🚨 Regulatory Affairs Officer
- 🏢 Company: IQVIA
- 📍 Location: Bangalore, India
- 🎓 Eligibility: Bachelor’s or Master’s in Pharmacy, Life Sciences, or related fields
- 🧪 Experience: 2+ Years
- 📝 Job Type: Full-Time | Regulatory Affairs
- 🔎 Verified: ✅ Verified Opportunity
🧬 About Company
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.
📄 Job Overview
Job Title: Regulatory Affairs Officer
Job ID: R1495142
Location: Bangalore, India
Last Date to Apply: July 28, 2025
🧑💼 Key Responsibilities
- 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).
- Track project timelines and manage workload effectively.
- Participate in client meetings and assist in business development activities.
✅ Required Skills & Qualifications
- Bachelor’s or Master’s degree in Pharmacy, Life Sciences, or related field.
- Minimum 2 years in regulatory affairs (CMC, submissions, lifecycle management).
- Proficiency in Microsoft Office & regulatory publishing tools.
- Excellent communication & organizational skills.
🎯 Benefits at IQVIA
- 🌎 Global exposure to pharma & biotech clients.
- 📈 Career growth & professional development programs.
- 💼 Structured work policies for work-life balance.
- 🧪 Opportunity to contribute to innovative drug development projects.
🔗 Apply Link (Opens After 15 Seconds)
📌 Note Before You Apply:
We use a 15-second timer to encourage you to read the job description carefully before applying. Understanding the role increases your chances of success and helps create a strong impression.
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