Senior Medical Writer at ProPharma

Enhance patient care as a Senior Medical Writer with Pro Pharma, supporting a leading Pharmaceutical client. Focus on authoring clinical and regulatory documents with quality and efficiency.

Join Pro Pharma, a trusted partner for biotech, med device, and pharmaceutical organizations. Seeking an experienced Senior Medical Writer with at least seven years of early phase experience. You'll manage complex documents, coordinate resources, and ensure compliance with regulatory standards, directly impacting scientific breakthroughs and new therapies.

Key Responsibilities:

• Author and edit clinical and regulatory documents

• Manage clinical program documents for assigned clients

• Coordinate resources for medical writing and quality control

• Supervise and mentor junior medical writers

• Ensure document compliance with established guidelines

Requirements:

• Bachelor’s degree in a medical or scientific discipline

• Minimum of 7 years writing clinical regulatory documents

• Advanced knowledge of FDA regulations and guidelines

• Proficient in MS Word and project management

• Strong communication skills and attention to detail

Become part of a dedicated team, impacting healthcare by delivering high-quality medical writing solutions.
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