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Site Care Partner

8-12 years
₹18,00,000 – ₹28,00,000 per annum
10 Aug. 13, 2025
Job Description
Job Type: Full Time Education: MBBS/MD Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Site Care Partner
Location: Mumbai, India

Company Overview:
Pfizer is a global leader in biopharmaceutical innovation, dedicated to breakthroughs that change patients’ lives. Through world-class research, development, and partnerships, Pfizer delivers life-changing medicines and vaccines across therapeutic areas. Our purpose-driven culture and four core values—Courage, Excellence, Equity, and Joy—guide everything we do.

Why Join Pfizer:

  • Work at the forefront of global clinical research and development.

  • Collaborate with multidisciplinary teams to accelerate study timelines.

  • Competitive compensation, comprehensive benefits, and career growth opportunities.

  • Inclusive workplace with global reach and local impact.

Position Summary:
The Site Care Partner serves as Pfizer’s primary point of contact for investigative sites throughout the study lifecycle. This role is accountable for site start-up through activation, relationship building, recruitment support, and safeguarding quality and patient safety at the site level. The position requires cross-functional collaboration to optimize site performance and ensure timely study delivery.

Key Responsibilities:

  • Lead site start-up activities, including Pre-Trial Assessment (PTA), site initiation, informed consent document finalization, and activation checklist completion.

  • Provide local insights for country and site selection, protocol feasibility, and medical practice reviews.

  • Maintain strong relationships with investigator sites and site organizations, addressing issues promptly to uphold Pfizer’s reputation.

  • Collaborate with CRAs, study managers, and regulatory teams to ensure monitoring readiness and timely First Subject First Visit (FSFV).

  • Develop and execute recruitment plans aligned with global and local targets.

  • Support study conduct by reviewing site reports, managing escalations, and ensuring compliance with GCP, ICH guidelines, and country-specific regulations.

  • Participate in close-out activities, ensuring quality and consistency in study delivery.

  • Contribute to supply chain coordination for investigational product (IP) and ancillary materials.

Qualifications:

  • Graduate or Postgraduate in Pharmacy, Biotechnology, or Nursing; MBBS/MD preferred.

  • 8–12 years of experience in site management, monitoring, and study start-up through close-out.

  • Strong knowledge of GCP, ICH guidelines, and local regulatory requirements.

  • Proficiency in English; local language skills preferred.

  • Excellent communication, presentation, and relationship-building skills.

  • Ability to travel nationally and internationally as required.

Salary Range: ₹18,00,000 – ₹28,00,000 per annum (estimated for senior site management roles in India).