Safety Aggregate Report Specialist at IQVIA, Bangalore | Apply Online
A rare chance has emerged for aspiring IQVIA Safety Specialist candidates in Bangalore. This Safety Aggregate Report Specialist role seeks candidates with 1–2 years of relevant experience in drug safety, aggregate reporting, or literature surveillance. Interested individuals are encouraged to apply before the deadline on 29 August 2026.
About the Company
IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. The organization focuses on creating intelligent connections to accelerate the development and commercialization of innovative medical treatments, ultimately aiming to improve patient outcomes and population health worldwide.
- Company: IQVIA
- Location: Bangalore, India
- Experience: 1–2 years of prior relevant experience preferred in drug safety, aggregate reporting, signal management, or literature surveillance
- Qualification: Bachelor’s degree or equivalent combination of education, training, and experience. B.Pharm / M.Pharm / Pharm.D / life sciences also typical.
- Posted: 28 August 2026
- Deadline: 29 August 2026
- Employment: FULL_TIME
IQVIA Safety Specialist Job Description
As an IQVIA Safety Specialist, the Safety Aggregate Report Specialist will serve as the principal owner of the SARA deliverable, ensuring compliance with all applicable service level agreements. Responsibilities include acting as the primary author or reviewer of SARA deliverables, leading and finalizing aggregate reports, and participating in safety management teams.
Key Responsibilities
- Act as primary author & reviewer/QCer of SARA deliverables involving aggregate reports, signal management, or literature review projects.
- Lead, author, and finalize small to medium aggregate reports including PBRERs/PSURs, DSURs, and device reports.
- Author responses to regulatory agency inquiries as required.
- Conduct ongoing literature safety surveillance for marketed and investigational products.
- Act as Signal Management Specialist on post-marketing and clinical trial projects.
- Participate in internal and external audits and inspections.
- Provide mentorship and training to less experienced resources.
- Communicate and document project issues to project team members and department management in a timely manner.
Eligibility Criteria
- Bachelor’s Degree in a relevant field.
- 1 – 2 years of prior relevant experience in drug safety, aggregate reporting, or literature surveillance.
- Good understanding of Standard Operating Procedures (SOPs) applicable to the role.
- Strong organizational and time management skills.
- Excellent attention to detail and accuracy.
- Ability to follow instructions and work independently.
- Proven ability to multi-task and manage competing priorities.
Required Skills
- Good working knowledge of Microsoft Office and web-based applications.
- Strong verbal and written communication skills.
- Self-motivated and flexible.
- Willingness and aptitude to learn new skills across all Lifecycle Safety service lines.
How to Apply
Interested candidates can apply through the official link:
Conclusion
This IQVIA Safety Specialist opportunity offers a pathway for qualified candidates to advance their careers in the pharmaceutical industry. Interested individuals are encouraged to apply before the deadline on 29 August 2026 to secure their chance for this role.
