Instagram
youtube
Facebook

Periodic Report Specialist

0-2 years
Not Disclosed
10 Sept. 15, 2025
Job Description
Job Type: Full Time Education: B.Sc/ M.Sc/ M.Pharm/ B.Pharm/ Life Sciences 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

Position: Safety – PASR Authoring & Review
Location: India – Hyderabad
Work Type: On Site
Job ID: R-224802
Date Posted: Sep 10, 2025
Category: Safety

Position Overview:
This role is responsible for the authoring, compilation, and peer review of Amgen’s Periodic Aggregate Safety Reports (PASRs), including but not limited to:

  • Development Safety Update Report (DSUR)

  • Periodic Benefit-Risk Evaluation Report (PBRER) / Periodic Safety Update Report (PSUR)

  • Semi-Annual Safety Update Report (SSUR)

  • Periodic Adverse Drug Experience Report (PADER/PAER)

  • Device PSUR

  • Country-specific reports (e.g., Korea PSUR, Brazil PSUR, Colombia Clinical Research Annual Safety Report)

The position ensures compliance with global regulatory requirements and supports the end-to-end writing and documentation process, meeting all required timelines.


Key Responsibilities:

PASR Compilation & Authoring

  • Coordinate and schedule meetings with cross-functional stakeholders to ensure alignment.

  • Drive report timelines; escalate risks or delays to team leads or management.

  • Collaborate with internal teams and external partners to gather PASR contributions and compile them into standardized templates.

  • Author safety content for all PASRs in collaboration with Therapeutic Area Safety scientists.

  • Conduct peer quality control (QC) of authored sections and manage Amgen review, comment resolution, and approval workflows.

  • Maintain accurate records and documentation throughout the report process.

  • Review and approve published report versions (blinded, unblinded, EU, FDA, Rest of World).

  • Manage report distribution to Contract Research Organizations (CROs) and Business Partners (BPs).

  • Ensure compliance with timelines, regulatory guidelines, and internal standards and processes.

  • Peer review all PASRs using appropriate checklists to ensure quality and adherence to guidelines.

  • Maintain up-to-date knowledge of regulatory guidelines, technological advances, and industry standards.

  • Generate PASR metrics, including Key Compliance Indicators (KCIs) and Key Performance Indicators (KPIs).

Literature Management Process

  • Support Literature Management activities as required.