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Periodic Report Specialist

5-9 years
Not Disclosed
10 July 31, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc/B.harm/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

 

Job Title:
Periodic Report Specialist

Location:
Hyderabad, India

Job Summary:
Amgen is hiring a Periodic Report Specialist to lead the authoring, compilation, and review of Periodic Aggregate Safety Reports (PASRs) including DSURs, PBRERs, PSURs, PADERs, and country-specific reports. This on-site role in Hyderabad is ideal for professionals with 5–9 years of experience in pharmacovigilance and safety report writing, who are looking to work in a fast-paced, global regulatory environment.


Key Responsibilities:

  • Author and compile PASRs including DSURs, PBRERs/PSURs, PADERs, and local reports (e.g., Korea PSUR)

  • Coordinate meetings and timelines with global stakeholders

  • Drive timely collection and integration of content from cross-functional teams

  • Review and perform peer QC of safety sections

  • Manage report review workflows and resolve stakeholder comments

  • Approve and distribute finalized reports to CROs and business partners

  • Ensure compliance with global regulatory guidelines and internal SOPs

  • Conduct literature management activities as required

  • Generate and report key compliance metrics (KPIs/KCIs)


Required Skills & Qualifications:

  • 5–9 years of total professional experience

  • Minimum 2–3 years in writing periodic safety reports

  • Bachelor’s or Master’s degree in Life Sciences or Pharmacy

  • Strong understanding of global safety reporting standards (e.g., PBRER, PSUR, PADER)

  • Excellent knowledge of ICH guidelines and pharmacovigilance processes

  • Experience with peer reviews, regulatory timelines, and safety content QC

  • Familiarity with metrics reporting (KPI/KCI)


Perks & Benefits:

  • Opportunity to work with a globally recognized biopharmaceutical leader

  • Exposure to international safety reporting requirements and systems

  • Collaborative work environment with cross-functional global teams

  • Professional development and continuous learning opportunities

  • Competitive compensation and benefits package


Company Description:
Amgen is a leading global biotechnology company dedicated to advancing innovative therapies and enhancing patient outcomes worldwide. With a strong commitment to science and safety, Amgen empowers its teams to deliver excellence in compliance, quality, and innovation.


Work Mode:
On-site – Hyderabad, India


Call-to-Action:
Are you ready to advance your pharmacovigilance career with a global leader in biotech? Apply now and be a part of Amgen’s mission to ensure safety and regulatory excellence in patient care.