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About the Role:
- Provide data management support and assistance in all aspects of clinical trial data management from study start-up to post database lock.
- Support the Lead Data Manager as a back-up or team member, ensuring continuity and timely task completion.
Key Responsibilities:
- Develop CRF specifications from the clinical study protocol and coordinate review and feedback from stakeholders.
- Build clinical databases, conduct UAT, and maintain quality-controlled documentation.
- Review and query clinical trial data, perform medical coding, and assist with SAE/AE reconciliation.
What We’re Looking For:
- Bachelor’s degree and around 2 years of experience as a Clinical Data Associate in a CRO/Pharma/Biotech.
- Proficiency in Microsoft Office and excellent organizational and communication skills.
- Professional use of English; ability to handle a variety of clinical research tasks.
Precision for Medicine
Precision for Medicine is a global precision medicine clinical research services organization that improves clinical research and development for new therapeutics. They integrate clinical operations, laboratory expertise, and data sciences, with a focus on oncology and rare disease.