Clinical Research Associate - All Levels
Core
Conduct clinical monitoring visits for drug and medical device development trials across Argentina to ensure protocol compliance and data accuracy.
Role type
Clinical Research Associate (CRA)
Builds
Clinical trial data and regulatory compliance for pharmaceutical and medical device companies
Domain
Clinical Research / Life Sciences
Deliverable
physical/clinical work
Required skills
Clinical monitoring, protocol adherence, source documentation verification, adverse event reporting, patient recruitment assessment, regulatory document review, investigational product accountability
Preferred skills
Clinical monitoring experience, clinical patient management, ISF preparation, TMF reconciliation
Technologies
GCP, SOPs, CRF, ISF, TMF
Responsibilities
Conduct qualification, initiation, monitoring, and closeout visits for research sites; Verify investigator qualifications and resources; Review medical records and source documentation against case report forms; Verify eligibility of enrolled subjects; Review adverse events and concomitant medications; Assess patient recruitment and retention success; Complete monitoring reports and follow-up letters.
Seniority
Entry-level to Mid-level (training provided for those without prior experience)