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Bristol Myers Squibb Company

2024-09-21 12:35:48

Job location Summit, New Jersey, United States

Job type: fulltime

Job industry: Science & Technology

Job description

Working with Us
Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible.

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. Read more: .

Translational Medicine at BMS

Translational Medicine is part of the Global Research and Early Development organization in BMS and leads late stage clinical, pharmacological and translational research and development activities for the pipeline and supports late-stage portfolio for regulatory, translational development and life cycle management. Translational Medicine Hematology drives strategy for multiple disease areas of interest including Multiple Myeloma, Lymphoma, CLL, AML, MDS, anemias and other hematological malignancies. This group integrates laboratory science, clinical trial/biomarkers and asset development as well as disease research to maximize the potential of BMS current and future therapeutics.

Summary

Working within Translational Medicine Team, the candidate will be part of the translational group based in Summit NJ and will contribute to/manage the scientific and preclinical laboratory component of late-stage hematology programs (phase 2 and beyond). Key responsibilities of this role are to lead from the bench for the preclinical support of asset programs through mechanism of action-based studies, differentiation from standard of care molecules, combination rationale and resistance mechanisms. He/She will work with translational scientists, disease leaders within translational medicine and thematic research centers in early development within the company.

Responsibilities

  • Conduct preclinical/laboratory research to support late-stage BMS compounds. Contribute to achieving the annual goals and objectives of the Hematology Translational Medicine group, including internal and external collaborations and compound-specific plans.
  • Responsible for delivering data in support of translational strategies including biomarkers, patient selection hypotheses, dose and schedule, combination strategies, resistance mechanisms, drug differentiation and therapeutic target identification/validation
  • Interfaces with other research scientists within and outside of the Heme TMDT group to ensure seamless flow of information for assets which are entering the remit of translational medicine
  • Communicates regularly and prepares and makes presentations within the department
The successful candidate will have:
  • Extensive experience in handling and maintaining mammalian cells.
  • Research experience in the field of molecular/cell/cancer biology, translational research, or another relevant field
  • Solid scientific background in understanding and performing cell-based assays and readouts
  • Capable of critical and creative thinking across various disciplines. Proven problem-solving skills in research, including experience with standard in vitro assays, assay development, optimization, and troubleshooting
  • Ability to multitask and effectively collaborate with a diverse team of scientists to achieve results and meet stakeholder needs
  • Strong verbal and written communication skills with experience in developing written documents such as primary manuscripts/publications
Basic Qualifications:
  • Bachelor's Degree with 5+ years of academic and / or industry experience
Or
  • Master's Degree with 3+ years of academic and / or industry experience
Or
  • Ph.D. or equivalent advanced degree in the Life Sciences
Preferred Qualifications:
  • In-depth understanding of cancer biology (hematology a plus) and evolving technologies
  • Extensive hands-on experience with molecular and cellular biology techniques and cell-based assays, including but not limited to: DNA/RNA purification, qPCR, flow cytometry, Western blotting, capillary Western blotting, InCucyte, MSD/ELISA, RNAi, CRISPR/Cas9-mediated gene editing, and drug combination assays
  • Experience with next-generation sequencing and single-cell sequencing technologies is a plus
  • Experience in isolating Monocytes, T-cells and NK cells from PBMCs is a plus
  • Strong ability to troubleshoot and optimize novel methods and protocols
  • Good understanding of drug development process in an industry setting with clear examples of success
  • Understanding of late-stage drug and translational development process
  • Ability to work with disease teams/experts to develop preclinical strategies to support clinical development and life cycle management
  • Mindset focused on continuous improvement, actively seeking opportunities to enhance lab efficiency and safety
If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.

Uniquely Interesting Work, Life-changing Careers
With a single vision as inspiring as Transforming patients' lives through science , every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.

On-site Protocol

BMS has a diverse occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:

Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.

BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to . Visit eeo -accessibility to access our complete Equal Employment Opportunity statement.

BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.

BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.

If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information:

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

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