IQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. With a focus on driving healthcare forward, IQVIA empowers professionals to deliver groundbreaking medical solutions through data-driven insights and regulatory expertise.
📌 Why Join IQVIA?
✔ Global impact in pharmaceutical & healthcare innovation
✔ Inclusive & diverse work culture
✔ Career growth with industry-leading training
📌 Job Title: Regulatory Affairs Officer 2
📍 Location: Bangalore / Mumbai / Homebased (Remote)
📅 Job Type: Full-time
📋 Job Description
As a Regulatory Affairs Officer 2 at IQVIA, you will play a pivotal role in ensuring compliance with global clinical trial regulations. You will collaborate with cross-functional teams to prepare, review, and submit regulatory documents while maintaining adherence to industry standards.
🔍 Key Responsibilities:
- Prepare and submit regulatory filings for global clinical trials
- Ensure compliance with ICH-GCP, FDA, EMA, and other regulatory guidelines
- Liaise with health authorities, sponsors, and internal teams
- Review and maintain study protocols, informed consent forms (ICFs), and essential documents
- Support inspection readiness and audit processes
✅ Eligibility Criteria
To qualify, candidates should have:
✔ 5+ years of experience in global clinical trial regulatory submissions
✔ Strong knowledge of R&D processes, ICH-GCP, and regulatory guidelines
✔ Excellent communication and project management skills
✔ Experience with eCTD submissions (preferred)
💼 Benefits & Perks
- Competitive salary & performance bonuses
- Flexible & remote work options
- Health & wellness programs
- Continuous learning & development opportunities
- Global exposure in the pharmaceutical industry
📩 How to Apply
Ready to take the next step in your career?
📧 Send your updated CV to:
Ashwini Veerabhadrappa
✉ Email: ashwini.veerabhadrappa@iqvia.com
