IQVIA Hiring Pharmacovigilance Scientist
Are you a pharmacovigilance professional with 2–3 years of experience looking to grow your career with a global healthcare leader? IQVIA, a top multinational company specializing in clinical research and healthcare analytics, is hiring Pharmacovigilance Scientists for its offices in Kochi and Thane. This is an excellent opportunity to join IQVIA’s dynamic Safety Aggregate Report and Analytics (SARA) team. IQVIA Hiring Pharmacovigilance Scientist
Whether you hold a degree in pharmacy, life sciences, or medicine, and have prior experience in aggregate safety reports or signal management, this role offers long-term career potential in the growing field of drug safety and pharmacovigilance.
About IQVIA
IQVIA is a global leader in advanced analytics, technology solutions, and contract research services for the life sciences industry. With operations in more than 100 countries, IQVIA supports pharmaceutical and biotech companies in accelerating clinical development, improving regulatory compliance, and enhancing healthcare decision-making. Its Safety Aggregate Report and Analytics (SARA) Center is at the forefront of ensuring drug safety and regulatory compliance worldwide. IQVIA Hiring Pharmacovigilance Scientist
Job Title: Pharmacovigilance (PV) Scientist
Location: Kochi & Thane
Experience: 2–3 Years
Job Type: Full-time, On-site
Education: B.Pharm, M.Pharm, Pharm.D, B.Sc, M.Sc, Life Sciences, Medicine
Last Date to Apply: June 27, 2025
Application Mode: Online
Job Summary
IQVIA is looking for skilled and motivated professionals to join its SARA team as Pharmacovigilance Scientists. In this role, you will lead the development and submission of safety aggregate reports, support signal detection activities, and manage literature surveillance for marketed and investigational products. IQVIA Hiring Pharmacovigilance Scientist
You will also collaborate with global regulatory bodies (e.g., FDA, EMA, PRAC) and internal stakeholders to ensure compliance with Good Pharmacovigilance Practices (GVP), ICH guidelines, and Standard Operating Procedures (SOPs).
Key Responsibilities
- Lead the preparation, review, and finalization of safety aggregate reports including PBRERs, PSURs, DSURs, PADERs, RMPs, and Addendum to Clinical Overviews (ACOs).
- Perform literature surveillance for new safety signals and product information.
- Act as a Signal Management Lead for both post-marketing and clinical trial projects.
- Prepare regulatory responses and support updates to product labels and RMPs.
- Ensure all reports and documentation meet Good Documentation Practices (GDP).
- Mentor and support junior team members as part of team development efforts.
- Collaborate with cross-functional teams such as Regulatory Affairs, Medical Safety, and Clinical Operations.
- Participate in internal audits, regulatory inspections, and compliance trainings.
- Contribute to technology-driven initiatives to improve pharmacovigilance systems and data analysis processes.
Required Qualifications
Candidates must meet the following eligibility criteria: IQVIA Hiring Pharmacovigilance Scientist
- A bachelor’s or higher degree in Life Sciences, Pharmacy, Medicine, or related disciplines.
- 2–3 years of hands-on experience in pharmacovigilance, safety report authoring, or signal management.
- In-depth knowledge of GVP, GCP, and ICH E2E pharmacovigilance guidelines.
- Familiarity with aggregate safety reporting timelines, templates, and processes.
- Excellent skills in MS Office Suite (Word, Excel, PowerPoint) for documentation and presentation.
- Strong written and verbal communication skills for interacting with global teams and regulatory authorities.
- Self-motivated, with excellent time management, problem-solving, and project coordination abilities.
Preferred Skills (Good-to-Have)
While not mandatory, the following competencies are desirable:
- Exposure to Regulatory Authorities’ requirements including EMA, FDA, PRAC.
- Hands-on experience in writing Risk Management Plans (RMPs) and Regulatory Briefing Documents.
- Ability to work in cross-functional teams and manage multi-country reporting projects.
- Prior experience working in CROs or pharmaceutical companies is a plus.
Why Join IQVIA?
Here are some compelling reasons to consider IQVIA for your next career move: IQVIA Hiring Pharmacovigilance Scientist
1. Global Impact
Work on international projects that directly contribute to public health and patient safety across the globe.
2. Career Advancement
IQVIA offers structured career development programs and continuous training to help you build expertise and leadership skills in pharmacovigilance.
3. Innovative Work Culture
Be a part of innovation-driven initiatives using advanced technologies such as automation, AI, and big data in pharmacovigilance.
4. Collaborative Environment
Work with professionals across departments like regulatory affairs, clinical research, and data management for end-to-end exposure to drug development.
5. Employee Benefits
Enjoy competitive compensation packages, flexible working hours, health insurance, and opportunities for global mobility.
Who Should Apply?
This role is ideal for:
- PV Associates or Scientists with 2–3 years of experience.
- Professionals experienced in authoring PBRER, DSUR, PSUR, or RMP.
- Life Sciences or Pharma graduates looking to transition into global roles.
- Candidates interested in regulatory safety writing and signal management.
How to Apply IQVIA Hiring Pharmacovigilance Scientist
Interested candidates can apply directly through the official IQVIA careers page or via verified job portals. Ensure your resume highlights relevant experience in pharmacovigilance, aggregate reports, and regulatory compliance. IQVIA Hiring Pharmacovigilance Scientist
Deadline to Apply: June 27, 2025
Final Thoughts
The Pharmacovigilance Scientist role at IQVIA offers a unique opportunity to work on impactful drug safety projects in a global setting. If you are passionate about patient safety and looking to grow within a leading CRO organization, this is the right time to make your move. IQVIA Hiring Pharmacovigilance Scientist
Apply now to become part of IQVIA’s SARA Center and shape the future of pharmacovigilance with innovation, compliance, and excellence.
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