✔ 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
Junior Regulatory Affairs Associate link expired
🚀 Job Application Links (Parexel)
📌 Important Note Before You Apply:
Kindly read the full job description carefully for your selected role before applying. Ensure your profile aligns with regulatory affairs submissions, global compliance standards, dossier maintenance, and life sciences documentation workflows before submitting your details.
Kindly read the full job description carefully for your selected role before applying. Ensure your profile aligns with regulatory affairs submissions, global compliance standards, dossier maintenance, and life sciences documentation workflows before submitting your details.
📥 How to Apply
- Read the full job description thoroughly for your desired role
- Click on the specific Apply Now button above
- Fill out the application form on the official Parexel portal carefully
- Upload your updated resume or CV
- Submit your application
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