Senior Scientist Translational Research - Molecular Based Assays
Bristol Myers SquibbAbout the role
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: careers.bms.com/working-with-us.
The successful candidate for the Sr. Scientist position will be a highly motivated and collaborative scientist responsible for developing, validating and implementing molecular based assays to support exploratory translational research in the clinical setting within the Translational Research department in the Cancer-Oncology and Cellular Therapy Thematic Research Center.
The candidate will collaborate closely with the Biomarker Lead to establish assays in alignment with the program's translational strategy. The individual will provide end to end support of the clinical assays lifecycle which may include liaising with external labs, establishing data specifications, checking quality of data generated, and supporting interpretation of the results.
Position Responsibilities
In the role as a Senior Scientist within the Translational Research team, the ideal candidate:
Applies scientific and / or technical skills and functional knowledge to conduct experiments / research / studies in assigned area
Adapts standard methods and techniques by applying breadth of knowledge and prior work experience
Makes decisions that impact entire work group / project team
Contributes to initiatives related to continuous improvement or development of new approaches / technologies
Starts to develop and implement approaches to new technology and take calculated risks
Leads discussions and makes presentations in multidisciplinary meetings, logically presenting information to convey clear, key messages
Is expected to explain, persuade, and build alignment for situations
May represent department or function on program / project team or sub-team
Serve as a subject matter expert in molecular-based assays, collaborate with project teams and biomarker leads on the fit for purpose design and implementation plan of assays to address key translational questions in early phase clinical trials
Provide technical guidance on assay selection, design, optimization, qualification and/or validation, and implementation
Lead the development and analytical validation of molecular based assays internally and or at external vendors to support our CICT TRC clinical trials globally
Troubleshoot assay data and technical issues effectively and efficiently with internal teams and external partners
Apply molecular biology, and biochemical laboratory techniques with efficiency, accuracy, and attention to detail; conduct data analysis, report and represent results independently in collaborative environment to the team and relevant stakeholders
Lead and collaborate with internal cross-functional teams and external partners to oversee assays at contract research organizations
Review and author technical documents including protocols, validation reports, publications, regulatory documents, etc.
Basic Qualifications:
Bachelor’s Degree
7+ years of academic and / or industry experience
Or
Master’s Degree
5+ years of academic and / or industry experience
Or
Ph.D. or equivalent advanced degree in the Life Sciences
2+ of academic and / or industry experience
Preferred Qualifications:
Requires thorough knowledge of varied aspects or a single specialized aspect of own discipline and developed knowledge of other related disciplines
Is proficient in scientific / technical writing (e.g., regulatory documents, protocols)<
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