Sr. Associate Pharamocovigilance Operations

Amgen Technology Pvt Ltd.

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India - Hyderabad Until 8/22/2026 H-1B sponsor history First posted June 12, 2026 Last posted June 12, 2026
Job description

Career Category

Safety

Job Description

This position plays a role in the authoring, compilation and peer review of Amgen’s Periodic Aggregate Safety Reports (PASR) e.g. 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, and  country specific reports e.g. Korea PSUR, Brazil PSUR and Colombia Clinical Research Annual Safety Report Submission and Evaluation form. In compliance with global regulatory requirements. This role supports the end-to-end writing and documentation process and ensures timelines are met. 
 

Key Responsibilities:
Compilation and authoring of PASRs

•    Coordinate and schedule all meetings with cross-functional stakeholders to ensure effective collaboration and alignment
•    Drive report timelines and escalate risks or delays to team leads or management
•    Collaborate with cross-functional stakeholders and external business partners to collect PASR contributions and compile into PASR template.
•    Author safety content for all PASRs in collaboration with Therapeutic Area Safety scientists
•    Conduct peer QC of safety authored sections, coordinate Amgen review and resolve comments and initiate approval workflows.
•    Maintain and archive accurate records and documentation throughout the report process.
•    Review and approve published report versions (i.e. blinded, unblinded, EU FDA, Rest of World).
•    Manage report distribution to Contract Research Organizations (CROs) and Business Partners (BPs)
•    Ensure adherence to established timelines, regulatory guidelines and applicable standards, styles, guidelines and processes 
•    Peer review/quality review of all PASRs within established timelines with adherence to applicable guidelines and processes, using appropriate checklists 
•    Maintain and develop current 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

•    May assist with Literature Management activities as required

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About this role

Summary

Coordinate and author safety reports, ensure timeline adherence, collaborate with stakeholders, maintain regulatory compliance.

Job title

Sr. Associate Pharamocovigilance Operations

Experience level

null

Industry

pharmaceuticals

Location requirements

Hyderabad, India; on-site role only

Salary

Not specified

Visa sponsorship

H-1B sponsor history

Management role

No

Skills & keywords

Required skills

regulatory guidelinesPASRcollaborationdocumentationQC

Preferred skills

None specified

Specializations

safety reportsregulatory compliancepharmpvigilancePASRregulatory documents
Locations

Structured locations inferred from the posting.

Hyderabad, Telangana, India

On-site City