IQVIA has opened applications for the Safety Aggregate Report Spec 1 position in Bangalore, India. This opportunity is particularly relevant for pharmacovigilance professionals with experience in drug safety, aggregate reporting, signal management, or literature surveillance.
The IQVIA Safety Aggregate Report Specialist will work across important pharmacovigilance activities including PBRER/PSUR, DSUR, PADER, aggregate safety reports, literature surveillance, signal detection and regulatory safety responses. Candidates with approximately 1–2 years of relevant experience are preferred according to the official job description.
Applications are currently scheduled to close on 29 August 2026, so eligible candidates should consider applying promptly.
IQVIA Job Overview
Company: IQVIA
Job Title: Safety Aggregate Report Spec 1
Job Requisition ID: R1566157
Department: Lifecycle Safety / Pharmacovigilance
Location: Bangalore, India
Employment Type: Full Time
Experience: 1–2 years of relevant experience preferred
Qualification: Bachelor’s degree or equivalent combination of education, training and experience
Application Deadline: 29 August 2026
About the Role
The Safety Aggregate Report Specialist at IQVIA serves as an owner and contributor for safety aggregate reporting deliverables while ensuring compliance with applicable procedures, regulatory requirements and service-level agreements.
The position combines responsibilities across aggregate report writing, signal management, literature safety surveillance and pharmacovigilance support. The selected professional may act as an author, reviewer or quality checker for safety deliverables and collaborate with global project teams and clients.
Key Responsibilities
- Author, review and perform quality checks of safety aggregate reporting, signal management and literature surveillance deliverables.
- Lead and finalize small-to-medium aggregate safety reports.
- Prepare PBRERs/PSURs, DSURs, PADERs, ACOs, device reports and line listings.
- Prepare responses to regulatory authorities and Pharmacovigilance Risk Assessment Committee (PRAC) inquiries when required.
- Support ongoing literature safety surveillance for marketed and investigational medicinal products.
- Identify potential Individual Case Safety Reports (ICSRs) from scientific and medical literature.
- Evaluate events of special interest and perform aggregate safety data reviews.
- Contribute to literature deliverables supporting aggregate reporting and signal management activities.
- Conduct signal detection, signal validation and signal evaluation activities.
- Support proactive identification and characterization of emerging safety risks.
- Prepare signal management documentation and maintain appropriate signal tracking.
- Participate in safety management teams and communicate relevant findings.
- Prepare pharmacovigilance responses and supporting justification documents for regulatory and labeling activities.
- Coordinate with Medical Writing, Clinical Research, Regulatory Reporting, Safety Operations, Quality, QPPV and other cross-functional teams.
- Participate in audits and regulatory inspections when required.
- Maintain compliance with IQVIA and customer SOPs, work instructions and required training.
- Communicate project issues, metrics, client requests and SOW changes to appropriate stakeholders.
- Support project meetings, lessons-learned activities, technology initiatives and process innovation.
- Provide guidance, mentorship and training to less-experienced team members.
Qualifications
IQVIA requires a Bachelor’s degree, or an equivalent combination of education, training and relevant professional experience.
Candidates with educational backgrounds relevant to pharmacovigilance and life sciences may include qualifications such as B.Pharm, M.Pharm, Pharm.D, B.Sc/M.Sc Life Sciences, Biotechnology, Microbiology, Biochemistry, Clinical Research, Nursing, or other relevant healthcare and science degrees, subject to IQVIA’s eligibility assessment.
The official job description indicates that 1–2 years of prior relevant experience is preferred, particularly in:
- Drug safety / pharmacovigilance
- Aggregate reporting
- Signal management
- Literature surveillance
Skills Required
Candidates should have:
- Good knowledge of pharmacovigilance and medical terminology.
- Understanding of SOPs and work instructions relevant to drug safety activities.
- Knowledge or exposure to aggregate safety reports such as PSUR/PBRER, DSUR and PADER.
- Strong written and verbal communication skills.
- Good organizational and time-management capabilities.
- Excellent attention to detail and accuracy.
- Ability to manage multiple priorities and regulatory deadlines.
- Working knowledge of Microsoft Word, Excel and PowerPoint.
- Ability to follow procedures while working independently.
- Flexibility and willingness to develop skills across Lifecycle Safety functions.
Why Consider This IQVIA Pharmacovigilance Role?
This position provides exposure to several specialized areas of pharmacovigilance rather than focusing exclusively on individual case processing. Professionals can gain experience across aggregate reporting, signal detection and management, literature surveillance, regulatory safety responses and global safety operations.
Working with multidisciplinary teams may also provide exposure to Medical Safety, Regulatory Reporting, Clinical Research, Medical Writing, Quality and QPPV-related activities.
IQVIA is a global provider of clinical research services, healthcare intelligence and commercial insights to pharmaceutical, biotechnology and healthcare organizations.
Estimated Salary
IQVIA has not disclosed a salary range in the supplied job posting.
For structured-data purposes only, a reasonable market estimate for a Safety Aggregate Report Specialist-level position in Bangalore may be approximately ₹5,00,000–₹9,00,000 per year.
Important: This is an editorial market estimate and should not be interpreted as an official IQVIA salary offer. Actual compensation can vary according to experience, skills, current compensation, internal grading and company policy.
How to Apply
