Senior Medical Writer

ProPharma

**
High-quality medical writing deliverables
Adherence to regulatory standards and guidelines
Client expectation management
** ProPharma is seeking a Senior Medical Writer with a minimum of 5 years of experience in clinical and regulatory document writing for the biotech, pharmaceutical, or medical device sectors. The role involves creating high-quality medical writing deliverables and mentoring junior writers, all while adhering to regulatory standards and managing client expectations. **

Job Summary

  • With minimal supervision, authors high-quality medical writing deliverables across all phases of clinical research and in various therapeutic areas.
  • Manages client expectations, interacts directly with clients, leads team meetings, and manages deliverable timelines.
  • ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle.

Matching Summary

Match Score: 75

** ProPharma is seeking a Senior Medical Writer with a minimum of 5 years of experience in clinical and regulatory document writing for the biotech, pharmaceutical, or medical device sectors. The role involves creating high-quality medical writing deliverables and mentoring junior writers, all while adhering to regulatory standards and managing client expectations. **

Skills & Requirements

Must-have

  • High-quality medical writing deliverables
  • Adherence to regulatory standards and guidelines
  • Client expectation management
  • Collaboration with subject matter experts
  • Proficiency in MS Word
  • Exceptional project management skills

Nice-to-have

  • Growth mindset and positive outlook
  • Proactive initiative and new challenges
  • Innovative, collaborative, and entrepreneurial spirits
  • Authentic self in the workplace

Key Requirements

  • Minimum 5 years experience
  • Bachelor's degree or higher
  • Experience in clinical and/or regulatory documents

Work Rights

Not specified

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