Job Description

Position of Clinical Research Coordinator

1. Clinical Trials & Industry Liaison

Act as the single-point interface between the hospital and: Multinational & Indian pharmaceutical companies Medical device manufacturers CROs, SMOs, academic research networks Global research sponsors and innovation partners Proactively identify, attract, and onboard clinical trials, including: Phase II, III, and IV trials Investigator-Initiated Trials (IITs) Post-marketing surveillance (PMS) studies Device and diagnostic trials Registries, observational studies, real-world evidence studies Build and maintain long-term strategic relationships with research wings of pharma and device companies in India and globally.

2. Feasibility & Site Readiness

Conduct trial feasibility assessments including: Patient pool analysis Investigator interest and capability Infrastructure and equipment readiness Regulatory and operational feasibility Coordinate with consultants, clinicians, nursing, pharmacy, lab, radiology, ICU, and OT teams to assess trial suitability. Prepare feasibility questionnaires, site capability documents, and responses for sponsors and CROs.

3. Ethics Committee & Regulatory Coordination

Act as the nodal coordinator between: Investigators / consultants Institutional Ethics Committee (IEC) Sponsors and CROs Manage: Ethics submissions, amendments, renewals, SAE reporting Regulatory documentation as per ICMR, CDSCO, DCGI, GCP, ICH guidelines Ensure strict compliance with ethical, legal, and regulatory standards at all times.

4. Study Operations & Execution

Oversee end-to-end study lifecycle: Study initiation and site activation Patient recruitment and screening coordination Informed consent process oversight Protocol adherence and deviation management Monitoring visits, audits, and inspections Ensure timely data collection, documentation, and query resolution. Coordinate with study monitors, auditors, and regulatory inspectors.

5. Academic Research & Fellowship Programs

Support and structure research activities for postgraduate fellowship programs, including: Thesis planning and execution Investigator-initiated studies Publications, abstracts, and conference presentations Mentor clinicians and fellows in: Research methodology Protocol writing Data management and publication ethics Drive a culture of academic research and innovation within the hospital.

6. New Research Initiatives & Growth

Identify emerging research opportunities, new molecules, new devices, and innovative study designs. Assist hospital leadership in: Developing a long-term clinical research strategy Positioning the hospital as a preferred research site Revenue generation through sponsored trials Maintain a pipeline of upcoming trials and collaborations.

Eligibility & QualificationsMandatory Qualifications

MPharm / PharmD / MSc (Clinical Research / Pharmacology / Life Sciences)OR PhD in Pharmacology, Clinical Research, Life Sciences, or allied fields

Experience

Minimum 3-7 years of experience in: Clinical research coordination CRO / pharmaceutical company research division Hospital-based clinical trials unit Hands-on experience with sponsored trials, IITs, and ethics committee processes is essential.

Knowledge & Skills

Strong working knowledge of: ICH-GCP guidelines ICMR and CDSCO regulations Ethics committee functioning Clinical trial documentation and compliance Excellent stakeholder management and communication skills Ability to interact confidently with: Senior consultants and investigators Sponsors, CROs, and global research teams High level of organisational, analytical, and problem-solving ability Strong presentation, negotiation, and relationship-building skills

Contact

: 6290917626 or subham.barman@superhealth.co.in

Job Type: Permanent

Pay: ?11,343.41 - ?50,000.00 per month

Benefits:

Provident Fund
Work Location: In person