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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.

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