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.
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Canada |Quebec :
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