Senior Research Investigator

Profile

Bristol-Myers Squibb is a global Biopharma company committed to a single mission: to discover, develop, and deliver innovative medicines focused on helping millions of patients around the world in disease areas such as oncology, cardiovascular, immunoscience and fibrosis.

Join us and make a difference. We hire the best people and provide them with a work environment that places a premium on diversity, integrity, collaboration and personal development. Through a culture of inclusion, we create a better, more productive work environment. We believe that the diverse experiences and perspectives of all our employees help to drive innovation and transformative business results.


Contribute to the development of compounds developed across multiple therapeutic areas including but not limited to immunology, cardiovascular, virology, fibrosis, and neuroscience

Contribute towards the creation of CP&P development plans and execution of CP&P related deliverables that are aligned with the strategic objectives of the development team

Lead / Contribute to the design of clinical studies to characterize the pharmacokinetic, pharmacodynamic, and drug metabolism properties, as well as analyze, interpret and report data from such studies

Plan, execute, and report on model-based pharmacokinetic and exposure-response analyses of data from clinical studies

Represent the CP&P function on cross-functional drug development teams, contribute to regulatory submissions, and participate in interactions with health authorities

Participate in departmental initiatives and represent CP&P on cross-functional initiatives / workstreams / taskforces
The colleague will have / be able to



knowledge of current practices and issues in clinical pharmacology and pharmacometrics

strong written and oral communication skills necessary to report on and deliver scientific presentations

demonstrate the ability to work in a dynamic team oriented environment

Serve as the CP&P lead for one or more assets in the BMS drug development program, with supervision


Position Responsibilities

The colleague will have / be able to


knowledge of current practices and issues in clinical pharmacology and pharmacometrics

strong written and oral communication skills necessary to report on and deliver scientific presentations

demonstrate the ability to work in a dynamic team oriented environment

Serve as the CP&P lead for one or more assets in the BMS drug development program, with supervision


Degree Requirements

A PharmD or PhD in pharmaceutical sciences, pharmacology, biomedical engineering, or a related field.

Experience Requirements

2 years of experience in clinical pharmacology and pharmacometrics, including experience in characterizing the pharmacokinetic and pharmacodynamic (biomarker/safety/efficacy) properties of small molecule and biologics drugs

Key Competency Requirements

Experience with the following software is highly desired: R, NONMEM, MONOLIX, and WinNonlin.

Travel Required

Local and international travel for conferences and regulatory meetings may be required depending on project needs up to 5-10% of the time

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.

Bristol-Myers Squibb is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

Company info

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