Principal Medical Writer

About the role

To author and review regulatory & other medical writing deliverables independently as per high-quality standards (internal & external) and within expected timelines. Support in building technical & functional expertise within the group by designing & executing robust training programs. Contribute/support other writers for manuscripts, slide sets, abstracts, posters, other techno-commercial documents as needed.

What you'll do

• Position will have management responsibilities
• Support in building technical & functional expertise within the group by designing & executing robust training programs
• Contribute/support other writers for manuscripts, slide sets, abstracts, posters, other techno-commercial documents as needed
• Work with data analysts and statisticians on Real world and other evidence generation projects
• Follow all internal and client processes and adhere to various ICH / regulatory guidelines and other industry best practices

What you need

• 10–11 yrs of experience
• Clinical research
• Performance management
• Communication
• Quality control
• SOP writing
• Documentation
• M.Pharm or PhD