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Lead - Clinical Research, (Rwe) Medical Affairs

Sun Pharma
7-12 years
INR 40 LPA – 55 LPA
Mumbai, India
1 June 18, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: HCPCS Level II, ICD-10-CM, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICD-10-PCS, ICH guidelines

Lead – Clinical Research (Real World Evidence & Medical Affairs)

Department: Medical Affairs
Location: Mumbai (Sun House – Corporate Office)
Reporting To: General Manager – Medical Affairs, India
Team Size: 4 Direct Reports
Education: MD Pharmacology (Mandatory)
Experience: 7–12+ Years in Medical Affairs / Clinical Research / RWE


About the Role

The Lead – Clinical Research (RWE) will be responsible for the strategic planning, execution, oversight, and governance of Real World Evidence (RWE), non-regulatory clinical studies, investigator-initiated studies (IIS), registries, observational studies, and related research programs across India. The role will ensure compliance with GCP, ICMR guidelines, applicable regulations, and organizational policies while driving evidence generation to support medical and business objectives.

The incumbent will lead clinical research operations, manage CROs and investigators, oversee study budgets, drive operational excellence, and build a high-performing research team.


Key Responsibilities

1. Clinical Research Strategy & Evidence Generation

  • Lead the design, planning, and execution of Real World Evidence (RWE) studies.

  • Develop and implement evidence-generation strategies aligned with therapeutic area priorities.

  • Drive observational studies, registries, epidemiological studies, PRO studies, EMR studies, IIS, and non-regulatory interventional studies.

  • Partner with Medical Affairs, Commercial, Regulatory, and Global teams to identify evidence gaps and research opportunities.

  • Support publication planning and scientific dissemination activities.


2. Study Governance & Compliance

  • Develop, review, and maintain SOPs, work instructions, templates, and study governance processes.

  • Ensure compliance with:

    • ICH-GCP Guidelines

    • ICMR Ethical Guidelines

    • NDCT Rules & applicable Indian regulations

    • Pharmacovigilance requirements

    • Internal quality standards

  • Maintain Trial Master Files (TMF) and study documentation.

  • Manage audits, inspections, CAPAs, and quality improvement initiatives.

  • Conduct risk assessments and develop mitigation strategies for all ongoing studies.


3. Clinical Study Management

  • Oversee study feasibility, site selection, investigator engagement, and study initiation.

  • Review and approve:

    • Study protocols

    • Case Report Forms (CRFs)

    • Informed Consent Documents (ICDs)

    • Investigator Brochures (IBs)

    • Clinical Study Reports (CSRs)

    • Safety narratives and related study documents

  • Monitor study progress, timelines, recruitment, data quality, and deliverables.

  • Ensure timely study completion within approved timelines and budgets.

  • Present and defend protocols before regulatory and ethics committees when required.


4. CRO & Vendor Management

  • Identify, evaluate, onboard, and manage CROs and research vendors.

  • Establish performance metrics and governance frameworks for external partners.

  • Conduct periodic CRO performance and compliance assessments.

  • Ensure vendors adhere to Sun Pharma quality, compliance, and pharmacovigilance requirements.

  • Drive operational excellence through effective vendor oversight and issue resolution.


5. Investigator & Site Management

  • Develop and maintain relationships with key investigators and research institutions.

  • Conduct site feasibility assessments and investigator selection.

  • Support execution of confidentiality agreements, clinical trial agreements, and financial contracts.

  • Lead investigator meetings and study-related training programs.

  • Ensure protocol adherence and GCP compliance across participating sites.


6. Safety & Pharmacovigilance Oversight

  • Ensure timely reporting of:

    • Serious Adverse Events (SAEs)

    • SUSARs

    • Safety notifications

  • Collaborate with Pharmacovigilance teams to maintain regulatory compliance.

  • Ensure safety data collection, review, reconciliation, and reporting activities are completed accurately and on time.


7. Data Management & Study Reporting

  • Collaborate with data management and biostatistics teams.

  • Drive data quality, query resolution, and database lock activities.

  • Review statistical analysis plans and study reports.

  • Ensure generation of high-quality study reports and publications.

  • Develop and maintain study dashboards and management reports.


8. Financial & Budget Management

  • Develop and manage annual clinical research budgets.

  • Monitor study expenditures and forecast resource requirements.

  • Ensure optimal utilization of research investments.

  • Manage investigator payments, CRO budgets, and vendor contracts.


9. Stakeholder Management

  • Serve as the primary point of contact for internal and external stakeholders.

  • Collaborate closely with:

    • Medical Affairs

    • Regulatory Affairs

    • Pharmacovigilance

    • Clinical Operations

    • Legal

    • Finance

    • Procurement

  • Build strong partnerships with KOLs, investigators, CROs, and academic institutions.


10. People Leadership & Talent Development

  • Lead, mentor, and develop a high-performing clinical research team.

  • Establish performance goals and development plans.

  • Drive succession planning and capability building.

  • Foster a culture of accountability, collaboration, and continuous improvement.


Key Performance Indicators (KPIs)

  • On-time study initiation and completion

  • Recruitment and retention performance

  • Budget adherence

  • Audit and inspection outcomes

  • Data quality metrics

  • Publication outputs

  • Investigator engagement scores

  • CRO performance metrics

  • Team development and retention


Required Qualifications

Education

  • MD Pharmacology (Mandatory)

  • Additional certification in Clinical Research or GCP preferred

Experience

  • 7–12+ years in Medical Affairs, Clinical Research, or Clinical Operations

  • Proven experience managing Real World Evidence (RWE) studies

  • Experience managing CROs and multi-center studies

  • Prior people management experience preferred