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Manager of Medical Writing - Remote

Posted 41 weeks ago
Writing
Full Time
Worldwide
$140,000 - $160,000/year

Overview

The Manager of Medical Writing will oversee and lead the development of high-quality scientific documents, including clinical study reports, regulatory submission documents, publications, and other medical communications. This role requires leadership, strategic oversight, and hands-on writing skills. The ideal candidate will collaborate with cross-functional teams, including clinical, regulatory, and medical affairs teams, to ensure the delivery of accurate, clear, and well-structured documents that meet industry standards and regulatory requirements.

In Short

  • Lead a team of medical writers, providing mentorship and training.
  • Develop clinical study reports and regulatory submission documents.
  • Ensure document accuracy and compliance with guidelines.
  • Collaborate with cross-functional teams for document development.
  • Support regulatory submissions and scientific publications.
  • Implement efficient medical writing processes.
  • Review documents for quality and consistency.
  • Provide training for junior writers.
  • Stay updated on industry trends and regulations.
  • Manage multiple projects and meet deadlines.

Requirements

  • Advanced degree in a scientific discipline.
  • 5-7 years of medical writing experience.
  • 2-3 years in a leadership or managerial role.
  • Experience in clinical research and regulatory submissions.
  • Strong knowledge of medical writing standards.
  • Excellent writing and editing skills.
  • Strong project management skills.
  • Ability to collaborate with teams.
  • Attention to detail and commitment to quality.
  • Medical Writing Certification is a plus.

Benefits

  • Competitive salary.
  • Fully remote work environment.
  • Opportunities for professional development.
  • Collaborative team atmosphere.
  • Comprehensive benefits package.

G.R.W.C

Global Regulatory Writing & Consulting

Global Regulatory Writing & Consulting is a leading organization specializing in medical writing and regulatory consulting services within the pharmaceutical, biotechnology, and healthcare industries. The company is dedicated to ensuring the highest standards of quality, scientific rigor, and regulatory compliance in all medical writing deliverables. With a focus on strategic direction and process improvements, Global Regulatory Writing & Consulting collaborates closely with clinical development, regulatory affairs, and other stakeholders to support successful clinical and regulatory goals. The company fosters a high-performance culture, emphasizing professional development and expertise in medical writing, while maintaining a commitment to excellence in scientific communication and regulatory submissions.

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