Looking to build a career in pharmacovigilance and drug safety reporting? IQVIA, a global leader in healthcare intelligence and clinical research, is hiring for two critical roles: Safety Aggregate Report Specialist 2 and Safety Aggregate Report Manager. These roles, based in Bangalore and Thane, India, involve leading safety aggregate reporting, signal management, and regulatory compliance. With application deadlines closing soon, this is the perfect opportunity to join one of the most respected names in the life sciences industry.
🧾 Job Overview
1. Safety Aggregate Report Specialist 2
- Location: Bangalore, India / Thane, Maharashtra
- Job ID: R1495489
- Experience Required: 3–4 years (preferred)
- End Date to Apply: September 26, 2025
The Specialist will serve as the principal owner of Safety Aggregate Report and Analytics (SARA) deliverables, including PBRERs/PSURs, DSURs, PADERs, RMPs, literature surveillance, and signal management.
2. Safety Aggregate Report Manager
- Location: Bangalore, India / Thane, Maharashtra
- Job ID: R1495179
- Experience Required: 4–6 years (preferred)
- End Date to Apply: September 26, 2025
The Manager role involves acting as a stand-alone global lead, overseeing large-scale aggregate reporting, regulatory submissions, audits, inspections, and mentoring junior staff.
🔑 Key Responsibilities
- Lead, author, and finalize safety aggregate reports (PBRERs, DSURs, RMPs, REMS, ACOs).
- Conduct literature surveillance for marketed and investigational products.
- Manage signal detection, validation, and evaluation to identify safety signals and mitigate risks.
- Prepare safety responses to regulatory authorities and PRAC inquiries.
- Ensure compliance with GVP, ICH, and global pharmacovigilance regulations.
- Mentor junior staff and contribute to departmental productivity metrics.
- Participate in audits, inspections, and client interactions.
🎓 Qualifications
- Bachelor’s degree in a Scientific or Healthcare discipline (Pharmacy, Life Sciences, or related).
- Specialist: 3–4 years of pharmacovigilance/aggregate reporting experience.
- Manager: 4–6 years of leadership experience in drug safety and regulatory reporting.
- Strong knowledge of ICH, GCP, GVP guidelines, medical terminology, and global PV regulations.
- Excellent organizational, communication, and report writing skills.
- Ability to work independently and manage multiple priorities under strict deadlines.
💼 Benefits of Working at IQVIA
- Competitive salary package (₹7.5 LPA – ₹16 LPA depending on role and experience).
- Exposure to global pharmacovigilance projects.
- Career growth with continuous training and mentoring.
- Opportunity to work with regulatory authorities worldwide.
- Inclusive, collaborative, and innovation-driven work culture.
📌 How to Apply
Application Link For Safety Aggregate Report Specialist 2
Application Link For Safety Aggregate Report Manager
