Clinical Research Coordinator Jobs in New Delhi at Max Healthcare for experienced clinical trial and ICH-GCP professionals.
Company Overview
Max Healthcare is one of India’s prominent hospital networks known for delivering advanced medical care and supporting high-quality clinical research programs. With a strong presence in Delhi and other major cities, Max Healthcare integrates patient care with research-driven innovation. The organization actively conducts investigator-initiated and sponsored clinical studies while maintaining strict adherence to ethical, regulatory, and safety standards. Clinical Research Coordinator Jobs in New Delhi
This opportunity is ideal for professionals seeking hands-on experience in hospital-based clinical trials while working closely with investigators, ethics committees, and patients in a regulated environment.
Job Location & Employment Type
- Job Location: New Delhi, India
- Employment Type: Full-Time, Permanent
- Industry: Hospital / Medical Services
- Department: Research & Development
Open Positions / Department Details
- Position: Clinical Research Coordinator (CRC)
- Experience Required: 1–4 Years
- Work Environment: Hospital-based clinical research unit
The selected candidate will support clinical trial execution from feasibility to close-out while ensuring regulatory compliance and patient safety. Clinical Research Coordinator Jobs in New Delhi
Key Roles & Responsibilities
1. Site Feasibility & Study Initiation
- Assist the Principal Investigator (PI) in evaluating study feasibility and operational readiness
- Support pre-study documentation and ensure regulatory preparedness before trial initiation
2. Regulatory Documentation & Compliance
- Collect and maintain updated CVs and essential documents of study personnel
- Prepare and organize required regulatory documentation such as financial disclosure forms, PI undertakings, and confidentiality agreements
- Coordinate submission packages for Institutional Review Board (IRB) or Institutional Ethics Committee (IEC) approvals
- Ensure timely submission of safety updates, protocol amendments, and periodic progress reports
3. Clinical Trial Coordination
- Support investigators during informed consent discussions with study participants
- Prepare for Site Initiation Visits (SIV) and monitoring visits
- Maintain and update Site Master File (SMF) and other essential trial documentation
- Organize screening logs and subject tracking records
4. Patient Recruitment & Data Handling
- Conduct pre-screening and screening activities as per protocol criteria
- Coordinate subject enrollment and follow-up visits (both in-person and telephonic)
- Assist in Case Report Form (CRF) completion and clinical data entry
- Prepare and maintain accurate source documents
5. Safety & Drug Accountability
- Support reporting and follow-up of Serious Adverse Events (SAEs)
- Maintain investigational product accountability logs and inventory records
6. Financial & Budget Tracking
- Assist in maintaining study budget records
- Monitor IRB fees, invoices, site administrative costs, laboratory expenses, and patient reimbursements
- Ensure financial documentation is aligned with study agreements
The role requires coordination between investigators, patients, sponsors, and regulatory authorities while maintaining compliance with ICH-GCP standards. Clinical Research Coordinator Jobs in New Delhi
Eligibility Criteria
Education
Candidates must hold one of the following qualifications:
- B.Pharm / M.Pharm / Pharm.D
- B.Sc / M.Sc in Life Sciences
- Any Graduate in relevant scientific disciplines
Experience
- 1 to 4 years of experience in clinical research or hospital-based clinical trials
Skills Required
- Strong knowledge of ICH-GCP guidelines
- Experience in IRB / IEC submissions and compliance management
- Understanding of SAE reporting and drug safety processes
- Hands-on experience with CRF completion and clinical data documentation
- Familiarity with patient recruitment and trial coordination
- Good organizational and communication skills
- Ability to manage multiple clinical tasks efficiently
Clinical Research Coordinator Jobs in New Delhi
Salary & Benefits
- Salary Range: INR 3.25 – 4.5 LPA (Approx.)
- Additional benefits and policies as per organizational norms
Selection Process
The hiring process may include:
- Resume shortlisting
- Technical or functional interview
- HR discussion
Final selection will be based on relevant experience, subject knowledge, and overall suitability.
How to Apply
- Mode of Application: Online Application
- Interested candidates should apply through the official recruitment link provided by the employer
No walk-in application process is mentioned for this role.
Important Dates
- Applications are open until positions are filled
Candidates are encouraged to apply early due to limited openings. Clinical Research Coordinator Jobs in New Delhi
Why Apply for This Pharma Job?
- Work within a reputed hospital research ecosystem
- Gain exposure to regulated clinical trials in a real-world patient setting
- Competitive salary package for CRC professionals
- Direct collaboration with experienced investigators and medical teams
- Strong focus on ethical research, compliance, and patient safety
- Excellent opportunity for career growth in clinical research operations
Important Note / Disclaimer
IndiaPharmaJobs.in is an independent job information platform and is not affiliated with Max Healthcare or its recruitment team. The above job information is shared for educational and informational purposes only. Candidates are advised to verify all details directly through the official company website before applying. Clinical Research Coordinator Jobs in New Delhi
Final Call-to-Action
If you have 1–4 years of clinical research experience and are looking to grow within a hospital-based research environment in Delhi, apply online for this Clinical Research Coordinator position at the earliest. Clinical Research Coordinator Jobs in New Delhi
