📑 Associate – Regulatory Affairs (Publishing) | Freshers
ClinChoice
Chennai
0–1 Year
Regulatory Affairs
eCTD Publishing
Office-Based
🏢 About ClinChoice
Founded in 1995, ClinChoice is a global CRO providing expertise in clinical operations, biometrics, regulatory affairs, pharmacovigilance, medical affairs, and toxicology.
The company supports pharmaceutical, medical device, and consumer healthcare companies worldwide in accelerating clinical trials and regulatory approvals.
📌 Job Overview
Position: Associate – Regulatory Affairs (Publishing)
Location: Chennai, India
Work Model: Office-based
Experience: 0–1 Year (Freshers Eligible)
Employment Type: Contract
Industry: Regulatory Affairs / eCTD Publishing
🧾 Key Responsibilities
- Support preparation of eCTD & non-eCTD submissions
- Document formatting, bookmarking & PDF optimization
- Assist in submission compilation & publishing
- Perform technical validation checks
- Maintain submission trackers & logs
- Ensure metadata accuracy & document placement
- Support lifecycle management activities
- Ensure compliance with USFDA, EMA & global standards
🎓 Qualifications & Skills
- Bachelor’s degree in Life Sciences / Pharmacy / Biotechnology
- Freshers & 0–1 year experience eligible
- Basic understanding of regulatory environment
- MS Office proficiency
- Knowledge of eCTD publishing concepts
- Familiarity with Veeva Vault, Lorenz DocuBridge (preferred)
- High attention to detail
- Strong communication skills
💼 Why Start Your Regulatory Career Here?
- Entry-level opportunity in Regulatory Affairs Publishing
- Hands-on exposure to eCTD lifecycle management
- Work with global health authority requirements
- Career path toward Regulatory Affairs Specialist roles
- Strong learning & global CRO environment
💰 Expected Salary
₹2.8 – ₹4.2 LPA (Entry-level RA Publishing roles in Chennai)
📌 Note Before You Apply:
Read the job responsibilities carefully. Ensure your understanding of regulatory submissions, document formatting, and publishing workflows aligns with the role.
Read the job responsibilities carefully. Ensure your understanding of regulatory submissions, document formatting, and publishing workflows aligns with the role.
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