Senior Clinical Research Associate I Sponsor-Dedicated FSP - Germany (m/f/d)
Core
Senior Clinical Research Associate conducting risk-based monitoring, site management, and compliance assurance for clinical trials across pharmaceutical and biotech sectors.
Role type
Senior IC clinical research associate (monitoring & site management)
Builds
Clinical trial execution ensuring protocol adherence, data reliability, and regulatory compliance for sponsors
Domain
Life Sciences / Clinical Research / Pharmaceutical Trials
Deliverable
client delivery
Required skills
Risk-based monitoring, root cause analysis, protocol compliance, ICH-GCP guidelines, site initiation, data review (SDR/SDV/CRF), investigator management, audit readiness
Preferred skills
Medical/therapeutic area knowledge, problem-solving, travel adaptability
Technologies
Clinical Trial Management Systems (CTMS), Microsoft Office
Responsibilities
Monitor investigator sites using risk-based approach; initiate and manage clinical trial sites; ensure audit readiness and document compliance; track trial status and generate progress reports; facilitate communication between sites, clients, and project teams; conduct on-site file reviews and inventory checks.
Seniority
Senior, hands-on IC