Sr. Clinical Trial Physician

Bristol Myers Squibb

Madison, NJ, US
Base: $243,930 - $295,589; bonus/equity: + incenti...
Hybrid (50% onsite)
Md degree required
5+ years industry clinical trials experience
Medical accountability for multiple trials
Bristol Myers Squibb is seeking a Senior Clinical Trial Physician to oversee multiple clinical trials, ensuring medical accountability and strategic input throughout the drug development process. The ideal candidate will have a strong background in clinical trials, an MD degree, and extensive experience in the pharmaceutical industry

Job Summary

  • The Senior Clinical Trial Physician serves as the primary source of medical accountability and oversight for multiple Phase 1 through Phase 3 clinical trials.
  • This role involves designing clinical plans, leading benefit/risk analyses, and collaborating with cross-functional teams to ensure regulatory and disease strategy targets are met.
  • Bristol Myers Squibb offers a comprehensive benefits package including health coverage, financial protection, flexible time off, and opportunities for global participation in clinical trials.

Matching Summary

Match Score: 85

Bristol Myers Squibb is seeking a Senior Clinical Trial Physician to oversee multiple clinical trials, ensuring medical accountability and strategic input throughout the drug development process. The ideal candidate will have a strong background in clinical trials, an MD degree, and extensive experience in the pharmaceutical industry.

Salary

Base: $243,930 - $295,589; Bonus/Equity: Additional incentive cash and stock opportunities available; Benefits: Medical, dental, vision, 401(k), paid time off, and wellness programs

Skills & Requirements

Must-have

  • MD degree required
  • 5+ years industry clinical trials experience
  • Medical accountability for multiple trials
  • Protocol development and strategic oversight
  • Safety assessment of serious adverse events

Nice-to-have

  • Subspecialty training in therapeutic area
  • Strong leadership in matrix team environment
  • Expertise in statistical design and analysis
  • Relationship building with principal investigators
  • Knowledge of competitive landscape and biomarkers

Key Requirements

  • MD or US equivalent degree
  • Minimum 5 years of industry or clinical trials experience
  • Expertise in drug development process and GCP compliance
  • Ability to lead presentations in scientific settings

Work Rights

Not specified

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