Senior Research Investigator Clinical Pharmacology

Profile

At Bristol Myers Squibb, we are inspired by a single vision - transforming patients' lives through science.In oncology, hematology, immunology and cardiovascular disease - and one of the most diverse and promising pipelines in the industry - each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference.

Position Summary / Objective


Responsible for design and execution of Clinical Pharmacology activities and works on assigned projects.
Leads, plans, and executes trial level activities and development of compounds across therapeutic areas while managing data analysis.
Applies Pharmacokinetics/Pharmacodynamics principles and model-based analyses to support drug development.
Collaborates within Clinical Pharmacology and cross-functionally to assist with functional development strategies.


Position Responsibilities


Contribute to the development of compounds across various therapeutic areas with some supervision
Lead design of Clinical Pharmacology studies and manage data analysis, interpretation, and reporting
With some supervision, contribute to clinical development strategies of pipeline product
Proficient in PK, PK/PD, and Model Informed Drug Development (MIDD) principles and analyses
Acquires and interprets PK/PD with some supervision
Participate in interactions with health authorities
Contribute to and/or lead modeling and simulation plan
Collaborate on cross-functional drug development teams, regulatory submissions, and departmental initiatives


Degree Requirements

MS, PhD or PharmD in relevant field

Experience Requirements

Approximately 2 years' experience with demonstrated progression in Clinical Pharmacology and Pharmacometrics knowledge, including general knowledge of general drug development process

Key Competency Requirements


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
Demonstrated 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
Programming experience is highly desired (e.g., NONMEM, R, and WinNonlin. SAS, Splus, etc.)
Quantitative data analysis, POP PK/PD, and data visualization skills are highly desired


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

Around the world, we are passionate about making an impact on the lives of patients with serious diseases. Empowered to apply our individual talents and diverse perspectives in an inclusive culture, our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.

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 with the resources to pursue their goals, both at work and in their personal lives.

Company: Bristol-Myers Squibb

Req Number: R1526976_EN

Updated: 2020-07-01 00:00:00.000 UTC

Location: Jersey City,New Jersey

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, age, disability, protected veteran status, pregnancy, citizenship, marital status, gender expression, genetic information, political affiliation, or any other characteristic protected by law.

Company info

Sign Up Now - MiamiCrossing.com