Freshers Pharmacovigilance Jobs at Pfizer Healthcare
- Pfizer Hiring Associate Safety Data Management Specialist in Chennai | Freshers Pharmacovigilance Jobs
- Company Overview
- Job Role & Responsibilities
- Key Responsibilities:
- Eligibility / Qualifications
- Educational Background:
- Experience Required:
- Skills Required:
- Location & Salary
- Application Process
- Why This Role Matters in Pharma Industry
- Frequently Asked Questions (FAQs)
- 1. Is this role suitable for freshers?
- 2. What is ICSR processing?
- 3. What database is used?
- 4. What career growth can I expect?
- Summary
Pfizer Hiring Associate Safety Data Management Specialist in Chennai | Freshers Pharmacovigilance Jobs
A high-demand opportunity is now open for freshers and early-career professionals in pharmacovigilance. Pfizer is hiring Associate Safety Data Management Specialists in Chennai for its Worldwide Medical and Safety division. This role is ideal for candidates with 0–2 years of experience who want to build a career in drug safety, ICSR processing, and global pharmacovigilance operations.
This position focuses on adverse event reporting, safety data analysis, and regulatory compliance, making it one of the most sought-after entry-level roles in the pharmaceutical industry.
Company Overview
Pfizer is one of the world’s leading biopharmaceutical companies, known for developing innovative medicines and vaccines that improve global health outcomes. With a strong presence in clinical research, drug development, and safety monitoring, Pfizer operates across multiple regulated markets worldwide.
The company’s pharmacovigilance division plays a critical role in ensuring the safe and effective use of medicines through continuous safety monitoring and regulatory compliance.
Job Role & Responsibilities
As an Associate Safety Data Management Specialist, you will be responsible for handling safety data and processing adverse event reports.
Key Responsibilities:
- Monitor drug, biologics, and medical device safety surveillance programs
- Intake, evaluate, and process adverse event reports from clinical trials and post-marketing sources
- Perform Individual Case Safety Report (ICSR) processing using Argus Safety database
- Assess case validity, perform duplicate checks, and prioritize cases
- Code adverse events and products using standard medical coding practices
- Conduct causality and seriousness assessments for reported cases
- Draft case narratives and perform follow-ups for missing information
- Review cases for accuracy, completeness, and regulatory compliance
- Analyze medical literature and support regulatory submissions
Eligibility / Qualifications
Educational Background:
B.Pharmacy, M.Pharmacy, Pharm.D
Experience Required:
- 0–2 years of experience in pharmacovigilance or drug safety
Skills Required:
- Strong understanding of pharmacovigilance and ICSR processes
- Knowledge of medical terminology and regulatory requirements
- Attention to detail and analytical skills
- Good communication and teamwork abilities
- Familiarity with Argus Safety database (preferred)
Location & Salary
- Location: Chennai, India
- Work Mode: Hybrid
- Job Type: Full-time
- Salary: As per industry standards
This role offers excellent career growth in pharmacovigilance, drug safety, and regulatory affairs, which are among the most stable and high-paying domains in the pharmaceutical industry.
Application Process
Interested candidates can apply through the official link below:
Candidates are encouraged to apply early as fresher pharmacovigilance roles are highly competitive.
Why This Role Matters in Pharma Industry
Safety data management specialists play a crucial role in monitoring adverse drug reactions and ensuring patient safety. Their work helps regulatory authorities make informed decisions about drug safety and effectiveness.
This role is essential in maintaining trust in pharmaceutical products and supporting global healthcare systems.
Frequently Asked Questions (FAQs)
1. Is this role suitable for freshers?
Yes, this role is open for candidates with 0–2 years of experience.
2. What is ICSR processing?
It involves handling Individual Case Safety Reports related to adverse drug reactions.
3. What database is used?
Argus Safety database is commonly used in pharmacovigilance.
4. What career growth can I expect?
You can grow into roles such as Drug Safety Associate, PV Specialist, or Safety Scientist.
Summary
| Category | Details |
|---|---|
| Company | Pfizer |
| Vacancies | Associate Safety Data Management Specialist |
| Required Education | B.Pharmacy, M.Pharmacy, Pharm.D |
| Experience | 0–2 Years |
To apply for this job please visit pfizer.wd1.myworkdayjobs.com.
