FSP_Clinical Research Associate (Sponsor: Biogen) ─ with Sign-on Bonus
Core
Ensures clinical studies at investigator sites comply with protocols, ICH GCP, and local laws to protect subject rights and ensure data accuracy.
Role type
Clinical Research Associate (CRA)
Builds
Clinical trial data integrity and regulatory compliance
Domain
Pharmaceutical / Clinical Research
Required skills
ICH-GCP knowledge, MFDS and FDA requirements, medical/therapeutic area knowledge, medical terminology, independent on-site monitoring, communication, collaboration, time management
Preferred skills
University degree in nursing or life-sciences, 3+ years independent on-site monitoring experience in Pharma or CRO
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
Mid-level, hands-on IC