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.