NETCOLLAB TECHNOLOGIES PRIVATE LIMITED is hiring an experienced Clinical Research Coordinator (CRC) to manage and execute hospital-based clinical studies across Delhi NCR. This is a full-time, on-site clinical research job with direct exposure to investigators, hospital teams, and medical innovation projects.
The role is ideal for professionals with 2+ years of clinical research experience who are confident working in hospital environments, handling clinical documentation, and ensuring compliance with GCP, ICMR, and regulatory guidelines.
🔬 Job Overview – Clinical Research Coordinator (CRC)
- Job Title: Clinical Research Coordinator
- Location: Delhi / Gurugram (On-site, hospital-based)
- Employment Type: Full-Time
- Experience Required: More than 2 years
- Salary: ₹50,000 – ₹70,000 per month
- Reporting To: Management Team
🧪 Key Roles & Responsibilities
Clinical Study Coordination
- Coordinate day-to-day execution of clinical studies at hospital sites
- Ensure strict adherence to approved protocols, SOPs, GCP, and regulatory requirements
- Support study start-up, initiation, monitoring visits, and close-out activities
- Act as the primary liaison between investigators, ethics committees, sponsors, and internal teams
Patient & Investigator Support
- Assist investigators in patient screening, enrollment, and follow-ups
- Coordinate the informed consent process ethically and compliantly
- Maintain strong collaboration with clinicians, nurses, radiology, OT staff, and hospital administration
Clinical Data & Documentation Management
- Maintain accurate CRFs, source documents, screening and enrollment logs
- Ensure data integrity, traceability, and audit/inspection readiness
- Resolve data queries and discrepancies in coordination with investigators
Device & Procedure Support (If Applicable)
- Support clinical use of medical devices during procedures
- Coordinate with clinical and technical teams for correct device usage
- Record procedural details and device-related clinical observations
Reporting & Communication
- Share regular study status updates and site reports with stakeholders
- Escalate protocol deviations, safety concerns, or compliance issues
- Support audits, internal training, and process improvement initiatives
🎓 Educational Qualifications
- Bachelor’s or Master’s degree in:
- Life Sciences
- Biotechnology
- Clinical Research
- Pharmacy
- Nursing
- Biomedical Engineering
- or related disciplines
✅ Preferred Experience & Skills
- Prior experience as a Clinical Research Coordinator / Clinical Trial Coordinator
- Hands-on experience in hospital-based clinical studies or medical device trials
- Strong knowledge of GCP, ICMR guidelines, and regulatory documentation
- Excellent communication, coordination, and documentation skills
- High attention to detail and ability to manage multiple study sites
- Willingness to travel across hospital locations
🌟 Why Join Netcollab Technologies?
- Direct involvement in impactful clinical research and medical innovation
- Exposure to reputed hospitals and experienced clinicians
- Strong learning curve and long-term career growth in the medical technology sector
- Opportunity to contribute to improved patient care and clinical outcomes