Clinical Research Associate - PhD in Life Sciences
Core
Conduct on-site and remote monitoring visits at clinical research sites to ensure compliance with protocols, GCP, and regulatory requirements for drug and medical device development.
Role type
Clinical Research Associate (CRA)
Builds
Clinical trial data integrity and regulatory compliance for pharmaceutical and medical device sponsors
Domain
Clinical research / Biopharmaceuticals / Medical devices
Deliverable
client delivery
Required skills
Protocol adherence, GCP knowledge, regulatory document review, adverse event verification, site qualification, data verification, risk-based monitoring
Preferred skills
PhD in Life Sciences, healthcare-related work experience, Microsoft Office proficiency, travel adaptability
Technologies
Clinical Trial Management System
Responsibilities
Conduct qualification, initiation, monitoring, and closeout visits; verify investigator qualifications and resources; review medical records and source documentation; monitor adverse events and drug accountability; assess patient recruitment and retention; complete monitoring reports.
Seniority
Entry-level to Junior, training-focused
