Senior Medical Writer at Incyte - Regulatory Focus

Elevate your career at Incyte as a Senior Principal Medical Writer focusing on regulatory submissions in Oncology.

Your role includes crafting vital Clinical Study Reports and summaries under strict guidelines.

Incyte is looking for an experienced Principal Medical Writer to produce high-quality regulatory submission documents. You will lead project timelines and collaborate with various stakeholders to meet deadlines. A candidate with eCTD expertise and Oncology knowledge will excel in this position.

Key Responsibilities:

• Develop regulatory documents for global submissions

• Manage writing projects and team communication

• Participate in team meetings focused on deliverables

• Review other relevant project documentation

• Adhere to Incyte's authoring standards and timelines

Requirements:

• Significant experience in regulatory medical writing

• Knowledge of ICH guidelines and eCTD requirements

• Ability to manage projects and collaborate effectively

• Prior experience in Oncology is highly desirable

• Strong writing and organizational skills

Utilize your expertise in regulatory writing to advance Incyte's submissions in the Oncology space.
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