IQVIA Hiring Operations Specialist 1 – Pharmacovigilance jobs | Bengaluru
Looking to break into global pharmacovigilance jobs with one of the world’s most trusted clinical research organizations? IQVIA is offering an exciting opportunity for life science graduates and PV professionals to join their team as Operations Specialist 1. If you’re passionate about drug safety and clinical research processes and want to work on high-impact projects, this role places you at the center of the healthcare innovation ecosystem.
About the Company (IQVIA):
IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services for the life sciences industry. With operations worldwide, IQVIA accelerates biomedical innovation and supports pharmaceutical companies in bringing safer, effective treatments to patients. The organization is known for its powerful combination of technology, data, and human expertise, making it one of the most preferred workplaces for professionals seeking clinical research jobs and life science jobs.
Job Overview:
IQVIA is looking for skilled and motivated candidates with experience in LSMV or ArisG Safety Databases. The role involves reviewing, assessing, and processing safety data as per global regulations, SOPs, and project-specific guidelines. You will work closely with cross-functional teams to ensure timely, high-quality PV deliverables.
- Position: Operations Specialist 1
- Work Location: Bengaluru, India
- Mode: Office-based
- Job Type: Full-time
Educational Requirements:
- Bachelor’s degree in Life Sciences, biomedical sciences, healthcare, or allied fields
- Up to 3 years of experience in pharmacovigilance or drug safety
- Strong knowledge of medical terminology and safety databases (ArisG/LSMV)
Key Responsibilities:
- Process and review safety data in compliance with global PV regulations
- Perform case intake, AE tracking, coding, narrative writing, and literature surveillance
- Manage case data entry and ensure timely updates in the safety database
- Support medical review of non-serious AEs/ADRs
- Maintain 100% compliance with project SOPs and quality standards
- Collaborate with project management, clinical, medical monitors, and data management teams
- Identify quality issues and escalate appropriately
- Mentor new team members (if assigned)
- Participate in team meetings and departmental initiatives
Skills Required:
- Proficiency in ArisG / LSMV databases
- Strong knowledge of pharmacovigilance workflows
- Excellent communication and documentation skills
- Ability to multitask, prioritize, and meet strict deadlines
- Strong analytical ability and attention to detail
- Willingness to learn and adapt to dynamic PV processes
- Team-player mindset with willingness to support cross-functional groups
If you’re passionate about enhancing patient safety, building a strong career foundation, and joining one of the most recognized names in life sciences, IQVIA offers the perfect platform. This is your opportunity to level up your career in pharmacovigilance jobs while working alongside global experts.
