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IQVIA, a global leader in clinical research and life sciences analytics, is inviting applications for two exciting pharmacovigilance positions:
- Safety Aggregate Report Specialist 2 (Bangalore, Thane)
- Manager, Safety Operations Team (Pune)
If you’re a Pharma or Life Sciences professional seeking to advance your career in drug safety and regulatory reporting, this is your chance to work with one of the most respected CROs in the world.
🔬 Position 1: Safety Aggregate Report Specialist 2
📍 Locations: Bangalore, Karnataka | Thane, Maharashtra
🕒 Employment Type: Full-time
🗓️ Application Deadline: November 5, 2025
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Key Responsibilities
- Author and finalize aggregate safety reports such as PBRERs, PSURs, DSURs, PADERs, and RMPs.
- Conduct literature safety surveillance and support signal detection for marketed and investigational products.
- Lead Signal Management activities and ensure timely detection and documentation of safety signals.
- Coordinate with cross-functional teams like Regulatory Affairs, Real-World Evidence, Medical Writing, and Clinical Operations.
- Ensure compliance with Good Pharmacovigilance Practice (GVP) and ICH guidelines.
- Mentor junior safety professionals and contribute to innovation and quality improvement initiatives.
Qualifications
- Bachelor’s degree in Life Sciences, Pharmacy, or related discipline (Master’s preferred).
- 3–4 years of experience in aggregate reporting, signal management, or pharmacovigilance.
- Strong understanding of global regulatory requirements, including GVP and GCP.
- Excellent command over medical writing, data analysis, and project management.
- Proficiency in MS Office, safety databases, and Good Documentation Practices (GDP).
🧭 Position 2: Manager – Safety Operations Team
📍 Location: Pune, Maharashtra
🕒 Employment Type: Full-time
🗓️ Application Deadline: November 5, 2025
Key Responsibilities
- Manage a team of safety operations professionals to deliver case processing and aggregate reports.
- Conduct regular reviews on project performance, deliverables, and team metrics.
- Collaborate with senior management on staffing, forecasting, and operational excellence.
- Lead internal audits, training sessions, and performance improvement initiatives.
- Drive business outcomes by aligning pharmacovigilance operations with client needs.
Qualifications
- Bachelor’s degree in Life Sciences or related field.
- 5–7 years of total experience, including at least 3–4 years in pharmacovigilance and team leadership.
- Proficient in project finance, resource planning, and metric-based performance evaluation.
- Strong communication, problem-solving, and leadership skills.
- Flexibility to operate in shifts and manage multiple projects concurrently.
💼 Benefits of Working at IQVIA
- Competitive salary and performance-based incentives.
- Opportunities to work on global pharmacovigilance projects.
- Access to advanced analytics tools and safety databases.
- Continuous learning through mentorship and certification programs.
- Inclusive, innovation-driven workplace culture.
📨 How to Apply
Application Link for Safety Aggregate Report Specialist 2
Application Link for Manager – Safety Operations Team
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