IQVIA, one of the world’s leading healthcare technology and clinical research organizations, is inviting applications for the position of Operations Specialist 1 โ Pharmacovigilance. This opportunity is ideal for professionals with 3โ6 years of Pharmacovigilance experience and strong expertise in Oncology ICSR case processing.
If you are looking to advance your career in drug safety, ICSR processing, and oncology pharmacovigilance, this IQVIA Pharmacovigilance job could be your next career move.
Job Overview
| Details | Information |
|---|---|
| Company | IQVIA |
| Position | Operations Specialist 1 |
| Department | Pharmacovigilance |
| Experience | 3โ6 Years |
| Location | Kochi, Kerala / Kolkata, West Bengal |
| Employment Type | Full-Time |
| Industry | Clinical Research / Pharmacovigilance |
Key Responsibilities
As an Operations Specialist 1 at IQVIA, you will:
- Process Individual Case Safety Reports (ICSRs) accurately and within timelines.
- Perform end-to-end pharmacovigilance case processing activities.
- Handle Oncology safety cases according to global regulatory requirements.
- Review, assess, and document adverse event information.
- Ensure compliance with company SOPs and global Pharmacovigilance regulations.
- Maintain high-quality standards in drug safety documentation.
- Collaborate with cross-functional teams to deliver quality pharmacovigilance services.
- Support continuous improvement initiatives within Pharmacovigilance operations.
Eligibility Criteria
Candidates should possess:
- Bachelor’s or Master’s degree in Pharmacy, Life Sciences, Nursing, Medicine, Biotechnology, or related healthcare discipline.
- 3โ6 years of Pharmacovigilance experience
- Strong experience in ICSR processing
- Mandatory experience in Oncology case processing
- Good understanding of global Pharmacovigilance regulations.
- Excellent communication and analytical skills.
- Ability to work in a quality-driven environment.
Preferred Skills
- Oncology Pharmacovigilance
- ICSR Case Processing
- Drug Safety Operations
- MedDRA Coding
- Argus Safety or similar PV databases
- Regulatory Compliance
- Quality Review
- Medical Terminology
- Attention to Detail
- Team Collaboration
Why Join IQVIA?
Working with IQVIA offers numerous career benefits, including:
- Opportunity to work with a global healthcare leader.
- Exposure to international Pharmacovigilance projects.
- Career growth in drug safety and clinical research.
- Collaborative work environment.
- Continuous learning and professional development.
- Opportunity to contribute to improving patient safety worldwide.
Salary
Based on current industry standards for professionals with 3โ6 years of Pharmacovigilance experience:
Estimated Salary: โน8,00,000 โ โน14,00,000 per annum (CTC)
Actual compensation will depend on experience, skills, and company evaluation.
How to Apply
Interested candidates can send their updated resume to:
Email: sherry.thammappakm@iqvia.com | Add Notice Period | CCTC, ECTC
Apply as early as possible, as positions may close once suitable candidates are shortlisted.