Sr.Director/Director, Clinical Scientist

Provide scientific expertise throughout the lifecycle of a drug product by developing and implementing clinical protocols. You would review, evaluate, and present study data while contributing to clinical study reports, investigator brochures, regulatory documents, and publications. You will also work collaboratively to ensure the integrity of Neumora-sponsored clinical trials and that data is collected in compliance with protocols and guidelines. Responsibilities include creating and maintaining key strategic documents such as clinical development plans and protocols, as well as contributing to the development of clinical sections of regulatory documents. You will analyze and interpret study data, ensuring ethical and safety standards, and develop relationships with key investigators to optimize scientific quality. You'll also support clinical trial start-up and execution, write abstracts, and contribute to therapeutic area research.