Description
This position is responsible for the scientific direction for the assigned clinical development programsThis individual has the responsibility for development decisions assessing and integrating the input from various disciplines to create, maintain, and execute a clinical development plan and study design that will result in the regulatory interaction, consultation, filing, and approval of the compound in the therapeutic areaThis individual interacts with internal (e.g., GPT/CST, JPBU, Research, PS, GMS, and other functions at TDC-J/R&D Japan) and external (e.g., KOL, regulatory authority, and patient advocacy group) stakeholders, and influences JPL decision-making by setting strategic and scientific direction and providing expert therapeutic area and clinical development inputLead the clinical development from a viewpoint of science
Create the CDP and LCM plan, lead discussion at JDT, and align with CST (and GPT if...