Pfizer Hiring Fresher for Safety Data Management Specialist: PV Jobs 2026
Pfizer, a global biopharmaceutical leader, is hiring for the role of Safety Data Management Specialist (Pharmacovigilance) at its Chennai location. This opportunity is suitable for candidates with 0–2 years of experience and a background in B.Pharm, M.Pharm, or PharmD, who are looking to build a career in drug safety and pharmacovigilance operations.
The role focuses on safety data management activities, including case processing, data quality checks, regulatory compliance, and safety database operations. Candidates will work within a regulated global environment, supporting pharmacovigilance processes aligned with international standards.
This position offers strong exposure to global safety operations, structured learning, and long‑term career growth within Pfizer’s pharmacovigilance ecosystem.
Job Overview
- Position: Safety Data Management Specialist
- Department:PV
- Location: Chennai, India
- Experience: 0 to 2 Years
- Qualification: B.Pharm, M.Pharm, Pharma.D
- Job Type: Full-Time
Key Responsibilities – Safety Data Management Specialist
- Safety Surveillance Operations: Monitor the company’s drug, biologics, and medical device safety surveillance program in line with global pharmacovigilance standards.
- Adverse Event Intake & Processing: Receive, assess, and process adverse event reports for both clinical trial and post‑marketing activities.
- Case Assessment & Workflow Management: Review case information and determine the appropriate workflow for safety case processing based on defined criteria.
- Structured Task Execution: Perform assigned activities within a structured, procedure‑driven environment, following established workflows and SOPs.
- Supervised Decision‑Making: Resolve issues within defined options, with guidance and oversight from supervisors as required.
- Quality & Accuracy Assurance: Ensure work outputs are reviewed regularly for accuracy, completeness, and sound technical judgment.
- Regulatory Support: Provide support to project teams by applying regulatory requirements and corporate policies for safety and regulatory submissions.
- Safety Data Analysis Support: Assist Worldwide Strategy and Regulatory teams by analyzing post‑marketing safety data, reviewing medical literature, and supporting related safety activities.
Required Skills & Qualifications
- Education: B.Pharm, M.Pharm, or Pharm.D only.
- Experience: 0–2 years of experience in pharmacovigilance, drug safety, or safety data management.
- Core Skills
- Strong attention to detail to ensure accuracy in safety data processing.
- Solid analytical skills for case assessment and problem resolution.
- Good written and verbal communication skills.
- Ability to collaborate effectively within cross‑functional teams.
- Willingness to learn continuously and adapt to evolving PV processes.
- Pharmacovigilance Knowledge: Completion of a pharmacovigilance course or certification, or good knowledge of medical terminology and global drug safety regulations.
- Scientific Exposure: Publications in peer‑reviewed scientific journals.
- Digital & AI Skills
- Experience using AI tools, including generative technologies such as ChatGPT or Microsoft Copilot, to support problem solving and improve productivity.
- Curiosity to explore responsible and ethical use of AI, including risk management and compliance considerations.
Why Join PFizer?
- Global Biopharmaceutical Leader
- Join one of the world’s most respected biopharmaceutical companies, working in a highly regulated environment that supports patient safety and global healthcare innovation.
- Strong Foundation in Pharmacovigilance
- Gain hands‑on experience across safety data management, ICSR processing, regulatory compliance, and safety surveillance for drugs, biologics, and medical devices.
- Structured Learning & Growth
- Pfizer offers continuous learning opportunities, structured onboarding, and exposure to global safety practices—supporting long‑term career growth in pharmacovigilance and drug safety operations.
- Cross‑Functional Global Collaboration
- Work closely with Worldwide Safety, Regulatory, Clinical, and Strategy teams, gaining exposure to global workflows and international safety standards.
- Technology‑Driven Environment
- Engage with advanced safety databases, digital tools, and evolving AI‑supported workflows, strengthening technical and analytical capabilities.
How to Apply
Interested candidates should apply only through the official company career website using the link provided below.
Important Disclaimer
This job post is shared for informational purposes only, based on publicly available job details. Candidates are advised to verify eligibility, job responsibilities, and application procedures from the official IQVIA website before applying.
Similar Job for fresher : Thermo fisher Hiring Fresher for Clinical Resource Analyst
FAQ-Safety Data Management Specialist
1. Who can apply for this role at Pfizer?
Candidates with B.Pharm, M.Pharm, or Pharm.D qualifications and 0–2 years of experience in pharmacovigilance or drug safety can apply.
2. Is this role suitable for freshers?
Yes. This role is suitable for freshers and early‑career professionals who want to build a foundation in safety data management and pharmacovigilance.
3. What are the main responsibilities in this role?
You will support adverse event intake, ICSR case processing, duplicate checks, coding, narrative writing, listedness and causality assessment, and ensure compliance with global safety requirements.
4. Will I work on both clinical trials and post‑marketing safety data?
Yes. The role involves handling clinical trial safety cases as well as post‑marketing adverse event reports.
5. Which safety systems or databases will I use?
You will work with pharmacovigilance safety databases, processing cases, updating information from XML sources, and ensuring data accuracy and regulatory compliance.
