Director, Global Clinical Physician

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You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. 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.

Clinical Development drives clinical development strategy, design, execution, and interpretation of clinical trials.Position Summary / ObjectiveServes as a primary source of medical accountability and oversight for clinical trialsMatrix management responsibilities across the internal and external networkManages Phase 1 – Phase 3 studies, with demonstrated decision making capabilitiesProvides medical and scientific expertise to cross‑functional BMS colleaguesPosition ResponsibilitiesMedical MonitoringContributes 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)Conducts medical data review of trial data, including eligibility reviewHolds responsibility for site interactions in partnership with the Global Clinical Scientist (GCS) for medical questions and education (including safety management guidelines)Holds responsibility for assessment of key safety‑related serious adverse events in partnership with Worldwide Patient Safety and oversees safety narrativesCollaborates with GCS and inputs into protocols, providing medical strategic oversight in protocol development (input on inclusion/exclusion and other safety‑related clinical considerations)Fulfills GCP and compliance obligations for clinical conduct and maintains all required trainingClinical Development Expertise & StrategyIn 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 targetsProvides oversight and medical accountability for a group of studiesLeads the analysis of benefit/risk for clinical development protocols in a matrix team environment working with GCSPartners 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.)Identifies and builds relationships with principal investigators.

Keeps up‑to‑date in the disease area by attending scientific conferences and ongoing review of the literatureKeeps abreast of development and regulatory issues related to other competitive or relevant compounds in development and how our portfolio fits into the competitive landscapeProvides ongoing medical education in partnership with GCS to allow for protocol‑specific training, supporting the study team, investigators, and othersHealth Authority Interactions & PublicationsContributes to key Health Authority interactions and advisory board meetings as Global Clinical PhysicianAuthors/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 ScientistsDegree RequirementsMD required (or x-US equivalent)Requirements3 or more years of Industry experience and/or clinical trials experience is requiredAbility to communicate and present information clearly in scientific and clinical settingsSubspecialty training in applicable therapeutic area desiredExpertise in the scientific method to test hypotheses, including statistical design, analysis, and interpretationKnowledge of drug development processKnowledge of the components needed to execute an effective clinical plan and protocolsStrong leadership skills with proven ability to lead and work effectively in a team environmentDomestic and International travel may be required.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.

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. Take your career farther than you thought possible.Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment.

Read more: Website Area DescriptionThe Global Clinical Physician sits within Clinical Development, which is a global organization dedicated to the effective design and execution of drug development.

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 programsMaintains a strong medical/scientific reputation within the disease area.

Has in‑depth knowledge of etiology, natural history, diagnosis, and treatment of the disorder.

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.On‑site ProtocolBMS 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: Site-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.Supporting People With DisabilitiesBMS 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 Website to access our complete Equal Employment Opportunity statement.Candidate RightsBMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: Website ProtectionWe will never request payments, financial information, or social security numbers during our application or recruitment process.

Learn more about protecting yourself at Website data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at Please provide the Job Title and Requisition number so we can review.

Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.R : Director, Global Clinical Physician