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    Senior Director, Biostatistics - Princeton, NJ, United States - Bristol-Myers Squibb

    Bristol-Myers Squibb
    Bristol-Myers Squibb Princeton, NJ, United States

    1 week ago

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    Description
    Working 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.

    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:
    individual leads the Biostatistics function In Neuroscience and/or Cardiovascular therapeutic areas of BMS and responsible for providing statistical input to development strategies, and effective implementation plans to support product development or market access objectives in a global organization. The Senior Director provides expertise and guidance in collaboration with cross-functional groups broadly across the organization in establishing study design and analyses and strategy, and institutes best practices with regards to planning, execution, interpretation and regulatory submission of clinical projects and studies. Provides guidance and management to statisticians to ensure high quality and timely deliverables. Manages resources, sets priorities, and ensures consistency and adherence to standards therein.

    Key ResponsibilitiesManages a functional or project budget, and has authority to allocate company resources according to the development needs of multiple compounds/indications within therapeutic areas, and sets prioritiesDirects and guides statisticians to ensure high quality and timely deliverablesCompliant with BMS processes and SOPs, adherence to global and project standardsEnsures consistency and adherence to standards across therapeutic areas and projectsKey contributor to Clinical Development Plans, submissions, and post-submission strategies/preparation/ defense as neededRepresents the company in interfaces with regulatory agencies globallyDrives strategy for processes improvement, contributes to new departmental SOPs, and provides training on statistical topics and departmental SOPsParticipates in industry-wide technical discussions, and represents company in professional societiesEncourages new ideas, innovation, and continuous improvements across GBDSAnticipates potential issues and takes preventive measures; identifies and oversees the resolution for the teamEffectively engages as a matrix team member on high level development teams and acts as a scientific and strategic partner and establishes new collaborations with cross-functional areas; maintains existing stakeholder collaborationsContributes to functional goal setting and forward planningEffectively communicates the GBDS Mission and Vision in a fashion that generates pride, excitement and commitment within GBDSEnables a culture of inclusiveness, respect for diversity, compliance with process and allows for the questioning and challenging of others in a respectful and constructive mannerApplicable to people managersEffectively engages as an employee advocate and management coach/mentor to team members - both internally and externallyProvides leadership to empower and develop the teamProvides guidance to employee's development plans and carries out performance review and feedback.

    develops performance metrics for staffQualifications & ExperiencePhD or MS (12+ years' experience) in statistics or biostatistics or related scientific field with clinical trials, drug development, pharmaceutical industry or healthcare experienceProficiency in scientific computing/programming (SAS, R or Python) and implementation of advanced statistical analysis, data manipulation, graphing & simulationExcellent interpersonal, communication, writing and organizational skillsDemonstrate expertise in applying knowledge of general and cutting edge statistical / clinical trials methodology to solve complex statistical problems in the clinical development area and ensure alignment with regulatory agencies and industry standardsExtensive experience in preparing and participating in global regulatory agency interactionsDemonstrate excellent collaboration, organizational/ leadership abilities, and interpersonal skillsDemonstrate development of resourcing strategies and recruiting practices, working with senior leaders to define positions and organizational structure, and anticipating future requirements and specialty areasAt least 5 years management (direct or matrix) experience is preferred (for people manager position only)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 CareersWith 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 ProtocolPhysical presence at the BMS worksite or physical presence in the field is a necessary job function of this role, which the Company deems critical to collaboration, innovation, productivity, employee well-being and engagement, and it enhances the Company culture.

    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 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.

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



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