Associate Director of Scientific Writing

Job Summary

Reporting to the Program Management Lead, the full-time Associate Director of Scientific Writing will be responsible for writing and managing scientific documents, including regulatory submissions and publications, while collaborating with Translational scientists in a hybrid work environment.

Key responsibilities

• Ensure timely delivery of pre-clinical and translational biomarker reports across various disease areas
• Establish annual publication goals and plans in conjunction with Translational Development scientists, ensuring deadlines for regulatory submissions are met
• Collaborate with cross-functional teams to execute scientific communications and regulatory documents effectively

Required qualifications

• Masters or PhD in Hematology, Oncology, Neuroscience, or a related field with 6-8 years of relevant experience
• Proven experience with regulatory submissions such as IND and NDA/sNDA
• Strong background in writing scientific documents and developing communication strategies
• Ability to interpret complex data and present it clearly in narrative formats
• Experience managing scientific collaborations and projects across multiple functions