Senior Associate Scientist, In Vivo Pharmacology (Non-PhD)

Location
Redwood City, CA
Posted
May 15, 2022
Ref
R1557542
Required Education
Bachelors Degree
Position Type
Full time

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.

The Tumor Microenvironment Thematic Research Center (TME TRC) is focused on developing therapeutic targets at the intersection of stromal, tumor and immune biology that enhance responsiveness to checkpoint blockade and other targeted therapies and transform response and durability rates for cancer patients. Our team comprises of scientists across multiple disciplines who are responsible for the biology and translational science necessary to support drug development from target identification through to first in human studies.

The In Vivo Pharmacology (IVP) Group within the TME TRC is dedicated to developing the IVP strategy and designing and executing on the IVP studies required to progress all the TME TRC preclinical drug development programs (both small and large molecule) from validation through to candidate selection and beyond.

In this role you will provide technical expertise in in vivo study planning and execution, participate in data interpretation and presentation. You will effectively collaborate with colleagues in IVP and with colleagues in cross-functional groups at TME TRC (discovery and translational research) and other supportive line functions (biotherapeutics, predictive science, and small molecule drug development)

Summary of Role:

You will execute in vivo studies, analyze, and present data. You will gain and provide technical and scientific in vivo pharmacology expertise to advance drug discovery programs from target identification/validationto IND enabling activities. You will interact and collaborate effectively in a multi-functional dynamic team environment.

Responsibilities:

  • Setup and executein vivostudies to validate targets, test novel drugs (small and large molecules), and combination strategies with a focus on oncology/immuno-oncology models (including syngeneic tumor models, xenograft models, models using transgenic lines, GEMMs etc) .

  • Generate graphs, statistics, and figures for in vivo data

  • Document data generated as a report in electronic notebook.

  • Present study findings within IVP and/or at cross-functional team meetings

  • Comply with IACUC and AALAC regulations.

Education and Experience:

  • Bachelor’s degree with 5+ years or Master’s degree with 2-5 years’ experience working with animals in academic or industry setting and/or translational drug discovery experience.

  • Hands on expertise in broadin vivopharmacology skills (dosing via different routes e.g. I.P, I.V, PO etc, tissue/blood collection).

  • Experience with syngeneic and xenograft tumor models is highly preferred.

  • Experience with data capturing and analysis software is preferred (i.e. electronic notebook, StudyLog, PRISM, Excel).

  • Experience in ex vivo assays like FACS is a plus.

  • Excellent interpersonal and communication skills to interact effectively with internal and external colleagues fostering a collaborative workplace environment.

  • Comfortable working in a fast-paced environment while supporting project timelines.

BMSONCRD, BMSDDTMRCA

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.

Physical presence at the BMS worksite or physical presence in the field is an essential job function of this role which the Company deems critical to collaboration, innovation, productivity, employee well-being and engagement, and enhances the Company culture.

To protect the safety of our workforce, customers, patients and communities, the policy of the Company requires all employees and workers in the U.S. and Puerto Rico to be fully vaccinated against COVID-19, unless they have received an exception based on an approved request for a medical or religious reasonable accommodation. Therefore, all BMS applicants seeking a role located in the U.S. and Puerto Rico must confirm that they have already received or are willing to receive the full COVID-19 vaccination by their start date as a qualification of the role and condition of employment. This requirement is subject to state and local law restrictions and may not be applicable to employees working in certain jurisdictions such as Montana. This requirement is also subject to discussions with collective bargaining representatives in the U.S.

Our company is committed to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace adjustments and ongoing support in their roles. Applicants can request an approval of accommodation prior to accepting a job offer. If you require reasonable accommodation in completing this application or if you are applying to a role based in the U.S. or Puerto Rico and you believe that you are unable to receive a COVID-19 vaccine due to a medical condition or sincerely held religious belief, during or any part of the recruitment process, please direct your inquiries to adastaffingsupport@bms.com. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.

Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.