FSP CRA (Sponsor: GSK) ─ with Sign-on Bonus
Core
Clinical Research Associate conducting risk-based monitoring, site management, and regulatory compliance for pharmaceutical clinical trials.
Role type
Clinical Research Associate (Level II)
Builds
Clinical trial data integrity and regulatory compliance for pharmaceutical sponsors
Domain
Life Sciences / Clinical Research
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
Clinical monitoring, Root cause analysis, Risk-based monitoring, ICH-GCP guidelines, Protocol adherence, Site initiation, Trial close-out, Data review (SDR/SDV/CRF), Investigational product inventory
Preferred skills
Medical/therapeutic area knowledge, Clinical Trial Management Systems, Microsoft Office
Technologies
Clinical Trial Management Systems, Microsoft Office
Responsibilities
Monitor investigator sites using risk-based approach; Ensure protocol and regulatory compliance; Manage site initiation and trial close-out; Conduct data reviews and document observations; Facilitate communication between sites, clients, and project teams; Respond to audits and inspections.
Seniority
Mid-level, hands-on IC