FSP CRA ─ with Sign-on Bonus
Core
Ensure clinical studies at investigator sites comply with protocols, ICH GCP, and local laws to protect subject rights and ensure data accuracy.
Role type
Senior Clinical Research Associate (Level II)
Builds
Clinical monitoring activities for pharmaceutical and biotech clients
Domain
Clinical research / Pharmaceuticals
Deliverable
physical/clinical work
Required skills
Independent on-site monitoring, ICH-GCP compliance, MFDS and FDA requirements, medical/therapeutic area knowledge, medical terminology
Preferred skills
None stated
Technologies
None stated
Responsibilities
Perform and coordinate all aspects of the clinical monitoring process; conduct monitoring activities independently; ensure compliance with approved protocols and regulatory requirements.
Seniority
Senior, hands-on IC
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