Associate - Regulatory Affairs (Publishing) at ClinChoice

📋 Description

• Support preparation of eCTD and non-eCTD submissions.
• Format documents, hyperlink, bookmark, and optimize PDFs.
• Assist in submission compilation and publishing.
• Conduct technical validation checks prior to submission.
• Maintain submission trackers and documentation logs.
• Ensure metadata accuracy and correct document placement.

🎯 Requirements

• Bachelor’s degree (Life Sciences / Pharmacy / Biotechnology preferred).
• 0–1 year experience (freshers may apply).
• Basic understanding of pharmaceutical regulatory environment.
• Good knowledge of MS Office (Word, Excel, PowerPoint).
• Strong attention to detail.
• Familiarity with publishing tools (eCTD tools, Veeva Vault, Lorenz DocuBridge).
• Time management and ability to meet deadlines.