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Bristol-Myers Squibb

Translational Medicine Sr. Principal Scientist Neurology

Bristol-Myers Squibb, San Diego, California, United States, 92189


Translational Medicine Sr. Principal Scientist NeurologyLocations:

San Diego – CA – US, Brisbane – CA – US, Princeton – NJ – US, Summit East – NJ – US, Cambridge Crossing – MA – USTime Type:

Full timePosted On:

Posted 2 Days AgoJob Requisition ID:

RWorking with UsChallenging. 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.Summary/ScopeReporting to Senior Scientific Director Translational Medicine, the TM Sr. Principal Scientist will be part of the late–stage TM group. The individual will be responsible for TM and clinical biomarker activities to support drug development programs in multiple diseases in neurology and neuropsychiatry.Responsibilities will include, but are not limited to:Designs and implements program–specific biomarker/translational plans, responsible for aiding in creation of clinical protocols, SAPs, SOWs, lab manual, and interfacing with CRO for execution of services, in conjunction with Biospecimen Operations and Procurement.Determines appropriate assays and vendors for clinical biomarkers, and manages outsourcing of biomarker assay development and validation.Manages clinical biomarker data delivery and analysis and associated timelines by working with relevant internal functions and CROs.Prepares and delivers internal and external translational/biomarker presentations.Maintains timelines for biomarker data–related publication through interaction with Medical Communications and Publication team as needed.Keeps up–to–date on relevant scientific/technical literature in order to apply external knowledge to internal research programs as appropriate.Works with TM laboratory scientists and academic TLs to address nonclinical translational questions.Participates in post–hoc biomarker analysis and publication efforts.Supports regulatory submissions and regulatory interactions as needed.Skills/Knowledge Required:Understanding of late–stage drug development.Experience in activities required for and related to clinical trial initiation, maintenance, and completion.Experience in interacting with CROs and TLs to manage projects and timelines.Proven scientific/leadership expertise.Accountable for timelines and deliverables.Strong verbal and written communication skills.Excellent organizational skills.Basic Qualifications:Bachelor's Degree with 10+ years of academic and/or industry experience, orMaster's Degree with 8+ years of academic and/or industry experience, orPh.D. or equivalent advanced degree in the Life Sciences with 6+ years of academic and/or industry experience.2+ years of leadership experience.Preferred Qualifications:Ph.D. in neuroscience or related field with 8+ years of academic/biotech experience.Minimum 3 years of clinical biomarker experience.The starting compensation for this job is a range from $159,000 – $200,000, plus incentive cash and stock opportunities (based on eligibility).Behavioral Competencies:Champions change, leads courageously, networking, provides directions, thinks strategically.

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