IQVIA is a global leader in clinical research, healthcare analytics, and commercial solutions for the life sciences industry. With a focus on accelerating drug development and improving patient outcomes, IQVIA provides data-driven insights and regulatory expertise to pharmaceutical and biotech companies worldwide.
📍 Location: Bangalore, India
📅 Last Date to Apply: July 28, 2025 (4 days left!)
🆔 Job Requisition ID: R1495142
Detailed Job Description
Job Overview
As a Regulatory Affairs Officer at IQVIA, you will:
✔ Prepare and review regulatory submissions for clinical trials and marketing approvals.
✔ Provide regulatory support for assigned projects under senior guidance.
✔ Ensure compliance with global regulatory guidelines (CMC, labeling, lifecycle maintenance).
Key Responsibilities
✅ Act as a Regulatory Team Member on small to medium projects.
✅ Track project timelines, manage workload, and implement client requests.
✅ Prepare and review regulatory documents (e.g., submissions, labeling, publishing).
✅ Participate in client meetings and assist in business development activities.
✅ Ensure adherence to standard operating procedures (SOPs) and suggest process improvements.
Required Skills & Qualifications
✔ Education:
- Bachelor’s or Master’s degree in Pharmacy, Life Sciences or related field.
✔ Experience: - Minimum 2 years in regulatory affairs (CMC, submissions, lifecycle management).
✔ Technical Skills: - Strong knowledge of R&D processes (preclinical, clinical, manufacturing).
- Proficiency in Microsoft Office & regulatory publishing tools.
✔ Soft Skills: - Excellent communication & organizational abilities.
- Ability to work on multiple projects with minimal supervision.
Benefits of Working at IQVIA
🔹 Global Exposure: Work with leading pharmaceutical & biotech companies.
🔹 Career Growth: Opportunities for professional development & certifications.
🔹 Work-Life Balance: Full-time role with structured work policies.
🔹 Cutting-Edge Projects: Contribute to innovative drug development & approvals.
How to Apply
