Advise on clinical development strategy, program priorities, and development plans across• the company's portfolio Provide input on clinical trial design, including study objectives, endpoints, patient• populations, dose selection, and overall development approach Advise on clinical, regulatory, and operational considerations relevant to development,• including first-in-human and early-phase clinical studies Review and provide strategic input on scientific data and clinical development materials,• including clinical development plans, protocols, investigator materials, and regulatory• documents Advise on the selection, oversight, and engagement of clinical development partners and• CROs Participate in meetings with company leadership, regulatory authorities, clinical• investigators, and external development partners, as requested Work with internal teams to integrate nonclinical, translational, CMC, and regulatory• considerations into clinical development planning Provide additional strategic clinical development advice and subject-matter expertise as• reasonably requested by the company Work closely with scientists and operators in a fast-paced biotech startup environment,• operating effectively with a high degree of autonomy. MD, PhD, PharmD, or equivalent advanced degree in a relevant scientific or medical field,• with 15+ years of relevant industry experience in clinical development preferred Proven track record of developing and executing clinical development strategies, from IND• through early- and later-stage clinical trials Experience designing clinical trials, including selection of endpoints, patient populations, and• dosing strategies Experience developing biologics, including antibody or antibody-conjugate programs,• strongly preferred Experience selecting and managing clinical CROs and other external development partners.