Data Manager for Clinical Trials
HybridTallinn, Harjumaa, Estonia
Job Summary
Track database set-up, testing, maintenance, and data entry while designing eCRFs, Data Management, and Data Validation Plans. Review study documents to develop project-specific guidelines and instructions, ensuring data entry, follow-up, and validation including manual CRF review and SAE reconciliation. Code medical data, perform database QC checks, and prepare for audits. Coordinate CRF processing, dispatch, and archiving, and maintain working files. Train site staff on CRF completion and data management topics. Lead metrics tracking to database lock. Requires a College/University degree in Life Science or Pharmacy, proficiency in Clinical Data Management systems like Medidata Rave or Oracle InForm, and full working proficiency in English.
Required Qualifications
- College/University degree
- Life Science degree
- Pharmacy degree
- Demonstrated experience of managing clinical or medical data
- Full working proficiency in English
- Experience with Clinical Data Management systems (e.g. Medidata Rave, Oracle InForm)
- Proficiency in MS Office applications
- Organisational and time management skills
- Ability to work independently and multi-task
Desired Qualifications
- Life Science degree
- Pharmacy degree
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