Are you an experienced Pharmacovigilance professional looking to take the next step in your career? IQVIA — one of the world’s leading life science and clinical research organizations — is hiring a Pharmacovigilance Specialist 2 in Bengaluru, India.
This role is ideal for candidates with hands-on experience in clinical trial safety case processing, safety management planning, SAE processing, and ICH-GCP compliance. If you’re passionate about drug safety, regulatory reporting, and improving patient outcomes, this position could be the perfect next move.
🧪 Key Responsibilities
As a Pharmacovigilance Specialist II, you will:
- Perform end-to-end safety case processing including intake, triage, tracking, QC, and narrative writing
- Conduct regulatory reporting and reconciliation across trials
- Serve as Safety Management Lead for moderate to complex clinical studies
- Create safety documentation including Safety Management Plans (SMP) and SAE forms
- Participate in client meetings, investigator meetings, and training sessions
- Generate metrics, track timelines, and ensure compliance with scope and budget
- Mentor and guide junior pharmacovigilance staff
- Ensure compliance with ICH-GCP guidelines, SOPs, regulatory requirements and EDC systems
📌 Qualifications & Eligibility
To qualify, candidates must have:
✔ Bachelor’s degree in Life Sciences or healthcare discipline
✔ Minimum 3 years of experience in clinical safety or pharmacovigilance
✔ Strong understanding of ICH-GCP, regulatory reporting, and clinical research operations
✔ Proficiency in Microsoft Office and electronic data capture platforms
✔ Strong communication, analytical, and documentation skills
✔ Ability to manage priorities, work independently, and operate in a matrix environment
✔ Willingness to travel domestically and internationally when required
🎯 Preferred Skills
- Experience in safety oversight roles
- Strong medical terminology knowledge
- Ability to lead meetings and represent safety teams
- Strong attention to detail and problem-solving mindset
💼 Benefits of Working at IQVIA
- Exposure to global clinical research operations
- Opportunity to lead pharmacovigilance activities on major studies
- Professional growth and learning ecosystem
- Industry-leading digital tools and frameworks
📝 How to Apply
