Research Investigator II - Toxicology

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.

Developmental and Reproductive Toxicologist

Play a strategic role on technical/investigative/mechanistic investigative teams; implement new approaches, processes, and technologies as part of toxicologic evaluations.

Assume responsibilities as a Study Director/Monitor, for regulatory, exploratory, and investigative, reproductive, or developmental toxicology studies, including study design and protocol development, as well as data evaluation and reporting in a GLP environment.

Serve as toxicology project manager on multidisciplinary drug development teams, including generation of integrated summary documents, health authority interactions, and ensure timely and appropriate nonclinical toxicology data delivery and communication.

Integrate data within and across studies to provide risk assessment and context to toxicology study outcomes. Keep abreast of relevant scientific literature.

Develop deep understanding of regulatory guideline in vivo and in vitro evaluations of toxicity testing for pharmaceuticals and biologics.

Serve as a key contributor to discovery/development projects as a subject matter expert.

Embrace/demonstrate BMS Core Behaviors of Passion, Innovation, Speed, and Accountability.

Ensure compliance with all company/departmental policies, particularly those relating to animal welfare and employee safety and health

Qualifications

Ph.D. in relevant discipline (Toxicology, Developmental Biology, Pharmacology, Physiology, or similar field). 0-3 years' working experience as an investigator or GLP study director; postdoctoral experience required. Evidence of professional presence at the regional/national level, as evidenced by publication record, professional meeting presentations, and/or professional honors. Skills to include in vivo and/or in vitro capabilities to examine mechanisms of drug-induced toxicity. Ability to work in a fast-paced team-based environment, across multiple disciplines and departments, managing multiple studies/projects simultaneously. Strong written and oral presentation skills.