Regulatory Affairs Jobs | IQVIA is Hiring | Apply Online
Looking for exciting Life Sciences Jobs with a global healthcare leader? IQVIA Careers has announced an opportunity for the position of Analyst – Regulatory Intelligence in Bengaluru. This role is ideal for professionals with expertise in drug safety, pharmacovigilance, and regulatory compliance who are seeking rewarding Regulatory Affairs Jobs in the pharmaceutical and healthcare industry.
- Job Title: Analyst – Regulatory Intelligence
- Location: Bengaluru, India
- Type: Full-time | Hybrid
- Job ID: R1550739
About the Company
IQVIA is a global provider of clinical research services, healthcare intelligence, and commercial insights for the life sciences industry. The company supports pharmaceutical, biotechnology, and healthcare organizations with data-driven solutions that accelerate innovation and improve patient outcomes. Operating across numerous countries, IQVIA combines advanced analytics, technology, and scientific expertise to help organizations navigate complex healthcare challenges. Its services span clinical development, regulatory intelligence, market access, and healthcare consulting, making it one of the most recognized names in the life sciences sector.
Key Responsibilities
- Prepare, review, and update regulatory documentation in Drug Safety & Pharmacovigilance, focusing on the APAC region, USA, and Canada.
- Monitor and analyze regulatory updates issued by relevant bodies in the territory.
- Work within cross-functional teams to ensure the production and maintenance of high-quality regulatory intelligence related to clinical trials.
- Perform quality control activities of external expert contributions within clinical trials.
- Provide knowledge related to safety to support inquiries from customers, sales, marketing, and business development.
- Act as a subject matter expert of Regulatory knowledge in Drug Safety.
- Understand the scope of work, deliverables, and manage workload accordingly.
- Conduct regulatory training sessions for small groups or individuals within the RI team.
Education
Master’s degree in Life Sciences.
Skills Required
- Proven experience in managing Drug Safety submissions within Life Sciences in the USA, Canada, and APAC region.
- Hands-on experience in drug safety submissions like ICSR and periodic submissions, RMP, Signal, Literature review.
- In-depth knowledge of Drug Safety & Pharmacovigilance regulations.
- Ability to assess the impact of new regulatory requirements.
- Experience in writing summaries/reports for different audiences.
- Strong attention to detail, proactive and organized.
- Knowledge of quality management within Life Sciences.
- Strong software and computer skills, including Microsoft Office and AI tools like Copilot.
- Self-motivated and enthusiastic with the ability to work on several projects.
Professionals looking for specialized Regulatory Affairs Jobs should consider this opportunity under IQVIA Careers. The Analyst – Regulatory Intelligence position offers valuable exposure to global regulations, pharmacovigilance practices, and healthcare intelligence operations. For candidates seeking long-term growth in Life Sciences Jobs, this role provides an excellent platform to build expertise while contributing to global healthcare and regulatory excellence.
