Sr Clinical Trial Physician II Cardiovascular - ...

, ATTENTION MILITARY AFFILIATED JOB SEEKERS, - Our organization works with partner companies to source qualified talent for their open roles. The following position is available to, Veterans, Transitioning Military, National Guard and Reserve Members, Military Spouses, Wounded Warriors, and their Caregivers. If you have the required skill set, education requirements, and experience, please click the submit button and follow the next steps. Unless specifically stated otherwise, this role is 'On-Site' at the location detailed in the job post.Position SummaryThe Senior Clinical Trial Physician II is the primary source of medical accountability and oversight for one or more cardiovascular clinical trials within the Drug Development organization. The incumbent will be accountable, alongside the Clinical Development Program Lead, for the development of differentiated and strategic clinical development plans from phase I expansion through to registrational execution. They will be foundational in working with teams in Research, Early and Late Development, providing insights into biology, translational elements, as well as overall benefit risk assessments. This role includes support of cross-portfolio activities in line with Clinical Excellence, including Protocol Review Committee, support of Business Development activities and Quality and compliance leadership.The Senior Clinical Trial Physician II 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. The Sr CTP II will report directly to the Clinical Development Program Lead or Head of Clinical Development.Key Responsibilities⢠Serves as a primary source of medical accountability and oversight for multiple clinical trials or a single trial with significant complexity within Cardiovascular Clinical Development group⢠Supervises the development, monitoring, analysis, and interpretation of clinical trials and will supervise and have accountability for the clinical components of regulatory filings.⢠Will contribute to overall Therapeutic Area disease strategy while ensuring an overall portfolio view⢠Provides strategic insights into clinical development plans⢠Provides medical and scientific expertise to cross-functional BMS colleagues⢠Matrix management responsibilities across the internal and external network⢠Manages Phase 1 to Phase 3 clinical studies, with demonstrated decision-making capabilities⢠The role will be foundational in working with teams in Research, Early and Late Development teams to support gated investment decisions and transitions, providing insights into biology, translational elements as well as overall benefit risk assessmentsClinical Development Expertise ,Strategy:, ⢠A Senior Clinical Trial Physician II is a tenured drug developer who can independently design and construct clinical development 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.⢠Done in conjunction with Clinical Development Program Lead or as a delegate when CDPL is not assigned⢠Extensive experience in Research and Development (late and/or early development) and across various Phases of study design⢠Respected for Disease Expertise (internal to BMS and within the medical community)⢠Disease Lead- able to serve as internal consultant for respective disease(s) based on scientific knowledge and therapeutic expertise⢠Provides oversight and medical accountability for a group of high-priority studies⢠Leads the analysis of benefit/risk for clinical development protocols in a matrix team environment working with Clinical Scientists (CS)⢠Partners with CS to support executional delivery of studie⢠Existing strong 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⢠Keeps abreast of development and regulatory issues related to other competitive or relevant compounds in development and how our portfolio fits into the competitive landscape⢠Senior CTP II should be able to anticipate impact of external data which may shift internal clinical strategy and proactively assess needs for internal program (ie amendments, need for ad hoc analyses ,implications to execution of internal programs)⢠Provides ongoing medical education in partnership with collaborating Clinical Scientists to allow for protocol-specific training, supporting the study team, investigators, and internal stakeholdersMedical Monitoring:⢠Leader of high performing Study Delivery Team (SDT) and key member of the Clinical Development Team (CDT)⢠Study-Leader with ability to own/drive study level strategic decisions⢠Leads medical data review of trial data, including eligibility review⢠Holds responsibility for site interactions in partnership with the Clinical Scientist (CS) 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 narratives⢠Leads collaboration with CS 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 training⢠Onboarding Lead ⓠprovides guidance and training to new CTP (not limited to data management; systems training), therapeutic training, innovative study design and sets example of high proficiency for the organizationHealth Authority Interactions ,Publications:⢠Serves as medical point of expertise in key Health Authority interactions and advisory board meetings as Clinical Trial Physician⢠Authors 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 CSs⢠Experience with regulatory submission ,development of clinical sections in regulatory documents for submission across several markets⢠Ability to lead strategic framework for clinical sections of regulatory documents⢠Exceptional clinical response strategist for queries (written ,oral) Stakeholder Engagement and Communication⢠Be recognized internally and externally as an expert in the field.⢠Partner and interact with colleagues from Research and Early Development who design and implement first in human through proof-of-concept trials and will assure a seamless transition into late-stage development (Phase II-III trials.)⢠Ability to influence leadership and upper management of key functions, applying foresight, scientific and development knowledge to ensure support of late clinical development needs and adequacy of clinical studies leading to registration, , , , , ,

Created: 2026-02-13