Experienced Clinical Research Associate, Home based
Core
Conduct clinical monitoring visits at research sites to ensure protocol compliance, data accuracy, and regulatory adherence for clinical trials.
Role type
Clinical Research Associate (CRA)
Builds
Clinical trial data integrity and regulatory compliance
Domain
Clinical Research / Biopharmaceuticals
Deliverable
physical/clinical work
Required skills
Clinical trial monitoring, Protocol compliance, GCP knowledge, Medical record verification, Adverse event reporting, Site qualification, Regulatory document review, Patient recruitment assessment
Preferred skills
CRA certification, Microsoft Office proficiency, Strong communication skills
Technologies
Microsoft Office
Responsibilities
Conduct qualification, initiation, monitoring, and closeout visits at research sites; Verify investigator qualifications and resources; Review medical records and source documentation against case report forms; Verify subject eligibility; Review adverse events and concomitant medications; Assess patient recruitment and retention; Complete monitoring reports and follow-up letters.
Seniority
Mid-level, experienced IC
