Medical Writer

Responsibilities :

• Prepare and review clinical documents for regulatory submissions.
• Perform quality checks on clinical documents.
• Initiate and conduct start-up meetings related to the development of clinical documents.
• Collaborate with study teams to ensure effective document development.
• Manage project timelines for document development.
• Ensure all clinical documents adhere to Standard Operating Procedures, Document Standards, and Guidance documents.
• Review statistical analysis plans and associated tables, figures, and listings as required.

Desired Skills :

• Proficiency in Medical Writing and Protocol development.

Qualifications :

• Bachelor of Pharmacy (B.Pharm)
• Master of Pharmacy (M.Pharm)

Skills Required

Clinical Research, Medical Terminology, Data Analysis, literature review