CRA-fully client dedicated- Finland
Core
Clinical Research Associate monitoring investigator sites to ensure protocol compliance and data accuracy for life science clinical trials.
Role type
Clinical Research Associate (CRA)
Builds
Clinical trial data integrity and regulatory compliance
Domain
Life Sciences / Clinical Research
Deliverable
client delivery
Required skills
Risk-based monitoring, root cause analysis, data verification (SDR/SDV), ICH-GCP knowledge, site initiation and close-out, investigator payment processing, trial status reporting
Preferred skills
Neuroscience experience, all study phases experience (start to close-out), Microsoft Office proficiency
Technologies
Clinical Trial Management Systems
Responsibilities
Monitor investigator sites using risk-based approaches; ensure data accuracy through document and source data review; assess investigational product inventory; initiate and close out clinical trial sites; conduct on-site file reviews; provide trial status reports to management.
Seniority
Individual Contributor
