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.
🏢 About the Company
Pfizer is a leading global biopharmaceutical company dedicated to discovering, developing, and delivering innovative medicines that improve patient health worldwide. The company follows rigorous global pharmacovigilance and safety standards, ensuring patient safety throughout the product lifecycle. Working at Pfizer provides exposure to international drug safety systems, structured PV processes, and continuous learning opportunities
📊 Job Details
- 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 Functions – 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.
🎓 Eligibility Requirements
Candidates applying for this role must meet the following mandatory criteria:
- Education:
- B.Pharm / M.Pharm / Pharm.D ONLY
- Experience:
- 0–2 years of experience in:
- Pharmacovigilance
- Drug Safety
- Safety Data Management
- 0–2 years of experience in:
- Freshers with strong foundational drug safety knowledge are encouraged to apply
🧠 Required Skills
- Strong focus on accuracy and consistency in safety data processing
- Ability to carefully review and validate safety‑related information
- Solid analytical thinking for case assessment support
- Ability to identify issues and contribute to problem resolution
⭐ ⭐ Role Breakdown
The Safety Data Management Specialist role is a foundational position within pharmacovigilance operations. For freshers, it offers hands‑on exposure to real‑world safety data workflows, global compliance standards, and collaborative drug safety environments. Experience in this role builds strong fundamentals for long‑term careers in pharmacovigilance, regulatory safety, and clinical operations.
🎯 Suitable Applicants
This opportunity is suitable for:
- Pharmacy freshers (B.Pharm / M.Pharm / Pharm.D)
- Candidates with 0–2 years of PV or drug safety experience
- Graduates interested in safety data and patient safety roles
- Individuals seeking entry‑level positions in global pharma companies
📈 Career Progression
With experience and strong performance, professionals can progress into roles such as:
- Pharmacovigilance Associate
- Drug Safety Specialist
- Safety Case Processing Associate
- Senior Safety Data Management roles
Pfizer also supports continuous learning and internal career advancement.
💰 Expected Pay
Salary for this role depends on experience, skills, and company standards.
Compensation will be offered based on candidate experience and interview performance.
💡 Application Tips
- Highlight analytical skills and willingness to learn during interview
- Revise pharmacovigilance fundamentals and safety data concepts
- Strengthen knowledge of medical terminology and drug safety processes
- Practice attention‑to‑detail and documentation accuracy
🔗 Application Process
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.
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📚 Career Guide
❓ FAQs-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.
