\\n Bei Bristol Myers Squibb lassen wir uns von einer einzigen Vision inspirieren - die Ver\\xc3\\xa4nderung des Lebens von Patienten durch Wissenschaft. In den Bereichen Onkologie, H\\xc3\\xa4matologie, Immunologie und Herz-Kreislauf-Erkrankungen - und eine der vielf\\xc3\\xa4ltigsten und vielversprechendsten Pipelines der Branche - tr\\xc3\\xa4gt jeder unserer leidenschaftlichen Kollegen zu Innovationen bei, die bedeutende Ver\\xc3\\xa4nderungen vorantreiben. Wir verleihen jeder Therapie, f\\xc3\\xbcr die wir Pionierarbeit leisten, eine menschliche Note. Kommen Sie zu Bristol Myers Squibb und machen Sie einen Unterschied.

The Senior Manager, Innovation Strategy and Solutions Lead (Statistical programming&Technology) supports the framing, assessment, recommendation, and implementation of innovative strategies and solutions to bring efficiencies and automation to the clinical development process, under the direction of the Head Analysis Standards & Innovation. The incumbent will focus on innovative approaches to streamline processes and technology implementation with an ultimate goal of complete end to end solutioning. To that end, the job holder will work across Global Biometrics and Data Sciences departments, as well as cross functionally, including, but not limited to, Global Data Management & Centralized Monitoring, Clinical, Regulatory, Medical Writing, etc.

Responsibilities

• Support the framing, assessment, and recommendation of internal and external innovation initiatives, in collaboration with stakeholders across GBDS, to develop and implement more efficient and effective solutions for the development and maintenance of clinical development within biometrics and for the implementation of these solutions for use in clinical trials
• Provide strategic input to help drive projects to optimize the user experience across GBDS and with internal and external partners, fostering a continuous improvement and innovation culture with respect to the current and future solutions and related infrastructure
• Collaborate with GBDS teams to propose, develop, and drive forward innovative approaches to streamline implementation for GBDS as well as Global Drug Development
• Responsible for the scientific correctness and applicability of the solutions in support of the various clinical trial processes.
• Responsible for ensuring that processes and solutions are structured and governed in a manner that is well aligned with stakeholder processes in order to maximize efficiencies and value.
• Expertise on regulatory requirements (e.g. FDA, PMDA) pertaining to submitting and analyzing clinical trial data to regulatory authorities
• Bring to bear experience in data, digital, technology, and functional areas of biopharma to identify and prioritize new capability builds, in collaboration with business partners (e.g., IT, Procurement)
• Take ownership of internal and external teams to support ideas from conception to implementation
• Strategic partnering with leads, user community, and departmental/external stakeholders to identify innovation, automation, and continuous improvement opportunities. Proposes, evaluates and develops solutions and strategies that drive competitive advantage.
• Serves as a departmental resource in areas of technical expertise in the Clinical Data Interchange Standards Consortium (CDISC) standards related to the protocol development, statistical analysis, statistical programming and clinical study report authoring.
• Support development, implementation, maintenance, training, communications and continuous improvement of solutions supporting the GBDS\\xe2\\x80\\x99 portfolio of clinical trials.
• Maintains up to date knowledge of industry, functional and departmental processes, trends and technologies ensuring optimal implementation and adoption to support current and future needs.
• Ensures continued compliance with required company and departmental training, time reporting, and other business/operational processes as required for the position.
• Support design, development, deployment of innovation projects along with technology teams.
• Support innovation roadmap and strategic implementation and change management plans.

• Engages a network of internal and industry experts and leads the development of best practices and implementation of innovative solutions
• Actively engage as a member of industry organizations such as CDISC and PhUSE and work with industry experts to leverage and exchange knowledge and experience on regulations (e.g. FDA, PMDA) pertaining to the requirements for regulatory authorities

Degree Requirements

• Bachelors Degree in statistics, mathematics, computer science or other scientific field. Masters degree preferred.

Experience Requirements

• Minimum of 8 years in pharmaceutical industry.

Wir setzen uns auf der ganzen Welt leidenschaftlich daf\\xc3\\xbcr ein, das Leben von Patienten mit schweren Krankheiten zu beeinflussen. Unsere gemeinsamen Werte Leidenschaft, Innovation, Dringlichkeit, Verantwortlichkeit, Inklusion und Integrit\\xc3\\xa4t bef\\xc3\\xa4higen uns, unsere individuellen Talente und unterschiedlichen Perspektiven in einer integrativen Kultur einzusetzen und bringen das h\\xc3\\xb6chste Potenzial jedes unserer Kollegen hervor.

Bristol Myers Squibb wei\\xc3\\x9f um die Bedeutung von Balance und Flexibilit\\xc3\\xa4t im Arbeitsumfeld. Wir bieten daher eine Vielzahl von attraktiven Benefits, Dienstleistungen und Programmen an, die unseren Mitarbeitern die Ressourcen bieten, ihre Ziele sowohl bei der Arbeit als auch in ihrem Privatleben zu verfolgen.\\n \\n \\n \\n \\n \\n

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