Overview
Clinical Research Coordinator I (CRC I) in Mumbai, supporting day-to-day coordination and execution of clinical trials while ensuring participant experience, safety, and protocol compliance.
What you'll do
- Coordinate and execute clinical trial activities per study protocols, ICH-GCP, applicable CDSCO/ICMR guidance, and site SOPs.
- Support participant recruitment, pre-screening, enrollment, scheduling, retention, and follow-up.
- Conduct protocol-required participant visits and ensure participant safety and protocol compliance.
- Obtain and document informed consent according to study requirements and institutional policies.
- Process, prepare, and ship laboratory specimens per protocol and lab guidelines.
- Maintain source/regulatory documentation, update CTMS and eCRFs, and enter data into EDC systems.
- Support sponsor monitoring visits, audits, and regulatory inspections; maintain study regulatory files.
What you'll need
- 1–3 years of clinical research, healthcare, or hospital experience.
- Working knowledge of ICH-GCP guidelines and Indian clinical research regulations.
- Bachelor's or Master's degree in life sciences, pharmacy (B.Pharm/PharmD), nursing, biotechnology, allied health sciences, or a related discipline.
- Strong organizational skills and attention to detail.
- Effective verbal and written communication skills in English.
- Proficiency with Microsoft Office applications.
- Centralized and/or multi-site support experience is preferred (not required).
Details
- Location: Mumbai, India.
- Compensation: ₹12 lakh to ₹17 lakh.
- Travel: Willingness to travel to other sites in India upon request.
Read the full description and apply on the company’s own careers page.
