VP, Head of Portfolio Delivery Operations – Cross Therapeutic Area

工作内容

Janssen R&D is recruiting for a VP, Head of Portfolio Delivery Operations – Cross Therapeutic Area to be in San Francisco, CA; La Jolla, CA; Basel Switzerland; Beerse, Belgium, Leiden, Netherlands; OR High Wycombe, UK. This position provides overall leadership and direction to the Portfolio Delivery Operations organizations across the following therapeutic areas: Early Dev & Clinical Pharmacology, Neuroscience, CVMR, PAH, Infectious Diseases, and Vaccines (excluding Oncology and Immunology). This position will provide end to end clinical operations management and oversight to optimize the investment and performance of the JRD portfolio and accelerate the delivery of innovative medicines to patients. This position is also accountable for the alignment of processes, talent strategies and organizational strategies across the multiple PDO organizations to ensure a consistent and high quality operational approach across all therapeutic areas. In partnership with the Therapeutic Area and through the Clinical Development Teams, this position is accountable for executing the entire non-IMM/ONC clinical trial book of work from FIH studies, through registration and post-marketing commitments. Providing end-to-end accountability for the flawless execution of the non-IMM/ONC clinical trial portfolio, on budget, with the appropriate quality, and with industry-leading speed Consolidate country, site and patient insights to strengthen the design of clinical trial programs and protocols Champion the creation and implementation of new clinical trial models, including biomarker-driven studies, direct-to-patient models, embedding diversity in clinical trials, adaptive study execution, drug/device combination studies, etc. Provide leadership of the sourcing strategy, including both CRO support models, central and specialty labs, eCOA, IRT and all supporting external resources critical for the effective execution of oncology studies Develop industry-leading organizational capabilities and develop future operational leaders within the organization Manage a large, global organization and experience building, aligning and motivating global teams in a dynamic environment Develop and coordinate site relationships, including new site networks and expansion into emerging countries of interest Provide technical and clinical operational leadership for the 140-160 studies within the NS, Vx, ID, CVMR & PAH JRD portfolio inclusive of: Meeting or exceeding planned trial milestones Effectively managing study operational budgets / OOPs Coordinating resources and activities across both PDO and with other partner functions (GCO, IDAR, PMO. Etc.) Providing quality oversight of study execution and management Define and manage the sourcing strategy for the portfolio (finding the right balance between in-sourcing and outsourcing, including all specialty providers) Activate and nurture a culture of talent development within PDO across all TAs, creating a robust pipeline of future operational leaders. Foster harmony, effectiveness and efficiency amongst the GOHs with a continuous drive towards rapid issue resolution, customer satisfaction and TA partnership; developing strong working relationships with the other supporting clinical development functions Cultivate an environment of innovation through design and implementation of new clinical trial models and capabilities – ensure these learnings are infused across all TAs Monitor and manage overall performance from protocol design finalization to regulatory submission Efficient financial management of the PDO operating budget, including line management of assigned department heads and staff (~150). Decision making on optimal deployment and development of staff, in line with TA business priorities and talent – partnering with other functions to actively manage headcount demands from portfolio fluctuations/L&A deals Provide clinical trial insights into project and portfolio operational risks and discuss and rapidly implement mitigation actions Drive a culture of continuous improvement across PDO and R&D and a track record of delivering against financial continuous improvement targets Qualifications A minimum of a bachelor’s degree is required An Advanced degree (scientific or business orientation) is preferred A Minimum of 15 years of progressive pharmaceutical development experience with at least 10 years experience in the pharmaceutical R&D Clinical Operations environment is required Global clinical operations experience across multiple Disease Areas and experience across early development to registrational studies Proven track record of delivering portfolio milestones using innovative approaches to trial execution, site relationships and patient engagement Global and diversity-oriented people management experience including line management and matrix management. Experience with working in or with global and multidisciplinary R&D teams. Change management/leadership experience in driving complex transformation efforts. Excellent interpersonal and communication skills. Demonstrated ability to influence decision making at all levels. Ability to develop strong partnerships in a matrix environment. Fostering a culture of accountability and empowering others. Driving a CREDO-based culture, including a diverse and inclusive work environment. Demonstrated inspirational leadership and ability to set a vision for the future; a drive for delivering and exceeding business results. Proven ability to act as a change agent and adapt to rapidly changing organizational and business issues. Primary Location United States-California-San Francisco- Other Locations Europe/Middle East/Africa-Switzerland, Europe/Middle East/Africa-Belgium-Antwerp-Beerse, Europe/Middle East/Africa-Netherlands-South Holland-Leiden, Europe/Middle East/Africa-United Kingdom-England-High Wycombe, North America-United States-California-La Jolla Organization Janssen Research & Development, LLC (6084) Job Function R&D Requisition ID 2206005502W