Associate Director of Scientific Writing

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