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Job Description
Precision Medicine Group is seeking a Clinical Data Associate II to provide data management support for clinical trials. The Clinical Data Associate II will assist in all aspects of the data management process, from study start-up to post-database lock, under direct supervision. This role involves following SOPs/WIs, regulatory directives, and study-specific guidelines.Role involves:
  • Supporting the Lead DM as a back-up and/or team member.
  • Performing data entry for paper-CRF studies, as needed.
  • Developing CRF specifications from the clinical study protocol.
  • Assisting in building clinical databases and conducting UAT.
  • Creating and maintaining data management documentation.
  • Reviewing and querying clinical trial data.
  • Performing medical coding of medical terms.
  • Assisting with coordinating SAE/AE reconciliation.
  • Communicating with study sponsors, vendors, and project teams.
Requirements:
  • Bachelor's degree and/or related experience.
  • 2+ years of experience.
  • Proficiency in Microsoft Office.
  • Excellent organizational and communication skills.
  • Professional use of the English language.
Role offers:
  • Opportunity to work with a leading precision medicine company.
  • Chance to contribute to clinical research.
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