Data Coordinator

Job Summary

Working remotely on a part-time basis, the PRN Data Coordinator will ensure the accurate transcription of source data into Case Report Forms (CRFs) during clinical trials while adhering to Good Clinical Practice guidelines under the supervision of the Senior Manager, Study Conduct.

Key responsibilities

• Review study protocols for assigned studies
• Ensure accurate reflection of source documents on the Case Report Form
• Assist with the reconciliation of study records for archiving

Required qualifications

• Bachelor's degree or associate degree in Life Sciences or Health, or relevant experience in a phase I clinical environment
• Some knowledge of the clinical research process, including Good Clinical Practices
• Experience or coursework in the health field is preferred