Lead Medical Writer - Regulatory Submissions & Docs

Lead Medical Writer - Regulatory Submissions & Docs

Full-Time 55000 - 77000 Β£ / year (est.) No working from home possible
Job Search Place Limited

At a Glance

  • Tasks: Lead the creation of regulatory and clinical documents for international submissions.
  • Company: Job Search Place Limited, a leader in medical writing.
  • Benefits: Competitive salary, flexible working hours, and opportunities for professional growth.
  • Other info: Join a dynamic team dedicated to excellence in healthcare documentation.
  • Why this job: Make a significant impact in the medical field by ensuring compliance and quality.
  • Qualifications: 5+ years of medical writing experience and strong coordination skills.

The predicted salary is between 55000 - 77000 Β£ per year.

Job Search Place Limited is looking for a Principal Medical Writer in Kiveton Park, England. This role involves leading the development of regulatory and clinical documents and requires at least 5 years of experience in medical writing, particularly with international submissions.

The ideal candidate will:

  • Guide document preparation
  • Coordinate with cross-functional teams
  • Ensure compliance with regulatory standards

Lead Medical Writer - Regulatory Submissions & Docs employer: Job Search Place Limited

Job Search Place Limited is an exceptional employer that values innovation and collaboration in the heart of Kiveton Park, England. With a strong commitment to employee development, we offer comprehensive training programmes and opportunities for career advancement, fostering a supportive work culture where your contributions are recognised and rewarded. Join us to be part of a dynamic team dedicated to making a meaningful impact in the field of medical writing.

Job Search Place Limited

Contact Details:

Job Search Place Limited Recruitment Team

We think you need these skills to ace Lead Medical Writer - Regulatory Submissions & Docs

Medical Writing
Regulatory Submissions
Clinical Document Development
Cross-Functional Team Coordination
Regulatory Compliance
Document Preparation
Experience in International Submissions