Job Description
Advance your career as a Regulatory Medical Writer with a focus on Oncology at Incyte. Lead the development of regulatory documents for submissions adhering to ICH and corporate standards.
Incyte is hiring a Senior Principal Regulatory Medical Writer to facilitate the creation and management of critical documents like Clinical Study Reports. You'll ensure adherence to timelines while collaborating with various teams across the organization. Your participation in cross-functional meetings will guide the medical writing process to meet overall project goals.
Key Responsibilities: • Develop global regulatory submission documents • Oversee project timelines and facilitate team communication • Provide input in cross-functional meetings for deliverables • Review project-related documents for compliance • eCTD submission experience is a bonus
Requirements: • In-depth knowledge of regulatory writing and ICH compliance • Strong organizational and project management ca...
Incyte is hiring a Senior Principal Regulatory Medical Writer to facilitate the creation and management of critical documents like Clinical Study Reports. You'll ensure adherence to timelines while collaborating with various teams across the organization. Your participation in cross-functional meetings will guide the medical writing process to meet overall project goals.
Key Responsibilities: • Develop global regulatory submission documents • Oversee project timelines and facilitate team communication • Provide input in cross-functional meetings for deliverables • Review project-related documents for compliance • eCTD submission experience is a bonus
Requirements: • In-depth knowledge of regulatory writing and ICH compliance • Strong organizational and project management ca...