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Sr. Associate Pharamocovigilance Operations

Amgen
3+ years
INR 12 LPA – 20 LPA
Hyderabad
1 June 15, 2026
Job Description
Job Type: Full Time Education: M.Pharm/B.Pharm or M.Sc. Skills: Clinical SAS Programming, Clinical Trials, Detail-Oriented, Drug Development, Lifesciences, Negotiation Skills, Regulatory Compliance, Communication Skills, CPC Certified, Data Analysis, Document Management, Life Science, Regulatory Compliance, Waterfall Model, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes

Sr. Associate Pharmacovigilance Operations

Location: Hyderabad, Telangana, India
Employment Type: Full-Time

Job Summary

The Sr. Associate Pharmacovigilance Operations is responsible for the authoring, compilation, review, and management of Periodic Aggregate Safety Reports (PASRs) in compliance with global regulatory requirements. This role supports the end-to-end safety reporting process, ensuring high-quality documentation, effective cross-functional collaboration, and timely delivery of aggregate safety reports.


Key Responsibilities

Periodic Aggregate Safety Report (PASR) Authoring & Compilation

  • Author, compile, and maintain Periodic Aggregate Safety Reports (PASRs), including:

    • Development Safety Update Reports (DSURs)

    • Periodic Benefit-Risk Evaluation Reports (PBRERs)

    • Periodic Safety Update Reports (PSURs)

    • Semi-Annual Safety Update Reports (SSURs)

    • Periodic Adverse Drug Experience Reports (PADERs/PAERs)

    • Device PSURs

    • Country-specific safety reports such as Korea PSUR, Brazil PSUR, and Colombia Clinical Research Annual Safety Reports.

  • Collaborate with Therapeutic Area Safety Scientists and cross-functional stakeholders to gather and integrate report contributions.

  • Ensure all reports are prepared in accordance with global regulatory requirements and company procedures.

Stakeholder Coordination & Project Management

  • Coordinate and schedule meetings with internal stakeholders, external business partners, and Contract Research Organizations (CROs).

  • Drive report timelines and proactively communicate risks, issues, or delays to management.

  • Facilitate effective collaboration to ensure timely completion of reporting activities.

Quality Review & Documentation

  • Author safety-related content for PASRs in collaboration with relevant stakeholders.

  • Conduct peer quality control (QC) reviews of safety-authored sections.

  • Coordinate review cycles, address comments, and manage approval workflows.

  • Review and approve published report versions, including blinded, unblinded, FDA, EU, and Rest-of-World submissions.

  • Maintain accurate, complete, and audit-ready documentation throughout the reporting lifecycle.

Compliance & Regulatory Support

  • Ensure adherence to established timelines, regulatory guidelines, company standards, and reporting procedures.

  • Perform quality reviews using approved checklists and processes.

  • Maintain current knowledge of pharmacovigilance regulations, industry standards, and technological advancements.

Metrics & Reporting

  • Generate and maintain Periodic Aggregate Safety Report metrics.

  • Monitor and report Key Compliance Indicators (KCIs) and Key Performance Indicators (KPIs).

  • Support continuous process improvement and compliance initiatives.

Literature Management

  • Assist with literature management activities as required.

  • Support literature review, tracking, and documentation processes related to pharmacovigilance activities.


Required Qualifications

  • Bachelor's or Master's degree in Pharmacy, Life Sciences, Biotechnology, Medicine, Nursing, or a related scientific discipline.

  • Experience in Pharmacovigilance, Drug Safety, Aggregate Reporting, Medical Writing, or Regulatory Writing.

  • Strong understanding of global pharmacovigilance regulations and aggregate safety reporting requirements.

  • Excellent written and verbal communication skills.

  • Strong organizational, project management, and stakeholder management abilities.

  • Ability to work effectively in a cross-functional and deadline-driven environment.