research Organization, is seeking a detail‑oriented Clinical Data Manager to support its global clinical trial programs. You will be responsible for ensuring high‑quality data capture, validation, and reporting across multiple studies.

Key responsibilities

• Set up, test, maintain, and enter data into clinical databases.
• Design eCRFs, Data Management Plans, and Validation Plans; test EDC systems.
• Perform data entry, follow‑up, manual CRF review, SAE reconciliation, and medical coding.
• Conduct database QC checks, generate metrics, and support database lock.
• Communicate with clients, project teams, and vendors on data‑related matters.
• Train site staff and internal teams on CRF completion and data management processes.
• Coordinate processing, dispatch, and archiving of CRFs and queries.

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.
• Ability to work independently and multitask.

Required skills

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

What we offer

• Opportunity to work in a globally recognised CRO.
• Inclusive culture that values diversity and professional growth.