✔ Verified by Medical Jobs India
Hiring Junior & Regulatory Affairs Associates
🏢 Parexel (Global CRO)
📍 Remote (Bengaluru)
🎓 Life Sciences / Pharmacy
⏳ 0–4 Years
Parexel is hiring regulatory professionals for Junior and Associate roles in Regulatory Affairs. Strong opportunity to build a career in clinical submissions, regulatory compliance, and global CRO operations.
👉 Learn basics before applying: Clinical Data vs Regulatory Career Guide
📄 Junior Regulatory Affairs Associate (0–2 Years)
Job Overview:
Entry-level role focused on regulatory publishing, document formatting, and submission preparation under global standards.
- Experience: 0–2 Years (Freshers Eligible)
- Qualification: Bachelor’s in Life Sciences / Pharmacy
- Location: Remote (Bengaluru)
- Domain: Regulatory Publishing / Submissions
Key Responsibilities:
- Document formatting, bookmarking & hyperlinking
- Submission compilation and publishing
- File management & document tracking
- Support regulatory submission preparation
- Follow SOPs and submission standards
- Assist in lifecycle management activities
Required Skills:
- Strong attention to detail
- Basic regulatory knowledge
- Team collaboration skills
Salary: ₹3.5 – ₹5.5 LPA
📊 Regulatory Affairs Associate (2–4 Years)
Job Overview:
Mid-level role responsible for handling regulatory submissions, compliance activities, and coordination with global stakeholders.
- Experience: 2–4 Years
- Qualification: Bachelor’s/Master’s in Life Sciences / Pharmacy
- Location: Remote (Bengaluru)
- Domain: Regulatory Affairs / Submissions
Key Responsibilities:
- Manage CTA/iCTA submissions via SUGAM portal
- Handle CTRI registration
- Prepare documents for SEC meetings
- Ensure compliance with NDCT rules
- Track submissions and manage timelines
- Coordinate with sponsors and regulatory teams
Required Skills:
- Hands-on SUGAM & CTRI experience
- Strong regulatory knowledge (India + Global)
- Stakeholder management skills
Salary: ₹6 – ₹10 LPA
🌍 Why Join Parexel?
- Global CRO exposure
- Work on international submissions
- Remote work flexibility
- Strong career growth
- Learning & development opportunities
💡 Interview Tips
- Revise ICH-GCP & NDCT rules
- Understand SUGAM & CTRI workflows
- Prepare submission lifecycle questions
- Focus on documentation accuracy
👉 Practice now: Clinical & Regulatory Quizzes
📄 Resume Tips
- Mention regulatory tools & portals
- Highlight submission experience
- Use keywords: CTA, CTRI, eCTD
- Keep resume concise (1–2 pages)
❓ Frequently Asked Questions
- Freshers eligible? ✔ Yes (Junior role)
- Remote job? ✔ Yes (Bengaluru based)
- Best role? Associate for growth, Junior for entry
🚀 Select Role & Apply
📌 Note: Read the full job description before applying.
📥 How to Apply
- Select your role from dropdown
- Wait for 15-second countdown
- Click Apply button
- Fill application form
- Upload updated resume
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