Clinical Research Associate - FSP - Sweden
Core
Monitor clinical trial investigator sites to ensure compliance with protocols and regulations, ensuring data accuracy and patient safety.
Role type
Clinical Research Associate (CRA)
Builds
Clinical trial data integrity and regulatory compliance for life science therapies
Domain
Clinical Research / Life Sciences / Pharma & Biotech
Deliverable
client delivery
Required skills
Risk-based monitoring, root cause analysis, data verification (SDR/SDV), ICH-GCP knowledge, site initiation and close-out, regulatory compliance
Preferred skills
Cell & Gene Therapy study experience, medical/therapeutic area knowledge, trial status tracking
Technologies
Clinical Trial Management Systems, Microsoft Office
Responsibilities
Monitor investigator sites using risk-based approaches; ensure data accuracy through document and source data review; initiate and close out clinical trial sites; conduct on-site file reviews; track trial status and progress; participate in investigator meetings and payment processes.
Seniority
Individual Contributor