Clinical Research Associate - Entry (Shanghai)
Core
Conduct clinical monitoring visits for research sites to ensure compliance with protocols and regulatory requirements.
Role type
Entry-level Clinical Research Associate (CRA)
Builds
Clinical trial data integrity and regulatory compliance for biopharma and medical device clients
Domain
Clinical research / Biopharmaceuticals
Required skills
site monitoring, regulatory document review, source data verification, adverse event reporting, patient recruitment assessment, investigator qualification verification, inventory management, report writing
Preferred skills
study coordinator experience
Technologies
GCP, SOPs, Case Report Forms (CRF)
Responsibilities
Conduct qualification, initiation, monitoring, and closeout visits; Verify investigator qualifications and resources; Review medical records and source documentation against CRF data; Verify subject eligibility; Review regulatory documents; Manage investigational product accountability; Assess patient recruitment and retention; Complete monitoring reports and follow-up letters.
Seniority
Entry-level, training-focused IC
