Fresher Pharmacovigilance Jobs | GSK PV Operations – ICSR Management
- GSK Hiring PV Ops Specialist I for ICSR Management | Pharmacovigilance Jobs in Bangalore
- Company Overview
- Job Role & Responsibilities
- Pharmacovigilance Operations
- Safety Data & Compliance
- Process Improvement & Team Support
- Eligibility / Qualifications
- Educational Qualification:
- Relevant Courses:
- Experience Required:
- Skills Required:
- Location & Salary
- Application Process
- Frequently Asked Questions (FAQs)
- 1. What is ICSR in pharmacovigilance?
- 2. Is prior experience mandatory?
- 3. What tools are used in this role?
- 4. What career growth can I expect?
- Summary
GSK Hiring PV Ops Specialist I for ICSR Management | Pharmacovigilance Jobs in Bangalore
A strong career opportunity is now open for professionals in pharmacovigilance and drug safety operations. Stiefel, a GSK company, is hiring a PV Ops Specialist I – ICSR Management in Bangalore.
This role is ideal for candidates with 2–7 years of experience in pharmacovigilance, especially those skilled in ICSR case processing, safety reporting, and regulatory compliance. The position offers excellent exposure to global drug safety operations, regulatory frameworks, and clinical research environments.
With 1 vacancy available, this is a high-value opportunity for professionals aiming to grow in pharmacovigilance operations, risk management, and global safety data management.
Company Overview
Stiefel, a GSK company, is part of GlaxoSmithKline, one of the world’s leading pharmaceutical and healthcare organizations. GSK is known for its strong presence in pharmaceuticals, vaccines, and consumer healthcare, with a mission to improve global health through innovation and scientific excellence.
With a strong regulatory and compliance-driven culture, GSK offers professionals the opportunity to work on global safety data, clinical trials, and drug development programs that impact millions of patients worldwide.
Job Role & Responsibilities
As a PV Ops Specialist I, you will play a key role in pharmacovigilance operations, focusing on ICSR management, safety reporting, and regulatory compliance.
Pharmacovigilance Operations
- Manage end-to-end ICSR case processing and reporting
- Monitor adverse event reports and ensure accurate documentation
- Perform data analysis for safety signals and risk assessment
- Maintain compliance with global pharmacovigilance regulations
Safety Data & Compliance
- Ensure adherence to GCP guidelines and regulatory requirements
- Maintain high standards of data quality and reporting accuracy
- Collaborate with clinical, regulatory, and safety teams
- Support audit readiness and compliance checks
Process Improvement & Team Support
- Identify process gaps and implement improvements in PV operations
- Provide training and support to team members
- Analyze trends and perform root cause analysis for safety issues
Eligibility / Qualifications
Educational Qualification:
B.Pharmacy, M.Pharmacy, Life Sciences, Biotechnology, Microbiology, Biochemistry, Medicine
Relevant Courses:
Pharmacovigilance, Drug Safety, Clinical Research, Regulatory Affairs, Pharmaceutical Sciences
Experience Required:
- 2 to 7 years in pharmacovigilance operations
- Experience in ICSR management preferred
Skills Required:
- Strong knowledge of pharmacovigilance regulations (GCP, global guidelines)
- Hands-on experience with Argus Safety or similar PV systems
- Analytical thinking and problem-solving skills
- Strong communication and teamwork abilities
- Ability to handle complex safety data and reporting requirements
Location & Salary
- Location: Bangalore, India
- Job Type: Full-time
- Salary: Not disclosed (competitive as per industry standards)
This role provides excellent exposure to global pharmacovigilance systems, making it a strong career step for professionals aiming for roles in drug safety, regulatory compliance, and clinical research operations.
Application Process
Interested candidates can apply through the official job listing:
Early application is recommended due to limited openings.
Frequently Asked Questions (FAQs)
1. What is ICSR in pharmacovigilance?
ICSR refers to Individual Case Safety Reports, which capture adverse event data related to drug safety.
2. Is prior experience mandatory?
Yes, 2–7 years of pharmacovigilance experience is required.
3. What tools are used in this role?
Argus Safety and other pharmacovigilance databases.
4. What career growth can I expect?
You can progress to roles like PV Specialist, Safety Scientist, or Drug Safety Manager.
Summary
| Category | Details |
|---|---|
| Company | Stiefel (GSK) |
| Vacancies | PV Ops Specialist I |
| Required Education | B.Pharm, M.Pharm, Life Sciences |
| Experience | 2–7 Years |
To apply for this job please visit www.naukri.com.
