Clinical Research Associate - Entry (Beijing)
Core
Conduct qualification, initiation, monitoring, and closeout visits for clinical research sites to ensure compliance with protocols and regulations.
Role type
Entry-level Clinical Research Associate (CRA)
Builds
Clinical trial data integrity and regulatory compliance for biotechnology, pharmaceutical, and medical device companies
Domain
Clinical Research / Clinical Trials
Required skills
Site monitoring, regulatory document review, medical record verification, adverse event reporting, patient recruitment assessment, investigational product accountability
Preferred skills
Study coordinator experience, therapeutic area knowledge
Technologies
GCP, SOPs, Case Report Forms (CRF)
Responsibilities
Conduct site qualification, initiation, monitoring, and closeout visits; Verify investigator qualifications and resources; Review regulatory documents and medical records; Monitor adverse events and investigational product inventory; Assess patient recruitment and retention; Complete monitoring reports and follow-up letters.
Seniority
Entry-level, training-focused IC
