VP and Clinical Trial Strategy & Ops - NRDG & I

Princeton, NJ, United States
Sep 25, 2020
Required Education
Bachelors Degree
Position Type
Full time
At Bristol Myers Squibb, we are inspired by a single vision - transforming patients' lives through science.In oncology, hematology, immunology and cardiovascular disease - and one of the most diverse and promising pipelines in the industry - each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference.


Head of Global Clinical Trial Strategy & Operations - Non-Registrational Development will provide strategic and operational leadership of the late phase and non-registrational studies portfolio within GDO.
Responsibilities:• Oversee the implementation of the strategy for five areas - solid tumors, hematology, immunology/fibrosis, cardiovascular and CAR-T during their duration within late stage development and non-registrational trial conduct.• Drive the performance, operational quality, innovative development strategies/trial designs, and the timely contributions of GDO's support to commercial and medical• Partner with therapeutic area heads, commercial and medical heads to provide oversight and leadership that ensures late stage teams design and execute programs that enable data generation of integrity and quality to support market claims, successful market access and generate valuable data for medical communication• Lead a USA team of clinical trial professionals, who are experts in the execution of clinical trial operations, and contribute significantly to BMS portfolio of clinical trials• Ensure GDO representation as needed in governance or strategic teams or committees (preparatory materials, direct participation, or representative)• Provide ongoing feedback, coaching, and career development, including engagement and retention support to staff in order to maximize their potential


• Advanced degree preferred; 15+ years of relevant industry experience• Recognized skill in managing drug development across all phases of development and TAs• Experience in design and execution of multiple study types to generate data (investigator initiated studies, cooperative group studies, non-interventional research, expanded access programs, etc.)• Experience in leading global clinical trial programs across major worldwide markets, including experience with CROs

Around the world, we are passionate about making an impact on the lives of patients with serious diseases. Empowered to apply our individual talents and diverse perspectives in an inclusive culture, our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.

Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives.