Research Investigator, Clinical Pharmacology
Bristol Myers Squibb
August 17, 2026
Remote friendly (Princeton, NJ)
United States
Clinical Research and Development
Position Summary:
The Research Investigator supports execution of Clinical Pharmacology activities, collaborating with departmental mentors to contribute to assigned projects. Applies pharmacokinetics/pharmacodynamics expertise and model-based analyses to inform drug development decisions.
Key Responsibilities:
- Contribute to compound development and design of clinical studies across therapeutic areas (with supervision)
- Contribute to clinical development strategies of pipeline products (with supervision)
- Develop proficiency in PK, PK/PD, and Model Informed Drug Development (MIDD) principles and analyses
- Contribute to acquisition and interpretation of PK/PD data
- Participate in interactions with health authorities
- Contribute to modeling and simulation plans
- Collaborate with cross-functional teams on drug development, regulatory submissions, and departmental initiatives
Qualifications & Experience:
- MS, PhD, or PharmD in a relevant field
- Knowledge of current practices and issues in Clinical Pharmacology and Pharmacometrics
- Strong written and oral communication skills; ability to deliver scientific presentations
- Demonstrated ability to work in a dynamic, team-oriented environment
- Programming experience highly desired (NONMEM, R, WinNonlin; SAS, Splus, etc.)
- Basic quantitative data analysis, POP PK/PD, and data visualization highly desired
Compensation (Princeton, NJ, US): $122,460–$148,392.
Benefits (highlights): Health coverage (medical/pharmacy/dental/vision); wellbeing support; 401(k) and insurance/disability benefits.
On-site Protocol (essential job function): Site-essential = 100% onsite shifts; site-by-design = hybrid with at least 50% onsite.
The Research Investigator supports execution of Clinical Pharmacology activities, collaborating with departmental mentors to contribute to assigned projects. Applies pharmacokinetics/pharmacodynamics expertise and model-based analyses to inform drug development decisions.
Key Responsibilities:
- Contribute to compound development and design of clinical studies across therapeutic areas (with supervision)
- Contribute to clinical development strategies of pipeline products (with supervision)
- Develop proficiency in PK, PK/PD, and Model Informed Drug Development (MIDD) principles and analyses
- Contribute to acquisition and interpretation of PK/PD data
- Participate in interactions with health authorities
- Contribute to modeling and simulation plans
- Collaborate with cross-functional teams on drug development, regulatory submissions, and departmental initiatives
Qualifications & Experience:
- MS, PhD, or PharmD in a relevant field
- Knowledge of current practices and issues in Clinical Pharmacology and Pharmacometrics
- Strong written and oral communication skills; ability to deliver scientific presentations
- Demonstrated ability to work in a dynamic, team-oriented environment
- Programming experience highly desired (NONMEM, R, WinNonlin; SAS, Splus, etc.)
- Basic quantitative data analysis, POP PK/PD, and data visualization highly desired
Compensation (Princeton, NJ, US): $122,460–$148,392.
Benefits (highlights): Health coverage (medical/pharmacy/dental/vision); wellbeing support; 401(k) and insurance/disability benefits.
On-site Protocol (essential job function): Site-essential = 100% onsite shifts; site-by-design = hybrid with at least 50% onsite.