PpbDescription /b /p /p pThe Global Clinical Physician sits within Clinical Development, which is a global organization dedicated to the effective design and execution of drug development. Clinical Development drives clinical development strategy, design, execution, and interpretation of clinical trials. /ppbPosition Summary / Objective /b /pliServes as a primary source of medical accountability and oversight for clinical trials /liliMatrix management responsibilities across the internal and external network /liliManages Phase 1 – Phase 3 studies, with demonstrated decision making capabilities /liliProvides medical and scientific expertise to cross-functional BMS colleagues /lipbPosition Responsibilities /b /ppMedical Monitoring /pliContributes to and is a key member of a high performing Study Delivery Team (SDT) and may be a member of the Clinical Development Team (CDT) /liliConducts medical data review of trial data, including eligibility review /liliHolds responsibility for site interactions in partnership with the Global Clinical Scientist (GCS) for medical questions and education (including safety management guidelines) /liliHolds responsibility for assessment of key safety-related serious adverse events in partnership with Worldwide Patient Safety and oversees safety narratives /liliCollaborates with GCS and inputs into protocols, providing medical strategic oversight in protocol development (input on inclusion/exclusion and other safety-related clinical considerations) /liliFulfills GCP and compliance obligations for clinical conduct and maintains all required training /lipClinical Development Expertise Strategy /pliIn collaboration with the Global Clinical Development Lead, designs and develops clinical plans and protocols with a strong strategic focus based on knowledge of asset/drug, disease area and relevant science in order to meet regulatory and disease strategy targets /liliProvides oversight and medical accountability for a group of studies /liliLeads the analysis of benefit/risk for clinical development protocols in a matrix team environment working with GCS /liliPartners with GCS to support executional delivery of studies (e.g., site activation, enrollment status, as well as adjudication for protocol violations, significant, non-significant deviations etc.) /liliIdentifies and builds relationships with principal investigators. Identifies and cultivates thought leaders in order to gain their inputs on emerging science in drug and biomarker research, disease knowledge, and design of clinical development studies and programs /liliMaintains a strong medical/scientific reputation within the disease area. Has in-depth knowledge of etiology, natural history, diagnosis, and treatment of the disorder. Keeps up-to-date in the disease area by attending scientific conferences and ongoing review of the literature /liliKeeps abreast of development and regulatory issues related to other competitive or relevant compounds in development and how our portfolio fits into the competitive landscape /liliProvides ongoing medical education in partnership with GCS to allow for protocol-specific training, supporting the study team, investigators, and others /lipHealth Authority Interactions Publications /pliContributes to key Health Authority interactions and advisory board meetings as Global Clinical Physician /liliAuthors/drafts clinical content for CSRs, regulatory reports, briefing books and submission documents to support closure, clinical narratives, reporting and filling of the study in partnership with Global Clinical Scientists /lipbDegree Requirements /b /ppMD required (or x-US equivalent) /ppbRequirements /b /pli3 or more years of Industry experience and/or clinical trials experience is required /liliAbility to communicate and present information clearly in scientific and clinical settings /liliSubspecialty training in applicable therapeutic area desired /liliExpertise in the scientific method to test hypotheses, including statistical design, analysis, and interpretation /liliKnowledge of drug development process /liliKnowledge of the components needed to execute an effective clinical plan and protocols /liliStrong leadership skills with proven ability to lead and work effectively in a team environment /liliDomestic and International travel may be required. /lipbUniquely Interesting Work, Life-changing Careers /bbr/With 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 a supportive culture, promoting global participation 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. /ppbOn-site Protocol /b /ppBMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role: /ppSite-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function. /ppbSupporting People with Disabilities /b /ppBMS 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 to access our complete Equal Employment Opportunity statement. /ppbCandidate Rights /b /ppBMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area. /ppbData Protection /b /ppAny data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations. /pR : Director, Global Clinical Physician