Associate Director Scientific Writing

Role: Associate Director of Scientific Writing within Bristol Myers Squibb's Translational Development, supporting late-stage clinical and translational research in Hematology, Oncology, and Neuroscience. Responsibilities: authoring and reviewing scientific documents such as biomarker reports, regulatory submissions, summaries, and publications; collaborating across functions for data interpretation and document preparation; ensuring timely delivery of reports and supporting regulatory interactions; contributing to scientific communications including abstracts and posters. Requirements: Master’s or PhD in Hematology, Oncology, Neuroscience, with 6-8 years industry or academic experience; strong scientific writing, data interpretation, and regulatory document skills; familiarity with clinical and translational data, late-stage development processes, and global disease strategies. Preferred: experience with IND/NDA submissions, project management, and cross-functional collaboration. High-Value: focus on hematological malignancies, solid tumors, or neuroscience disorders; expertise in clinical, translational, and mechanistic data; supporting late-stage development and regulatory submissions. Work setup: based in NJ, hybrid work model; no specific travel requirements specified.