Max Healthcare, one of India’s leading hospital networks, is hiring a Clinical Research Coordinator (CRC) for its New Delhi location. This opportunity is ideal for candidates with 1–4 years of clinical research experience who have strong knowledge of ICH-GCP guidelines, drug safety, IRB submissions, and clinical trial coordination.
If you are passionate about clinical trials, patient safety, and regulatory compliance, this role offers hands-on exposure to investigator-initiated and sponsored studies in a reputed hospital research environment.
Key Job Details
- Position: Clinical Research Coordinator
- Company: Max Healthcare
- Location: New Delhi, India
- Experience: 1 – 4 Years
- Salary: ₹3.25 – ₹4.5 LPA (Approx.)
- Employment Type: Full-Time | Permanent
- Industry: Medical Services / Hospital
- Department: Research & Development
Roles & Responsibilities – Clinical Research Coordinator
Site Feasibility & Study Start-Up
- Assist Principal Investigator (PI) in site feasibility assessments
- Support pre-trial documentation and regulatory readiness
Pre-Trial & Regulatory Documentation
- Collect and maintain updated CVs of site staff
- Ensure timely completion of:
- Financial Disclosure Forms
- PI Undertaking
- Confidentiality & Data Confidentiality Agreements
IRB / IEC Submission & Compliance
- Coordinate with IRB/IEC for faster approvals
- Timely submission of:
- Safety reports
- Protocol amendments
- Annual / six-monthly progress reports
Clinical Trial Operations
- Assist PI & Co-Investigators in Informed Consent Process
- Prepare for Site Initiation Visits (SIV)
- Maintain:
- Site Master File (SMF)
- Patient files & screening logs
Patient Recruitment & Data Management
- Pre-screening, screening, enrollment & subject recruitment
- CRF completion and clinical data entry
- Create source documents and templates
- Coordinate patient follow-up visits (physical & telephonic)
Safety & Drug Accountability
- SAE reporting and follow-up
- Drug accountability and inventory tracking
Financial & Budget Management
- Maintain study budget sheets
- Track:
- IRB fees & invoices
- Site administration fees
- Lab costs
- Patient reimbursements (travel, investigations, treatment)
Eligibility & Qualifications
- Education: Any Graduate (Life Sciences / Pharmacy preferred)
- Experience: 1–4 years in clinical research / clinical trials
- Mandatory Skills:
- ICH-GCP Guidelines
- IRB / IEC Submissions
- SAE Reporting & Drug Safety
- CRF Completion & Clinical Data Management
- Patient Recruitment & Site Coordination
Key Skills & Keywords
Clinical Research Coordinator, ICH-GCP, Clinical Trials, IRB Submission, SAE Reporting, Drug Safety, CRF, Clinical Data Management, Pharmacovigilance, Site Feasibility, Patient Recruitment, MedDRA, CTA, Clinical Research Jobs in Delhi
Why Join Max Healthcare?
- Work with one of India’s top hospital research ecosystems
- Exposure to regulated clinical trials
- Competitive salary and stable career growth
- Opportunity to work closely with experienced investigators
- Strong focus on patient safety and research quality
How to Apply
