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Director of Medical Writing - Remote

Posted 25 weeks ago
All others
Full Time
Worldwide

Overview

The Director of Medical Writing is a senior leadership role responsible for overseeing the strategic direction, management, and execution of medical writing activities across clinical, regulatory, and publication-related projects. This position will play a critical role in ensuring that all medical writing deliverables meet the highest standards of quality, scientific rigor, and regulatory compliance. The Director will lead a team of medical writers, collaborate with key stakeholders, and drive process improvements, all while contributing to the success of the company’s clinical and regulatory goals. 

In Short

  • Oversee medical writing activities across clinical, regulatory, and publication projects.
  • Lead and mentor a team of medical writers.
  • Ensure compliance with regulatory guidelines and industry standards.
  • Collaborate with cross-functional teams for high-quality document delivery.
  • Define best practices for medical writing processes.
  • Manage the department’s budget and resources.
  • Provide training and development for medical writing staff.
  • Oversee preparation of scientific and regulatory documents.
  • Maintain knowledge of evolving regulatory requirements.
  • Support the preparation of regulatory submissions.

Requirements

  • Advanced degree in a scientific discipline required.
  • 8-10 years of medical writing experience in relevant industries.
  • 5 years in a leadership or senior management role.
  • Strong leadership and team management skills.
  • Excellent written and verbal communication skills.
  • Strong project management skills.
  • Advanced knowledge of medical writing tools.
  • Certification in Medical Writing is desirable.
  • Understanding of clinical trial design and data interpretation.
  • Ability to manage high-pressure situations.

Benefits

  • Competitive salary and benefits package.
  • Opportunity for professional development and growth.
  • Work in a dynamic and collaborative environment.
  • Flexible working hours.
  • Fully remote work option.

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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