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Associate Manager, Pharmacovigilance (Pharmanovia)

8+ years
₹20 – ₹28 LPA
10 July 19, 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

Location: Mumbai, India (Hybrid: 3 days office, 2 days home)
Position: Associate Manager – Pharmacovigilance
Experience Required: 8+ years (including 4–5 years in aggregate safety reports & RMPs)
Company: Pharmanovia

About Pharmanovia:
Pharmanovia is a fast-growing, global specialty pharmaceutical company with a strong presence in over 160 markets and a portfolio of 20+ heritage brands. Founded in 2013, Pharmanovia revitalizes trusted medicines to improve global health outcomes. With a team spanning 29 nationalities across 12 countries, the company fosters a people-first culture built on integrity, agility, innovation, and long-term value creation.

Role Overview:
Pharmanovia is seeking an experienced Associate Manager – Pharmacovigilance to join its PV function in Mumbai. The role involves end-to-end authorship and oversight of aggregate safety reports, RMPs, ICSR compliance, and Safety Data Exchange Agreements (SDEAs), aligned with global pharmacovigilance standards.

Key Responsibilities:

  • Author aggregate safety reports including PADERs, SERs, SARs, and RMPs.

  • Manage and ensure compliance with SDEAs and ICSR submission timelines.

  • Support PV audits, regulatory inspections, and SOP implementation.

  • Lead internal process improvements in pharmacovigilance workflows.

  • Monitor regulatory intelligence and integrate updates into PV systems.

  • Contribute to product labeling updates based on safety profile evaluations.

  • Assist in PV risk assessments and due diligence activities.

  • Track and report pharmacovigilance KPIs to senior leadership.

  • Collaborate cross-functionally with internal stakeholders to align PV operations with business strategies.

Candidate Requirements:

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

  • 8+ years of pharmacovigilance experience; at least 4–5 years in aggregate report and RMP authorship.

  • Strong expertise in SDEAs, ICSR review, and compliance monitoring.

  • Familiarity with local and global PV regulations.

  • Experience with core pharmaceutical companies is highly desirable.

  • Excellent problem-solving, time management, and communication skills.

  • Demonstrated adaptability, resilience, and leadership potential.

What We Offer:

  • Competitive salary and annual performance bonus.

  • Hybrid work environment with flexibility (3 days in-office, 2 remote).

  • Health & wellness programs, pension scheme, and employee recognition.

  • Opportunities for professional development in a global PV landscape.

How to Apply:
Interested candidates can apply via Pharmanovia’s careers portal or connect with their HR team directly.

Estimated Salary: ₹20 – ₹28 LPA (based on PV leadership roles with global scope and 8+ years of experience in Mumbai)