Director, Clinical Medical Writing

vaxcyte · San Carlos, California, United States

Posted
60 days ago
Last confirmed live
2 days ago

What this role involves

Vaxcyte seeks a Director, Clinical Medical Writing to lead medical writing activities, manage contract writers, and generate clinical regulatory documents. The role involves developing SOPs, templates, and ensuring high-quality deliverables for clinical trials. The successful candidate will collaborate cross-functionally and provide strategic guidance on medical writing best practices.

Skills this posting asks for

  • medical writing
  • regulatory documentation
  • clinical protocol development
  • investigator brochure
  • informed consent
  • clinical study reports
  • sop development
  • veeva vault
  • vendor management
  • budgeting
  • cross-functional collaboration
  • quality assurance
  • document management
  • template development
  • project management
  • strategic planning
  • leadership
  • communication
  • clinical trials
  • ind submission
  • manuscript writing
  • pharmacy manual
  • listing review
  • data quality

Requirements

  • Level: director

From the employer’s posting

Join our Mission to Protect Humankind! Vaxcyte is a clinical-stage vaccine innovation company engineering high-fidelity vaccines to protect humankind from the consequences of bacterial diseases, which have serious and costly health consequen…

Read the full description on vaxcyte’s careers page

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