Executive Director, Global Medical Affairs, Lung - Palo Alto

The Executive Director of Medical Affairs for Lung is a key leader and expert in lung cancer responsible for shaping and executing the medical affairs strategy. · ...

The Executive Director, Medical Affairs, Lung is a key leader and subject matter expert responsible for shaping and executing the medical affairs strategy in lung cancer. · ...

The Executive Director, Medical Affairs, GI is a key leader and a subject matter expert responsible for shaping and executing the medical affairs strategy in GI cancers. · Strategic Leadership Develop and lead the US medical affairs strategy for GI cancers. · Foster a culture of ...

We are currently seeking a Regulatory Affairs Strategy Intern. This is a paid, full-time time position for the Summer 2025. · The candidate will work closely with and report to the Regulatory Affairs Leadership team and will gain experience in the RA life cycle process. · The pay ...

This is an onsite role based in Palo Alto, CA, · The Senior Manager, Medical Education & Grants (SM) is responsible for helping build, execute, · and optimize Summit's independent and continuous medical education programs (IME/CME) · in alignment with the company's scientific and ...

About Summit is a biopharmaceutical oncology company with a mission focused on improving quality of life increasing potential duration of life and resolving serious unmet medical needs At Summit we believe in building a team of world class professionals who are passionate about t ...

The Executive Director Global Medical Affairs GI oversees medical affairs plans for lung-related indications including launch excellence lifecycle management scientific engagement. Recent hands-on experience in GI cancers either clinical practice pharmaceutical companies required ...

The Director, Medical Information (MI) is a strategic leader responsible for building, scaling, and overseeing the MI function to ensure launch readiness and ongoing scientific excellence. · Lead and implement the design and build-out of the MI infrastructure (i.e., MI Call Cente ...

The Principal Statistical Analyst will support and/or lead statistical programming activities for clinical trial data collection analysis reporting visualization on all Summit drugs. · ...

The company is a biopharmaceutical organization situated in the San Francisco Bay Area. They specialize in antibody discovery and engineering. · Dynamic and experienced Sr Manager / Associate Director of Regulatory Affairs responsible for ensuring the execution of regional regula ...

We are seeking an adaptable future-thinking and decisive leader who is solidly grounded in clinical development to provide strategic leadership across DELFI's clinical study portfolio working closely with executive leadership and cross-functional teams including R&D medical quali ...

The VP, · Clinical Development and Trial · Innovation provides strategic leadership across DELFI's clinical study portfolio, · working closely with executive leadership and cross-functional teams including R&D, · medical, quality, and regulatory.This leader defines and shapes the ...

The Director of Statistical Programming oversees managing statistical programming projects and creating strategic plans related to clinical trials and medical affairs publications.PhD with 8+ years of experience or MS with 11+ years of experience in statistics or biostatistics or ...

+ Job summary: We are seeking a physician to serve as a Medical Director to oversee global Phase 3 clinical trials and BLA filings. The incumbent will be primarily responsible for developing and executing integrated clinical trial programs including protocol design and medical ov ...

The company is seeking an experienced and driven Medical Director to lead and support the clinical development of their oncology pipeline programs from Phase1-Phase 3. · Provide strategic input into the design and execution of oncology clinical development plans and clinical tria ...

The Vice President of Program Management reports to the Chief Business & Strategy Officer and leads the cross-functional program management team to maximize the value of Summit's pipeline drug candidates. · ...

Job summary · Gain hands-on experience in Regulatory Affairs while working with energetic colleagues and inspirational leaders. · Work closely with the Regulatory Affairs Leadership team. · ...

The Senior Manager, Medical Education & Grants (SM) is responsible for helping build execute and optimize Summit's independent and continuous medical education programs (IME/CME) in alignment with the company's scientific and medical strategy. · Assist in building and implementin ...

Job Summary · About Summit · Summit Therapeutics Inc. is a biopharmaceutical oncology company with a mission focused on improving quality of life, increasing potential duration of life and resolving serious unmet medical needs. · Total compensation package for this position may a ...

The Associate Director, Global Data Generation will play a critical role in driving the strategy, planning and execution of data generation initiatives to support development and commercialization. · The ideal candidate will bring a strong background in oncology research project ...