CRC-Avacare
IQVIA · Shanghai, China
The apply link worked recently (not employer-confirmed).
Role summary
This position supports clinical research operations at a study site, assisting investigators with participant screening, protocol procedures, and regulatory documentation. Responsibilities include managing investigational products, coordinating site activities from initiation through closure, and maintaining accurate case report forms. Bachelor's degree in clinical medicine, pharmacy, nursing, or related health field required; prior clinical research experience preferred.
What they're looking for
- Bachelor's degree in clinical medicine, pharmacology, nursing, healthcare, or related medical field
- Clinical research experience preferred
- Knowledge of regulatory requirements and GCP guidelines
- Ability to manage study documentation and case report forms accurately
- Strong organizational and coordination skills for multi-site activities
What you'll be doing
- Support study initiation including feasibility assessments, ethics submissions, and site startup visits
- Assist with subject screening, enrollment, and follow-up visit coordination per protocol
- Manage investigational product inventory, study supplies, and laboratory samples at site
- Transcribe source data into case report forms and resolve data queries
- Participate in investigator meetings, monitoring visits, and audits as assigned
Privacy & handoff
This role links to IQVIA's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.