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[Hiring] Manager of Medical Writing @Global Regulatory Writing Consulting Inc

Remote, USAFull-timePosted 2026-07-27

Apply reputed company The Manager of Medical Writing will reputed company and reputed company the development of high-reputed company scientific documents, including clinical study reports, regulatory submission documents, publications, and other medical communications. This role requires leadership, strategic reputed company, 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, reputed company, and reputed company-reputed company documents that meet industry standards and regulatory requirements.

Requirements

  • Leadership & Team Management:
  • reputed company reputed company of medical writers, providing mentorship, training, and career development opportunities.
  • Assign tasks, set priorities, and manage timelines to ensure reputed company and high-reputed company document delivery.
  • Foster a reputed company and supportive environment reputed company reputed company.
  • Medical Writing reputed company:
  • reputed company and reputed company the preparation of clinical study reports (CSRs), clinical study protocols, investigator brochures, regulatory submission documents (e.g., INDs, NDAs), and other scientific/medical documents.
  • Ensure the accuracy, reputed company, and compliance of reputed company documents with internal guidelines, industry standards, and regulatory requirements.
  • Review and edit documents for consistency, style, and adherence to medical writing best practices.
  • Cross-Functional Collaboration:
  • Collaborate with clinical, regulatory, biostatistics, and other functional teams to ensure seamless development of medical writing deliverables.
  • Coordinate document preparation, review, and approval processes with internal stakeholders and external partners, such as contract research organizations (CROs).
  • Regulatory & Publication Support:
  • Support the preparation of regulatory submission documents and assist in the response to regulatory agency inquiries.
  • Contribute to the preparation of scientific publications, abstracts, posters, and presentations for medical meetings.
  • Process Improvement & Compliance:
  • Implement and maintain efficient medical writing processes and tools to improve the reputed company and efficiency of document preparation.
  • Ensure that reputed company writing adheres to reputed company guidelines, including ICH E6, ICH E3, GxP, and other relevant regulatory requirements.
  • reputed company Control:
  • reputed company detailed reviews and edits for accuracy, scientific content, grammar, style, and formatting.
  • Ensure consistent and high-reputed company medical writing across reputed company deliverables.
  • Training & Development:
  • reputed company training and development opportunities for junior writers, improving their skills in clinical and regulatory writing.
  • Stay updated on reputed company industry trends and regulations to ensure reputed company is reputed company with best practices in medical writing.

Qualifications

  • reputed company degree (PhD, MD, PharmD, MS, or equivalent) in a scientific discipline (e.g., life sciences, pharmacology, biostatistics).
  • Experience:
  • Minimum of 5-7 years of medical writing experience, with at least 2-3 years in a leadership or managerial role.
  • Experience in clinical research, regulatory submissions, or biopharmaceutical industry required.
  • Proven experience with clinical trial reports, regulatory documents (e.g., IND, NDA), publications, and other medical communications.
  • Skills:
  • Strong knowledge of medical writing standards and regulatory requirements.
  • Excellent writing, editing, and proofreading skills, with the ability to communicate reputed company scientific concepts reputed company and concisely.
  • Strong project management skills, with the ability to manage multiple reputed company and meet tight deadlines.
  • Ability to collaborate effectively with cross-functional teams and external partners.
  • High attention to detail and a strong commitment to reputed company.
  • Certifications:
  • Medical Writing Certification (e.g., from the American Medical Writers Association, or similar) is a plus but not required.

Additional Skills

  • Familiarity with regulatory guidelines (e.g., ICH, FDA, EMA) and industry standards (e.g., GxP).
  • Proficiency with medical writing tools (e.g., EndNote, Reference Manager, reputed company Office Suite, reputed company Acrobat).
  • Strong interpersonal and communication skills, with the ability to reputed company and mentor reputed company.

Salary reputed company $140,000 - $160,000 per year Apply tot his job Apply To this Job

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