Junior Clinical Research Associate - Clinical Study Coordinator Experience Required
Core
Conduct qualification, initiation, monitoring, and closeout visits at research sites in the DACH region to ensure compliance with protocols and regulations for drug and medical device development.
Role type
Junior Clinical Research Associate (CRA)
Builds
Clinical trial data integrity and regulatory compliance for pharmaceutical and medical device sponsors
Domain
Clinical Research / Life Sciences
Required skills
Clinical Research Coordinator experience, GCP knowledge, Protocol adherence, Site monitoring, Data verification, Adverse event reporting, Regulatory document review, Subject eligibility verification
Preferred skills
Life Science degree, German language proficiency, English language proficiency, Microsoft Office proficiency
Technologies
Clinical Trial Management System, Microsoft Office
Responsibilities
Conduct on-site and virtual monitoring visits; Verify investigator qualifications and resources; Review medical records and source documentation; Monitor adverse events and serious adverse events; Assess patient recruitment and retention; Complete monitoring reports and follow-up letters.
Seniority
Junior, entry-level CRA with prior coordinator experience
