IQVIA Hiring Pharmacovigilance Specialist in Bengaluru | Pharmacovigilance Jobs
If you are searching for high-growth pharmacovigilance jobs, this IQVIA opening for a Pharmacovigilance Specialist 2 in Bengaluru is a standout opportunity. Designed for candidates eager to grow in clinical research jobs or transition into a rewarding life science job, this hybrid role lets you work on global safety case processing, ICH-GCP compliance, and advancesafety managementnt activities while shaping the future of clinical research.
- Location: Bengaluru, India
- Job Type: Full-time
- Job ID: R1511363
- Work Mode: Hybrid
About the Company:
IQVIA is a global leader in clinical research services, healthcare intelligence, and real-world data solutions. With a mission to accelerate medical advancement, IQVIA combines cutting-edge technology and deep scientific expertise to enhance drug development, improve patient outcomes, and support healthcare innovations across the world.
Job Overview:
The role delivers Safety Management Department services based on ICH-GCP guidelines, regulatory requirements, Novella SOPs, and project-specific procedures. Primary responsibilities include processing and reporting incoming safety events and related data. The Pharmacovigilance Specialist 2 also serves in a mentorship and leadership capacity, including functioning as a Safety Management Lead on moderate to large studies/programs with a moderate to complex scope of work.
Educational Requirements:
- A bachelor’s degree in life sciences, clinical research, or a licensed healthcare profession is required.
- Minimum 3 years of experience in clinical trial safety.
- Computer literacy with Microsoft Word and Excel; electronic data capture knowledge preferred.
- Strong verbal, written, organizational, and interpersonal skills.
- Ability to work independently, travel, prioritize, and perform in a matrix environment.
Key Responsibilities:
- Perform safety case processing tasks: intake, triage, completeness review, data entry, clinical narratives, queries, QC, reconciliation, metrics, and regulatory reports.
- Lead safety management for moderate to large studies.
- Conduct all start-up activities, including developing Safety Management Plans and SAE forms.
- Attend team meetings, investigator meetings, and present safety updates.
- Mentor and train new Safety Management staff.
- Ensure compliance with budgets, timelines, and project requirements.
- Identify, analyze, and resolve complex safety issues independently.
- Maintain proficiency in clinical research processes, medical terminology, ICH-GCP, and regulatory guidelines.
- Demonstrate professionalism, initiative, leadership, and strong customer service skills.
This role is a strong career accelerator for anyone aiming to build a powerful career in pharmacovigilance jobs, transition to advanced clinical research jobs, or secure a stable life science job with global exposure. Joining IQVIA offers not only professional growth but also the opportunity to work on high-impact safety programs that contribute to global patient safety.
