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Sr. Clinical Trial Physician, Neuropsychiatry

Job in Cambridge, Middlesex County, Massachusetts, 02140, USA
Listing for: Bristol Myers Squibb
Full Time position
Listed on 2026-03-01
Job specializations:
  • Doctor/Physician
    Medical Doctor, Healthcare Consultant
Salary/Wage Range or Industry Benchmark: 125000 - 150000 USD Yearly USD 125000.00 150000.00 YEAR
Job Description & How to Apply Below

Position Summary / Objective

Position Title: Sr. Clinical Trial Physician, Neuropsychiatry. The Clinical Trial Physician sits within Clinical Development, a global organization focused on the design and execution of drug development. Clinical Development drives clinical development strategy, design, execution, and interpretation of clinical trials.

Position Responsibilities
  • Medical Monitoring:
    Contribute to and be a key member of a high performing Study Delivery Team (SDT) and may be a member of the Clinical Development Team (CDT); lead medical data review of trial data, including eligibility review; manage site interactions in partnership with the Clinical Scientist for medical questions and education (including safety management guidelines); assess key safety-related serious adverse events in partnership with Worldwide Patient Safety and oversee safety narratives;

    provide medical strategic oversight in protocol development (input on inclusion/exclusion and other safety-related clinical considerations); fulfill GCP and compliance obligations for clinical conduct and maintain all required training.
  • Clinical Development Expertise & Strategy:
    In collaboration with the Clinical Development Lead, design and develop clinical plans and protocols with a strong strategic focus based on asset/drug knowledge, disease area, and relevant science to meet regulatory and disease strategy targets; provide oversight and medical accountability for a group of studies; lead benefit/risk analysis for clinical development protocols in a matrix team environment with Clinical Scientists;

    partner with CS to support executional delivery of studies (site activation, enrollment status, adjudication for protocol violations and deviations); identify and engage principal investigators and thought leaders to obtain inputs on emerging science, disease knowledge, and study design; maintain a strong medical/scientific reputation within the disease area and stay current with etiology, natural history, diagnosis, and treatment; monitor regulatory issues and competitive landscape;

    provide ongoing medical education with CS for protocol-specific training to support the study team, investigators, and others.
  • Health Authority Interactions & Publications:
    Serve as medical point of expertise in Health Authority interactions and advisory board meetings; author/draft clinical content for CSRs, regulatory reports, briefing books, and submission documents in partnership with CSs.
Education & Experience
  • Degree Requirements
    : MD required (or x-US equivalent).
  • Experience Requirements
    : 5 or more years of clinical trial experience, either in industry or academic setting.
Key Competency Requirements
  • Ability to communicate information clearly and lead presentations in scientific and clinical settings
  • Subspecialty training in applicable therapeutic area desired
  • Expertise in the scientific method to test hypotheses, including statistical design, analysis, and interpretation
  • Expertise in the drug development process
  • Expertise in the components needed to execute an effective clinical plan and protocols
  • Strong leadership skills with demonstrated ability to lead and work effectively in a team environment
Travel

Domestic and international travel may be required.

Compensation & Benefits

The starting compensation range(s) are listed by location for a full-time employee. Additional incentive cash and stock opportunities may be available. Final compensation is based on demonstrated experience. Eligibility for specific benefits varies by job and location. Benefits may include health coverage, wellbeing programs, financial protection plans, and work-life programs. For more details, visit the careers site.

  • Health Coverage:
    Medical, pharmacy, dental, and vision care
  • Wellbeing & Financial Well-being:
    Programs such as wellbeing accounts, EAP, 401(k) and related protections
  • Paid Time Off:
    Flexible time off (US exempt), holiday schedule, and location-based variations

On-site/Work Model
: BMS occupancy framework indicates site-essential, site-by-design, field-based, and remote-by-design roles with variation in onsite requirements and possible hybrid arrangements.

Additional Information

If you encounter a role that intrigues you but doesn’t perfectly align with your resume, we encourage you to apply. You could be one step away from work that will transform your life and career.

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