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Associate Manager

8+ years
₹22 – ₹30 LPA
10 Aug. 6, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science 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

Associate Manager – Pharmacovigilance
📍 Location: Mumbai, India (Hybrid – 3 days office, 2 days home)
🕒 Experience: 8+ Years (including 4–5 years in aggregate reports & RMPs)
💼 Industry: Pharmacovigilance / Regulatory Affairs
🏢 Company: Pharmanovia

Salary: ₹22 – ₹30 LPA (Estimated based on seniority and industry benchmarks in Mumbai)


About the Role:
Pharmanovia is looking for a seasoned Associate Manager – Pharmacovigilance to join its growing PV team. This role focuses on aggregate report authoring, ICSR oversight, and regulatory compliance across global and local levels. You'll be an integral part of a company that revitalizes iconic medicines to improve lives worldwide.


Key Responsibilities:

  • Author aggregate safety reports such as PADERs, SERs, and SARs

  • Prepare and maintain Risk Management Plans (RMPs)

  • Strategically manage SDEAs, ensuring regulatory compliance and operational effectiveness

  • Ensure compliance with ICSR timelines and partner obligations

  • Support audits and inspections by regulatory bodies

  • Develop and optimize internal PV processes and SOPs

  • Monitor and implement regulatory intelligence updates

  • Contribute to product labeling updates aligned with benefit-risk assessments

  • Participate in PV risk assessments and due diligence for new partnerships/products

  • Report and track KPIs to senior leadership for performance monitoring

  • Collaborate cross-functionally with leadership and business units


Qualifications & Experience Required:

  • Bachelor's in Pharmacy (Master’s degree preferred)

  • 8+ years of PV experience with minimum 4–5 years in aggregate reports & RMPs

  • Proven experience in SDEA management and ICSR compliance

  • Strong command of local and global PV regulations

  • Prior exposure in core pharmaceutical companies preferred

  • Excellent problem-solving, organizational, and time management skills

  • Technically proficient and adaptable


What Pharmanovia Offers:

  • Competitive salary + bonus + benefits

  • Health & wellness programs

  • Recognition awards & social events

  • Pension scheme

  • Hybrid working (3 office + 2 home days/week)

Be part of a purpose-driven team working across Cardiovascular, Oncology, Endocrinology, and Neurology, where your contribution will impact lives globally. If you're agile, meticulous, and ready to step into a high-impact PV role, this is your opportunity.