S3 Clinical Research is a leading Site Management Organization (SMO) dedicated to advancing clinical trials with a patient-centric approach. With a strong commitment to quality, integrity, and regulatory compliance, S3 Clinical Research collaborates with pharmaceutical companies, CROs, and investigators to facilitate smooth clinical trial operations.
🔹 Why Join S3 Clinical Research?
✔ Work on cutting-edge clinical trials
✔ Be part of a growing SMO in India
✔ Opportunity to enhance your career in clinical research
Detailed Job Description
Job Title: Clinical Research Coordinator / Site Manager
📍 Locations: Ahmedabad & Jamnagar, Gujarat
🏢 Workplace Type: On-site
🕒 Job Type: Full-time
Key Responsibilities:
- Oversee day-to-day clinical trial operations at the site.
- Coordinate with Principal Investigators (PIs), sponsors, and CROs for smooth trial execution.
- Ensure protocol compliance, accurate documentation, and patient safety.
- Manage study logistics, site staff training, and patient follow-ups.
- Maintain regulatory and GCP compliance throughout the trial.
Who Should Apply?
✅ Educational Qualification:
- M.Pharm / M.Sc in Clinical Research (or related field).
- Prior experience as a CRC or Site Manager is preferred.
✅ Skills Required:
- Strong organizational & communication skills.
- Ability to manage multiple trials independently.
- Knowledge of ICH-GCP guidelines & clinical trial protocols.
Benefits & Career Growth
✔ Competitive salary package
✔ Hands-on experience in multicentric clinical trials
✔ Opportunity to work with leading pharma companies & CROs
✔ Career advancement in clinical research & site management
How to Apply?
📩 Send your CV to: HR.s3clinicalresearch@gmail.com
📌 Subject Line: “Application for CRC/Site Manager – [Your Name]”
🚀 Early applications preferred! Limited openings available.
