Principal Scientist, Neuroscience
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 Neuroscience TRC is committed to development of transformational therapeutics for patients with neurodegenerative and neuromuscular diseases. We have built a network of external partnerships across multiple treatment modalities (small molecules, biologics and RNA targeting) that leverage our leadership in protein homeostasis and inflammation to attack neurological diseases. Internal research focuses on protein homeostasis by direct and ligand directed degradation, neuroinflammation and remyelination.
Areas of interest include, but are not limited to, the following approaches:
Disease modifying therapies for neurodegenerative, neuro-inflammatory and neuromuscular diseases; CNS targets that modulate protein homeostasis, protein clearance, inflammation and reduce or eliminate toxic protein production; Emerging technologies (RNA, DNA targeting, gene regulation, editing and replacement, vector optimization) that when matched to underlying disease genetics can deliver a precision medicine portfolio with a high probability of success to address unmet medical needs; Targets in orphan/rare neurological and neuromuscular diseases. AI/ML in target identification and neurology drug discovery; Translational tools and technologies such as neuroimaging and fluid biomarkers to track neurodegenerative disease; Novel blood brain-barrier delivery technologies.
This opening for a Principal Scientist is for a laboratory-based, integral member of the Neuroscience Thematic Research Center (TRC) who can use their neuroimmunology expertise to lead research projects as well as contribute to the clinical transition of new drug candidates for a broad range of neurodegenerative indications. The successful applicant will leverage their experience in neuroinflammation/immunology and in vitro/ex vivo studies with sophisticated lab techniques for biomarker detection and assessment to work collaboratively across disciplines (eg, in vivo) to pharmacologically characterize target engagement and efficacy in relevant models. This position offers great potential for continued growth with exposure to all aspects of disease modelling and drug development and as such, in vivo experience would be considered highly advantageous. The Senior Principal Scientist will also be in a position to offer training and oversight to junior team members while participating in project teams and contributing to regulatory submissions.
Implementation and validation of assay systems in ex vivo samples and/or cell types to screen and characterize the pharmacological responses to modulation with small molecules, antibodies etc.
Development of assays with readouts that are translationally-relevant to the neurodegenerative indications
Ability to develop assays for in vivo target engagement assessment
Identification and assessment of potential new Neuroscience-focused targets
Ability to create new research plans and to present at project team and departmental meetings
Ability to actively participate in and oversee outsourced projects/collaborations
Creation and interpretation of scientific documents including study protocols and study reports suitable for regulatory submission
Mentorship of junior team members
Generate, record and report raw data and interpret to refine the next steps
Ensure the proper documentation of all data in electronic notebooks
Ability to analyze complex data using software tools and appropriate statistical analyses and make concise graphic presentations.
Other responsibilities as assigned
8+ years of academic and / or industry experience
6+ years of academic and / or industry experience
Ph.D. or equivalent advanced degree in the Life Sciences
4+ years of academic and / or industry experience
Ph.D. in Biology, Neuroscience, Immunology (or similar field) and 5+ years of post-doctoral research experience, preferably with at least 5+ years of industry experience
Supervisory experience is considered advantageous
Flow cytometry and application of neuroimmunology expertise
Demonstrated history of applying a broad variety of in vitro/ex vivo laboratory skills to drive progress in a variety of projects
Experience with iPSC microglia/astrocytes
Data interpretation and application to the design and optimization of follow-on studies
Capable of working within a fast-paced team environment that contributes to multiple projects at any given time
Ability to work independently as well as collaboratively, both within the immediate research team and across company sites and functions
Excellent organizational, record keeping, plus oral and written communication skills
Motivated and detail-oriented with a strong interest in driving productivity in clinically-directed research
Skilled in using standard software as well as specialist equipment, graphing and statistical analysis software
Positively contribute to a work environment that fosters professionalism, mutual respect, teamwork, output and collaboration
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.
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