Clinical Research Associate - Entry (Home-based)
Core
Conduct on-site clinical monitoring visits for research sites to ensure compliance with protocols, verify data accuracy, and manage investigational product accountability for pharmaceutical and medical device trials.
Role type
Entry-level Clinical Research Associate (CRA)
Builds
Clinical trial data integrity and regulatory compliance for pharma and medical devices
Domain
Clinical Research / Life Sciences
Required skills
Protocol compliance, site qualification, medical record verification, regulatory document review, adverse event reporting, patient recruitment assessment, inventory management
Preferred skills
Study coordinator experience, health/life science background, Microsoft Office proficiency
Technologies
Microsoft Office
Responsibilities
Conduct qualification, initiation, monitoring, and closeout visits; Verify investigator qualifications and resources; Review medical records and source documentation against case report forms; Monitor adverse events and serious adverse events; Assess patient recruitment and retention success; Complete monitoring reports and follow-up letters.
Seniority
Entry-level, training-focused IC
