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Sr. Associate Pharamocovigilance Operations

Amgen
3-7 years
INR 12 LPA – 22 LPA
Hyderabad
1 June 15, 2026
Job Description
Job Type: Full Time Education: M.Pharm/B.Pharm or M.Sc. Skills: Data Analysis, Document Management, Life Science, Regulatory Compliance, Waterfall Model, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding

Sr. Associate Pharmacovigilance Operations

Location: Hyderabad, Telangana, India
Company: Amgen
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 across global markets.


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, review, and integrate report contributions.

  • Ensure all reports comply with global pharmacovigilance regulations, internal procedures, and reporting standards.

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 collaboration to ensure timely completion of safety reporting activities.

  • Manage report distribution to external partners and vendors.

Quality Review & Documentation

  • Author safety content for aggregate reports in collaboration with Therapeutic Area Safety Scientists.

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

  • Coordinate review cycles, address reviewer 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 report lifecycle.

Regulatory Compliance & Quality Assurance

  • Ensure adherence to regulatory requirements, reporting timelines, company standards, and approved processes.

  • Perform peer reviews and quality reviews using approved checklists and procedures.

  • Maintain current knowledge of global pharmacovigilance regulations, industry standards, and emerging technologies.

  • Support inspection readiness and compliance initiatives.

Metrics & Performance Monitoring

  • Generate and maintain Periodic Aggregate Safety Report metrics.

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

  • Support process improvements and operational excellence initiatives.

Literature Management

  • Assist with literature management activities as required.

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


Required Qualifications

Education

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

Experience

  • 3–7 years of experience in Pharmacovigilance, Drug Safety, Aggregate Reporting, Medical Writing, or Regulatory Writing.

  • Experience with DSUR, PSUR, PBRER, SSUR, PADER/PAER, and other aggregate safety reports is preferred.

  • Experience working within pharmaceutical, biotechnology, or CRO environments.

Technical Skills

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

  • Experience in safety medical writing and aggregate report preparation.

  • Understanding of regulatory submission processes and safety documentation.

  • Strong quality review and compliance management skills.

  • Familiarity with pharmacovigilance systems and reporting tools.

Soft Skills

  • Excellent written and verbal communication skills.

  • Strong stakeholder management and cross-functional collaboration abilities.

  • High attention to detail and quality-focused mindset.

  • Strong project management and organizational skills.

  • Ability to manage multiple projects and deadlines simultaneously.