Clinical Research Associate (PhD Candidates)
Core
Conduct on-site and virtual monitoring visits at clinical research sites to ensure compliance with protocols, verify data accuracy, and manage investigational product accountability for pharmaceutical and medical device trials.
Role type
Clinical Research Associate (CRA)
Builds
Clinical trial data integrity and regulatory compliance for biotechnology, pharmaceutical, and medical device companies
Domain
Clinical Research / Life Sciences
Deliverable
client delivery
Required skills
Protocol compliance, site monitoring, data verification, regulatory document review, adverse event reporting, patient recruitment assessment, inventory management
Preferred skills
PhD in health or science, 1+ years healthcare experience, travel adaptability, Microsoft Office proficiency
Technologies
Clinical Trial Management System (CTMS), 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; perform risk-based monitoring to identify deviations; verify subject eligibility; manage investigational product accountability; assess patient recruitment and retention success.
Seniority
Entry-level to Junior, training-focused IC