Clinical Scientist 2, Clinical Development

Responsibilities Provide scientific leadership and independent contribution to study design, protocol development, and clinical development planning Support the development, implementation, conduct, oversight, and reporting of clinical trials Perform comprehensive literature reviews and maintain current knowledge of relevant disease areas Participate in the review and interpretation of clinical data Collaborate cross-functionally with Clinical Operations, Data Management, etc. Draft and contribute to clinical and regulatory documents Support or lead scientific interactions with CROs, investigators, and external collaborators Develop and maintain productive relationships with external scientific experts Requirements MSc or PhD degree in Life Sciences, Biomedical Sciences, Pharmacology or related scientific discipline 2-5 years of post-doctoral experience and/or relevant industry experience, preferably in neurosciences Experience in clinical research and clinical development with strong understanding of study design and clinical data review Experience drafting, reviewing, or supporting clinical and regulatory documentation Working knowledge of GCP, ICH guidelines, and familiarity with FDA and EMA environments Strong written, verbal, interpersonal, and presentation skills Strong organizational skills and attention to detail Experience in neuroscience, CNS, psychiatry, neurology, or related therapeutic areas is preferred Experience working with investigators, CROs, vendors, and external scientific experts is preferred. #J-18808-Ljbffr Jobtailor