Principal Med Writer

📋 Description

• Research, write, edit, and develop clinical study reports, clinical study protocols, and scientific
• Serve as the primary author and provide expert input on complex clinical, scientific, and
• Conduct senior-level reviews of routine and complex documents, ensuring scientific accuracy
• Advise project teams and clients on document development strategies, applicable regulatory
• Provide training, guidance, and mentorship to medical writers and program managers on document
• Develop, review, and promote best practices, methods, and techniques that improve the quality and

🎯 Requirements

• A relevant academic background in life sciences, medicine, pharmacy, biomedical sciences, or
• Demonstrated experience in medical and scientific writing, including the preparation, editing, and
• Strong familiarity with regulatory submission documents, including IBs, INDs, and MAAs, as well as
• Ability to interpret clinical study data, synthesize complex scientific information, and
• Excellent writing, editing, proofreading, and document-review capabilities, with strong attention
• Proven ability to provide technical guidance, train junior colleagues, review team deliverables

🎁 Benefits

• Fully remote work from India.
• Full-time employment with a standard Monday-to-Friday work schedule.
• Opportunities to deepen medical writing expertise and expand knowledge of clinical research and
• Senior role involving document ownership, technical review, mentoring, and guidance.
• Contribute to clinical development programs through high-quality scientific documents.
• Work with multidisciplinary teams and internal/external stakeholders.