Senior Clinical Research Associate (CRA) - Remote in Sao Paulo
Core
Conduct on-site monitoring visits for clinical trials to ensure data integrity, protocol compliance, and patient safety across drug and medical device development.
Role type
Senior Clinical Research Associate (CRA)
Builds
Clinical trial data and regulatory compliance for pharmaceutical and medical device companies
Domain
Clinical Research / Life Sciences
Deliverable
client delivery
Required skills
Clinical monitoring, protocol adherence, source data verification, adverse event reporting, regulatory document review, patient recruitment assessment, site qualification, investigational product accountability
Preferred skills
CRC experience, therapeutic area expertise, mentoring
Technologies
None stated
Responsibilities
Conduct qualification, initiation, monitoring, and closeout visits; Verify investigator qualifications and resources; Review medical records and source documentation against CRFs; Monitor adverse events and serious adverse events; Assess patient recruitment and retention; Complete monitoring reports and follow-up letters
Seniority
Senior, hands-on IC