Experienced CRA - Berlin (with Sign-On Bonus)
Core
Conduct qualification, initiation, monitoring, and closeout visits for research sites to ensure compliance with protocols and regulatory requirements.
Role type
Experienced Clinical Research Associate (CRA)
Builds
Clinical trial data integrity and site compliance for biotechnology, pharmaceutical, and medical device companies
Domain
Clinical Research / Life Sciences
Deliverable
physical/clinical work
Required skills
Clinical site monitoring, Protocol adherence, GCP knowledge, Medical record verification, Adverse event reporting, Investigator qualification, Regulatory document review, Patient recruitment assessment
Preferred skills
Microsoft Office proficiency, Time management, Detail-oriented approach
Technologies
Microsoft Office
Responsibilities
Conduct qualification, initiation, monitoring, and closeout visits for research sites; Verify investigator qualifications, training, and resources; Review medical records and source documentation against CRF data; Verify investigator enrollment of eligible subjects; Review regulatory documents and manage medical device/investigational product accountability; Assess patient recruitment and retention success.
Seniority
Mid-level, hands-on IC
