Bristol-Myers Squibb Company

Senior Research Investigator

Location
Princeton, NJ, US
Posted
Oct 29, 2018
Ref
R1508503
Required Education
Doctorate/PHD/MD
Position Type
Full time
Bristol-Myers Squibb is a global biopharmaceutical company whose mission is to discover, develop and deliver innovative medicines that help patients prevail over serious diseases.

One shared journey is moving us forward at Bristol-Myers Squibb. Around the world, we are passionate about making an impact on the lives of patients with serious disease. Empowered to apply our individual talents and ideas so that we can learn and grow together. Driven to make a difference, from innovative research to hands-on community support. 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 the resources to pursue their goals, both at work and in their personal lives.

Position Description:

In this role, you will contribute to the development of anti-cancer compounds by leading the design of clinical studies to characterize the pharmacokinetic, pharmacodynamic, and drug metabolism properties of these compounds, as well as the analysis, interpretation and reporting of data from such studies. You will also plan, execute, and report on model-based pharmacokinetic and exposure-response analyses of data from clinical studies. In addition, you will represent the clinical pharmacology and pharmacometric functions on cross-functional drug development teams, contribute to regulatory submissions, and participate in interactions with health authorities.

Position Requirements:
  • A PhD or PharmD in pharmaceutical sciences or a related field, with a minimum of 3 years' industry experience in the design, conduct, and reporting of clinical pharmacology studies and performing and reporting pharmacometric analyses.
  • The successful candidate will have in-depth knowledge of ADME and pharmacokinetics.
  • Must be knowledgeable with current practices and guidelines in clinical pharmacology and hands-on experiences with pharmacometric analyses
  • Strong written and oral communication skills necessary to report on and deliver scientific presentations.
  • Demonstrated the ability to work in a dynamic team oriented environment.
  • Experience with the following software is highly desired: NONMEM, R, and Simcyp.