Clinical Scientist Program Lead - Cellular Therapy

Working with UsChallenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible.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. Read more: careers.bms.com/working-with-us.Description: The Clinical Scientist Program Lead reports through the Clinical Science function which provides scientific expertise necessary to design and deliver clinical studies and programs.Position Summary/Objectives: Partners with VP/Clinical Scientist Head to plan, lead, and advance programs and talent.Serves as a member of the Clinical Science Leadership Team and Development TeamSupports resource forecasting, talent development, succession planning and retention strategiesDefines and standardizes best practices and development opportunities for the scientist teamBuilds a collaborative, supportive learning environmentEnsures and contributes to a consistent and high level of training for Clinical Scientists across the department with respect to relevant scientific data and knowledge, including SOPs and Working PracticesMay serve as a delegate of Clinical Scientist Head as neededPartners with the Clinical Development Lead accountable for the assigned program; supports activities required to develop clinical development and lifecycle management plansResponsibilities: Leads a team or complex scope of work to ensure high quality delivery of innovative protocols and data packages for CSRs and Regulatory FilingsOversees all clinical studies within assigned program(s) to ensure consistency across program(s)Ensures high quality and timely delivery of protocols and data; implements quality assurance plansMaintains an advanced understanding of the status of all trial activities within assigned ProgramProvides scientific and clinical leadership to support the team; provide program/study/therapeutic area/skills training to team membersAttends Development Team meetings as neededLeads resourcing and budget planning activities for teamHolds accountability for the performance and professional development of Clinical Scientist teamLeads proactive risk identification and mitigation plans; provides progress reports and risk assessment updates to Sr. ManagementReviews and approves clinical contributions to all trial documents / abstracts / publicationsReviews, audits, and presents data and information to internal leaders and external investigatorsServes as a key cross functional collaborator; represents the Clinical Scientist function in various process improvement initiatives and/or cross functional activitiesCollaborates to support incoming asset and/or business development activities (i.e., due diligence)Degree Requirements: Degree in Life Sciences (MD, PhD, Pharm D, MS, RN or other scientific field preferred)Experience Requirements: 15+ years of experience in clinical science, clinical research, or equivalentExperience working on assets for malignant and non-malignant hematological disorders including myelodysplastic syndrome, myelofibrosis, thalassemia, etcExtensive experience and demonstrated proficiency in managing direct/indirect employees and leading teamsKey Competency RequirementsExpertise in GCP/ICH, drug development process, study design, statistics, clinical operationsRecognized internally and externally as a Functional/Technical expertAdvanced ability to analyze, interpret, and present dataAdvanced knowledge and skills to support program specific data review, trend identification, data interpretationExpertise in of indication, therapeutic area, compound(s), competitive landscape and health authority requirementsAbility to act independently to identify/resolve and lead team towards resolving program level issuesStrong critical thinking, problem solving, decision making skillsAdvanced oral and written communication skills, including medical writing, presentations to large groups, facilitation of interactive discussions and 1:1 discussion with internal and external thought leadersDemonstrated strong leadership presenceExpert financial acumenCommitment to QualityAdaptable / FlexibleExhibits confidence and professional diplomacy, while effectively relating to people at all levels internally and externallyPromotes a culture of scientific excellence, multidisciplinary problem solving, teamwork, consistency, flexibility, execution, quality and effective communicationAnticipates needs, assesses and manages business and organizational risksTravel: Domestic and International travel may be required.If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.Uniquely Interesting Work, Life-changing CareersWith a single vision as inspiring as “Transforming patients’ lives through science ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.On-site ProtocolPhysical presence at the BMS worksite or physical presence in the field is a necessary job function of this role, which the Company deems critical to collaboration, innovation, productivity, employee well-being and engagement, and it enhances the Company culture.BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.