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Senior Clinical Trial Physician II, Cardiovascular

Job in Cambridge, Middlesex County, Massachusetts, 02140, USA
Listing for: Bristol Myers Squibb
Full Time position
Listed on 2026-02-18
Job specializations:
  • IT/Tech
    Medical Imaging
Salary/Wage Range or Industry Benchmark: 60000 - 80000 USD Yearly USD 60000.00 80000.00 YEAR
Job Description & How to Apply Below

Working with Us

Challenging. 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. 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:  .

Position Summary

The 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 assessments
Clinical 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…
Position Requirements
10+ Years work experience
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