Sign up to access all features of our service.
  • Job search
  • Favorites
  • Create a CV
    New
  • Salaries
  • Subscriptions

Senior Principal Medical Writer at Incyte

Syneos Health

Elevate your career with Incyte as a Senior Principal Regulatory Medical Writer specializing in Oncology. Lead document development for regulatory submissions while ensuring ICH compliance and adherence to project timelines. Incyte seeks a skilled Regulatory Medical Writer to facilitate oncology-focused document creation and management. You will spearhead the development of critical materials such as Clinical Study Reports and contribute in cross-functional meetings to align project goals and ensure timely deliverables. Your expertise will directly impact adherence to corporate standards in regulatory documentation. Key Responsibilities:

  • Develop global regulatory submission documents
  • Oversee project timelines and team communication
  • Provide input in cross-functional meetings for deliverables
  • Review documents for regulatory compliance
  • eCTD submission experience is advantageous
Requirements:
  • In-depth knowledge of regulatory writing and ICH standards
  • Strong organizational and project management skills
  • Excellent communication and collaboration capabilities
  • Experience with clinical documentation processes
  • Ability to meet tight deadlines and objectives
Utilize your oncology expertise to advance regulatory documentation at Incyte. #J-18808-Ljbffr

Vacancy posted more than 2 months ago

Do you want to receive more vacancies?

Subscribe and receive similar vacancies to Senior Principal Medical Writer at Incyte. Be the first to apply!