Senior Medical Writer at Precision Medicine

Join Precision Medicine Group as a Senior Medical Writer and shape clinical documentation with your regulatory expertise. Utilize your extensive writing background to enhance study quality and compliance across various projects.

In this senior role, you will leverage your 5+ years of medical writing experience within CRO or sponsor settings. You'll be responsible for producing and editing high-quality clinical documents that adhere to ICH and FDA standards. Engage in proactive communication with teams while ensuring documents meet regulatory requirements and deadlines.

Key Responsibilities:

• Write and edit clinical documents for regulatory compliance

• Plan and produce documents following guidelines

• Oversee the document lifecycle process

• Distill clinical data into clear written content

• Enhance medical writing processes and quality

Requirements:

• BS degree in a relevant scientific field

• 5+ years in medical writing at CRO/sponsor

• Proficiency in Microsoft and Adobe software

• Strong knowledge of ICH, FDA, and GCP

• Exceptional attention to detail and deadlines

Drive impactful clinical studies and leverage your medical writing skills at Precision Medicine.
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