Experienced CRA
Core
Senior Clinical Research Associate conducting risk-based monitoring of clinical trial sites across Sweden, Norway, and Finland to ensure protocol compliance and data reliability.
Role type
Senior Clinical Research Associate (CRA)
Builds
Clinical trial data integrity and regulatory compliance for life sciences sponsors
Domain
Clinical Research / Life Sciences / Neuroscience
Deliverable
client delivery
Required skills
Risk-based monitoring, root cause analysis, ICH-GCP compliance, clinical trial site initiation and close-out, data review (SDR/SDV/CRF), investigator payment management, medical terminology knowledge, Microsoft Office proficiency
Preferred skills
Neuroscience experience, experience across all study phases, ability to monitor in multiple countries (Sweden, Norway, Finland)
Technologies
Clinical Trial Management Systems
Responsibilities
Monitor investigator sites using risk-based approaches; ensure data accuracy through document and data review; initiate and close out clinical trial sites; manage investigator payments and meetings; conduct on-site file reviews; provide trial status tracking reports.
Seniority
Senior, hands-on IC
