Position Title: Senior Director, Clinical Development Lead - NeuroscienceCompany: Bristol-Myers SquibbLocation: Madison-NJ Position Summary / Objective CDLs are matrix leaders and managers who lead, develop, motivate, and achieve results through teams; demonstrate a commitment to the development of a resilient attitude, embrace change and have an unwavering commitment to our People Strategy. Serves as the clinical point of accountability for the Development Team and is responsible for the overall clinical development plan for asset(s) in one or more indication(s)/tumor type(s). Ensures studies are aligned with target label indications and are designed to meet regulatory, quality, medical, and access goals. Serves as a matrix leader to lead, develop, motivate and achieve results through teams, and is the direct manager to Clinical Trial Physicians (CTPs). Position Responsibilities Accountable for the clinical contribution to the development of each indication strategy, including registrational and non-registrational studies, with the support of the CTPs and Clinical Scientists (CS) within the asset and/or indication. Responsible for managing clinical trial physician(s); attracting, developing and retaining top talent; ensuring appropriate training and mentoring of clinical trial physicians. May serve as CTP as necessary. Accountable in partnership with the Clinical Scientist for the design, execution, and analyses of each study led by the CTPs and CSs. Should work to proactively partner with these roles. Accountable for clinical content for CSRs, regulatory reports, briefing books and submission documents. Champions a quality-focused mindset and ensures adherence to GCP and compliance obligations for clinical conduct. Represents Clinical Development in both internal and external forums as the consulted authority for the disease area, including within Business Development function. Partners with Worldwide Patient Safety physicians in the ongoing review of safety data. Serves as the (co-)leader of the cross-functional Clinical Development Team. Provides clinical leadership and disease area expertise into integrated disease area strategies. Partners closely with KOLs in specific indications. Serves as Primary Clinical Representative in Regulatory interactions. Evaluates strategic options against a given Target Product Profile (TPP). Collaborates with Global Development Operations/Global Compliance Group to develop asset level risk management plan, resolves issues with Quality/CS, and raises to DT as needed. Sets executional priorities and partners with CTP and CS to support executional delivery of studies. Accountable for top line data with support of CTP, CS, and Statisticians. Degree Requirements MD preferably with appropriate sub-specialty training as appropriate. PhD, Pharm D or other health related scientific field with a deep understanding of the clinical principles of the area of interest or equivalent therapy area knowledge. At least 9 years of relevant experience. Experience Requirements CDL has demonstrated leadership in the design and execution of multiple clinical trials (e.g. significant experience as a senior clinical leader), and exhibits all of the following attributes: Able to synthesize internal and external data to produce a clinical strategy. Able to ensure that the clinical program will result in a viable registrational strategy. Able to assess personnel needs, translate into a hiring strategy, and lead the hiring efforts. Able to work with other stakeholders to ensure a robust enterprise level strategy for asset(s) and indication(s) including early, late and post-marketing development, as well as awareness of the enterprise disease area portfolio. CDL has demonstrated, sustained excellent performance as Clinical Trial Physician, Clinical Scientist, or equivalent. Verifiable track record of successful people management and development, or leadership in a matrix team (e.g., mentoring junior colleagues). Key Competency Requirements CDL has demonstrated excellent skills in clinical development strategy including the clinical components of regulatory submission(s). External focus to understand the trends in the disease area treatment paradigms and ability to build relationships with external partners, thought leaders and collaborators outside of BMS. Partner and interact with colleagues from Early Development who design and implement first in human through proof of concept trials and will to assure a seamless transition into late stage development (Phase II-III trials). Ability to lead and develop a group of CTPs to ensure scientific and technical excellence of clinical development programs and deliverables. Travel Required Domestic and International travel may be required. Compensation Overview Civil Cambridge Crossing: $350,780 - $425,060Madison – Giralda – NJ – US: $313,200 – $379,524Princeton – NJ – US: $313,200 – $379,524 The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee's work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience. Benefit Offerings Health Coverage: Medical, pharmacy, dental, and vision care. Wellbeing Support: Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs. Financial and Protection: 401(k) plan, disability, life and accident insurance, supplemental health insurance, travel protection, liability protection, identity theft support, legal support, and survivor support. Equal Opportunity Statement Bristol Myers Squibb is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran status, pregnancy, citizenship, marital status, gender expression, genetic information, political affiliation, or any other characteristic protected by law. #J-18808-Ljbffr