Clinical Research Coordinator

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