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Introduction
The demand for drug safety professionals continues to grow as pharmaceutical companies focus on patient safety and regulatory compliance. The Pharmacovigilance Specialist job at ProPharma Group is an excellent opportunity for candidates with experience in adverse event case processing and drug safety operations. This role offers hands-on exposure to global pharmacovigilance practices, making it ideal for professionals aiming to build a long-term career in PV and clinical safety.
Job Overview
| Details | Information |
|---|---|
| Job Title | Pharmacovigilance Specialist |
| Company Name | ProPharma Group |
| Location | Hyderabad (Madhapur), India |
| Employment Type | Full-Time |
| Department | Pharmacovigilance / Drug Safety |
| Experience Required | 1–4 Years |
| Education | B.Pharm / Life Sciences |
| Salary | Not Disclosed |
Company Overview
ProPharma Group is a globally recognized organization specializing in regulatory, clinical research, and pharmacovigilance services. The company partners with pharmaceutical, biotechnology, and medical device organizations to ensure compliance, safety, and successful product lifecycle management. With a strong global presence, ProPharma offers dynamic career opportunities in drug safety and regulatory domains.
Job Location & Employment Type
This position is based in Hyderabad (Madhapur), a major hub for pharmacovigilance and clinical research operations in India. It is a full-time permanent role, offering stability and long-term career growth.
Open Positions / Department Details
The opening is within the Pharmacovigilance (PV) – Case Processing team, which is responsible for handling Individual Case Safety Reports (ICSRs), ensuring regulatory compliance, and maintaining drug safety standards.
Key Roles & Responsibilities
As a Pharmacovigilance Specialist, you will be responsible for managing safety data and ensuring compliance with global regulations. Key responsibilities include:
- Processing adverse event cases from clinical trials and post-marketing sources
- Coding medical data using MedDRA terminology
- Assessing seriousness, causality, and expectedness of adverse events
- Performing case follow-up activities to collect missing information
- Writing and reviewing detailed medical narratives
- Ensuring timely submission of cases to regulatory authorities
- Generating queries for incomplete or unclear case data
- Conducting peer reviews for quality and accuracy of cases
- Supporting training activities and knowledge sharing
- Keeping updated with global pharmacovigilance regulations
- Escalating discrepancies or concerns to senior PV team members
Eligibility Criteria
Education
- Bachelor’s degree in Life Sciences (Mandatory)
- B.Pharm preferred
- Advanced degree (Pharm.D, M.Pharm, RN) is an added advantage
Experience
- Minimum 1–4 years of experience in pharmacovigilance or drug safety
- Experience in case processing and ICSR handling is preferred
Skills Required
- Basic to intermediate knowledge of pharmacovigilance processes
- Familiarity with MedDRA coding and safety databases
- Strong attention to detail and data accuracy
- Excellent written and verbal communication skills
- Ability to multitask and manage deadlines
- Problem-solving and analytical thinking abilities
- Ability to work independently and within teams
Salary & Benefits
- Salary: Not Disclosed (As per company standards)
- Opportunity to work on global pharmacovigilance projects
- Exposure to international safety regulations and compliance frameworks
- Career growth in drug safety and regulatory domains
- Learning and development opportunities
Selection Process
The recruitment process generally includes:
- Resume screening
- HR interview
- Technical interview (Pharmacovigilance-focused)
- Final discussion
How to Apply
Interested candidates can apply through the online application process via the company’s official career portal or job listing platform.
Important Dates
- Application Status: Open (Apply early due to high competition)
Why Apply for This Job?
The Pharmacovigilance Specialist job at ProPharma Group offers a strong platform for professionals looking to grow in drug safety and clinical research. Key benefits include:
- Work with a globally recognized pharmacovigilance organization
- Gain hands-on experience in case processing and regulatory submissions
- Build expertise in MedDRA coding and safety data analysis
- Opportunity to work on international projects
- Strong career growth path in pharmacovigilance and regulatory affairs
This role is ideal for candidates aiming to specialize in drug safety and contribute to patient safety on a global scale.
FAQs
1. What does a Pharmacovigilance Specialist do?
A PV Specialist manages adverse event reports, ensures regulatory compliance, and maintains drug safety data accuracy.
2. Who can apply for this role?
Candidates with a life sciences or pharmacy background and 1–4 years of PV experience can apply.
3. Is MedDRA knowledge required?
Yes, basic knowledge of MedDRA coding is important for this role.
4. What is the salary for this position?
The salary is not disclosed but will be as per company standards.
5. How can I apply for this job?
You can apply online through the official company careers page or job portals.
Conclusion
The Pharmacovigilance Specialist role at ProPharma Group is a valuable opportunity for professionals seeking growth in drug safety and regulatory compliance. With global exposure, structured processes, and strong career prospects, this position is ideal for candidates aiming to advance in pharmacovigilance. Apply soon to secure your chance.
Disclaimer
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