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Hiring Regulatory Affairs Associate (Clinical Trial Application)
🏢 Parexel
🌐 Remote (India)
🎓 Pharmacy / Life Sciences
📄 Regulatory Affairs
Parexel is hiring Regulatory Affairs Associate for clinical trial submissions, SUGAM portal, and NDCT regulatory processes.
👉 Learn Regulatory Affairs career: B.Pharm Career Guide
📘 Understand clinical research: Clinical Research Guide
📋 Job Overview
- Role: Regulatory Affairs Associate (CTA)
- Company: Parexel
- Location: Remote (India)
- Experience: 2–4 Years
- Qualification: Pharmacy / Life Sciences
- Job Type: Full-Time
- Salary: ₹5 – ₹10 LPA
📌 Key Responsibilities
- Prepare Clinical Trial Applications (CTA/iCTA)
- Submit via SUGAM portal
- Manage amendments and query responses
- Handle CTRI registrations
- Support SEC meeting documentation
- Track NDCT Rules and regulatory updates
- Maintain submission timelines
- Ensure compliance with Indian & global regulations
- Coordinate with sponsors and teams
📊 Learn systems: Clinical Data vs SAS
🎯 Required Skills
- SUGAM portal submissions
- NDCT Rules knowledge
- CTRI registration
- Regulatory documentation
- Communication & stakeholder management
🧠 Practice interview: Interview Prep
🎓 Eligibility
- B.Pharm / M.Pharm / Life Sciences
- 2–4 years Regulatory Affairs experience
- Clinical trial submission experience required
- Global regulatory exposure preferred
💰 Salary & Benefits
- ₹5 – ₹10 LPA
- Remote work flexibility
- Global CRO exposure
- Career growth in regulatory affairs
🚀 Job Application Link
📌 Important Note Before You Apply:
Kindly read the complete job description carefully before applying. Ensure your experience matches SUGAM, NDCT, and CTA submissions requirements before proceeding.
Kindly read the complete job description carefully before applying. Ensure your experience matches SUGAM, NDCT, and CTA submissions requirements before proceeding.
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