Corporate Compliance Associate II
Core
Supports compliance to the clinical trial process by ensuring accurate data capture in eCRFs and managing study documentation.
Role type
Associate clinical trial compliance specialist
Builds
Clinical trial study documentation and eCRF data integrity
Domain
Life Sciences / Clinical Research
Deliverable
dashboards & analysis
Required skills
eCRF management, ICF verification, protocol deviation reporting, regulatory guideline adherence (ICH/GCP), data entry accuracy
Preferred skills
Medical terminology, multi-tasking, attention to detail
Technologies
eCRF systems, MS Office
Responsibilities
Maintain ISF and study trackers, assist with data capturing activities, ensure accurate entry of data in eCRF from source notes, verify protocol visit windows, report deviations and quality incidents, assist with drafting compliance reports
Seniority
Associate, entry-level IC