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Erasca is a clinical-stage precision oncology company focused on discovering, developing and commercializing medicines for the benefit of patients with cancer. Our programs take novel approaches to shutting down one of cancer’s  most commonly mutated signaling cascades, the RAS/MAPK pathway, which affects approximately 5.5 million lives each year worldwide. The name “Erasca” has an important embedded meaning: it is a contraction of our audacious hope to “erase cancer” that drives our mission and everything that we do on behalf of patients with cancer. Position Summary:     Reporting to the  Chief Medical Officer, the Senior or Executive Director, Clinical Development will  drive the clinical aspects of late-stage clinical development studies or programs.  This person will work closely with cross-functional teams in the management and execution of the  Clinical Development Plan (CDP), in developing innovative and efficient solutions to medical and scientific clinical trial issues, and  in  ensuring the successful execution and completion of clinical trials.  T he Senior  or Executive  Director, Clinical  Science will  also  have individual study level responsibility  for one or more trials .   Essential Duties and Responsibilities:    Lead in the planning and execution of clinical studies to successfully move the program through pivotal trials and eventual submission, regulatory approval, and launch .   Key clinical deliverables include document development (INDs, Protocols, IBs, applicable regulatory documents, etc.), medical and scientific input into the development of deliverables required for study activation and study conduct (CRFs, SAP, data listings, etc.), data review, and other deliverables as needed.   May a ttend and contribute  at  meetings with Health Authorities (HAs) related to program; develop  responses to HAs and IRBs on clinical/medical questions.   Represent Erasca externally at scientific meetings and congresses.   Establish and  maintain  strong relationships with internal teams, clinical investigators, regulatory agencies, and key stakeholders.   Gather,  analyze  and interpret clinical data,  providing  strategic insights to inform critical decisions and guide program development.   Manage clinical development timelines effectively, ensuring efficient resource allocation and achievement of milestones.   Perform all duties in keeping with the Company’s core values,  policies,  and all applicable regulations.   Required Education and Experience:   Undergraduate degree  required ;   PhD, PharmD, or other relevant advanced degree in a health science field  highly preferred.   At least  10  years of biotech or pharmaceutical industry experience as a clinical scientist or in a  closely  related clinical development function.   E xtensive experience i n oncology clinical trials  required ;   late-stage  development experience  required ,  early development  experien ce  a plus .   Experience leading clinical development contributions to regulatory submissions (e. g. ( NDA, PIP/PSP, label negotiation, Breakthrough Therapy Designation, Accelerated Review) highly preferred .   E xperience in dynamic  start  up or small company environment s   required .   Demonstrated ability to contribute to strategic clinical planning and work effectively independently and on cross-functional teams.   Demonstrated ability to evaluate, interpret, and present compl