Associate Director, Neuroscience, Clinical Biomarker, Late Phases, Translational Medicine

Bristol Myers SquibbSan Diego, CA
6d$186,110 - $259,344Hybrid

About The Position

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. 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. Translational Development Overview Translational Development is part of the Global Research 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 Development drives strategy across core therapeutic areas at BMS including hematology, oncology, immunology, cardiovascular and neuroscience. 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.

Requirements

  • PhD or MD/PhD in neuroscience with 7+ years of translational medicine experience
  • 5+ years of late-stage clinical biomarker experience in biotech/pharma
  • Recognized expertise in translational biomarkers in neuroscience space
  • Deep training and education in Neuroscience required
  • Experience in late-stage drug development and activities required for and related to clinical trial initiation, maintenance and completion
  • Strong verbal and written communication skills
  • Experience in interacting with CROs and TLs to manage projects and timelines
  • Proven scientific/leadership expertise (working in teams, mentoring people, managing projects)
  • Accountable for timelines and deliverables
  • Prioritizes risks and implements contingency plans
  • Communicates regularly; prepares and delivers presentations within the department, to governance and senior leadership bodies, and externally as requested
  • Recognizes cross-functional issues and communicates within the larger organization.
  • Provides expert guidance to multi-disciplinary teams and senior management.
  • Has a track record of delivering results, driving continuous improvements, and building effective cross-functional networks.
  • Ability to prioritize and manage time efficiently
  • Accurate and detailed record keeping
  • Excellent organizational skills

Responsibilities

  • Designs and implements program-specific late development 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 partnering with Translational Sciences colleagues when applicable
  • 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 applying external knowledge to internal research programs as appropriate and acts as a subject-matter expert within the team to critically evaluate the literature regarding the asset and disease biology
  • 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

Benefits

  • Health Coverage: Medical, pharmacy, dental, and vision care.
  • Wellbeing Support: Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).
  • Financial Well-being and Protection: 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.
  • Work-life benefits include: Paid Time Off US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees) Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays Based on eligibility, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day. All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown.
  • Eligibility Disclosure: The summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program.

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What This Job Offers

Job Type

Full-time

Career Level

Mid Level

Education Level

Ph.D. or professional degree

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