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Drug Safety Associate ( Rmp & Psur )

Naukri
Naukri
2-5 years
preferred by company
10 Dec. 22, 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

Drug Safety Associate – RMP & PSUR (Aggregate Reporting)

Company: Vizen Life Sciences
Industry: Pharmaceutical & Life Sciences
Employment Type: Full-Time, Permanent
Location: Hyderabad, Telangana, India
Experience Required: 2–5 Years
Education Required: B.Pharm / M.Pharm (Any Specialization)
Openings: 1


Job Overview

Vizen Life Sciences is hiring a skilled Drug Safety Associate – RMP & PSUR to support global pharmacovigilance operations with a strong focus on aggregate safety reporting. The role involves authoring, reviewing, and managing PSURs/PBRERs and Risk Management Plans (RMPs) in compliance with international regulatory standards.

This position is ideal for professionals with hands-on experience in aggregate reporting who are looking to advance their career within a structured, compliance-driven drug safety environment.


Key Responsibilities

Aggregate Safety Reporting

  • Author, review, and finalize Periodic Safety Update Reports (PSURs/PBRERs) and Risk Management Plans (RMPs) for global regulatory submissions

  • Ensure all aggregate reports meet regulatory, scientific, and quality standards and adhere to defined timelines

Literature Review & Data Validation

  • Conduct comprehensive literature searches to support PSUR and RMP development

  • Validate and assess data accuracy from scientific publications and safety sources

Data Extraction & Analysis

  • Extract, reconcile, and validate data from Reference Safety Information (RSI), sales data, prior reports, safety databases, and RMPs

  • Generate Line Listings (LLs) and supporting tables for inclusion in aggregate reports

Process & Delivery Management

  • Maintain and reconcile process trackers to ensure transparency and timely delivery

  • Support urgent and ad-hoc PSUR-related activities as required

Client & Stakeholder Interaction

  • Liaise with client stakeholders to resolve PSUR- and RMP-related queries

  • Ensure all deliverables align with client SOPs, regulatory expectations, and submission deadlines

Subject Matter Expertise & Mentorship

  • Act as a Subject Matter Expert (SME) for PSUR and RMP preparation

  • Provide training, guidance, and mentoring to junior team members on aggregate reporting processes


Required Skills & Competencies

  • Strong working knowledge of pharmacovigilance and aggregate reporting

  • In-depth understanding of PSUR/PBRER and RMP regulatory requirements

  • Experience with MedDRA coding and safety data interpretation

  • Hands-on exposure to Argus Safety or similar safety databases

  • Excellent analytical, documentation, and problem-solving skills

  • Strong written and verbal communication abilities

  • Proven ability to manage multiple projects and tight timelines

  • Collaborative mindset with strong cross-functional coordination skills


Preferred Technical Skills

  • Aggregate Reporting

  • PSUR / PBRER / RMP

  • Pharmacovigilance

  • Drug Safety Operations

  • MedDRA

  • Case Processing

  • Argus Safety

  • ITR / PV Processes


Education & Experience

  • Bachelor’s Degree: B.Pharm (Required)

  • Master’s Degree: M.Pharm (Preferred)

  • Experience: 2–5 years in Drug Safety, Pharmacovigilance, or Aggregate Reporting, with hands-on PSUR/RMP exposure


Why Join Vizen Life Sciences

Vizen Life Sciences provides a professional environment focused on quality, regulatory compliance, and continuous development. Employees gain exposure to global pharmacovigilance processes, client-facing responsibilities, and long-term career growth within the life sciences domain.


Disclaimer

This job description outlines the general scope and responsibilities of the role and may be subject to change based on business requirements. The company reserves the right to modify duties in alignment with organizational needs.