Clinical Data Associate II
On-site · Bengaluru, Karnataka, India or Chennai, Tamil Nadu, India
Job Summary
Clinical Data Associate II provides data management support across the clinical trial lifecycle under supervision. Responsibilities include supporting the Lead DM as a back-up, data entry for paper-CRF studies, quality control of data entry, developing CRF specifications from study protocols, building clinical databases, conducting database build UAT, maintaining data management documentation, specifying requirements for edit checks, training CRF/EDC personnel, reviewing and querying trial data per the Data Management Plan, running line listings and status metrics, medical coding to ensure logical consistency, SAE/AE reconciliation, liaising with external vendors in a project-management capacity, and potential SAS programming support; some travel may be required. Qualifications include a Bachelor's degree (or related experience) and 2-4 years of experience; proficiency in Microsoft Office; strong organizational and communication skills; and preferred experience in a clinical/healthcare discipline. Precision Medicine Group is an equal opportunity employer; privacy notices apply. Location hints indicate Bengaluru and Chennai, India.
Required Qualifications
- Bachelor's degree or equivalent experience
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