✍️Regulatory Writer Job Opportunity

We are seeking experienced Regulatory Writers to author key clinical documents, including Clinical Study Reports (CSRs), protocols, Investigator Brochures (IBs), and CTD summaries. The successful candidate will have a strong scientific background and experience in writing regulatory documents for pharmaceutical companies.

💼Job Details:

Location: Bangalore, Hyderabad, Mumbai, Pune, Delhi NCR

Mode of Work: Hybrid (2 days WFO)

Level: Associate, Sr Associate, Associate-Manager

Experience: 3-15 years

🧾Key Responsibilities:

Author key clinical documents, including CSRs, protocols, IBs, and CTD summaries and other regulatory documents

Ensure compliance with global regulatory requirements

Collaborate with cross-functional teams to plan, develop, and finalise documents

Manage timelines and ensure consistency across documents

Work independently or as part of a therapeutic area team

🎓Requirements:

Strong scientific knowledge and experience in writing regulatory documents

Proficiency in MS Word, document management systems, and structured content tools

Ability to manage timelines and work independently

Excellent communication and collaboration skills

🌟What We Offer:

Competitive salary and benefits package

Opportunity to work with a leading company in the pharmaceutical industry

Collaborative and dynamic work environment

📩 How to Apply

If you are a motivated and detail-oriented Regulatory Writer passionate about creating high-quality clinical documents, send your updated resume to:
📧 mdasetti@primusglobal.com