Join Precision Medicine Group as a Senior Medical Writer and drive clinical documentation excellence. Your regulatory expertise will be crucial in producing high-quality clinical documents.
This role requires a skilled professional with more than 5 years of experience in medical writing, particularly within CRO or sponsor environments. You will be responsible for enhancing the quality and efficiency of study documents while collaborating effectively with various teams to meet demanding project timelines.
Key Responsibilities:
• Write and produce clinical documents per regulatory guidelines
• Ensure efficient management of the document lifecycle
• Transform clinical data into clear written content
• Improve and maintain medical writing procedures
• Research to substantiate writing claims
Requirements:
• BS degree in a relevant scientific discipline
• 5+ years of medical writing experience in CRO/sponsor settings
• Proficient in Microsoft and Adobe applic...