Global Program Leader (1 of 4)

Janssen Research and Development, L.L.C., a member of Johnson and Johnson's Family of Companies, is recruiting for a Global Program Leader. This position can be located in Spring House, PA; Titusville, NJ; Raritan, NJ; Beerse, Belgium; High Wycombe, United Kingdom; Leiden, Netherlands; or Breda, Netherlands. Remote locations within North America and Europe may be considered. At the Janssen Pharmaceutical Companies of Johnson & Johnson, what matters most is helping people live full and healthy lives. We focus on treating, curing and preventing some of the most devastating and complex diseases of our time. And we pursue the most promising science, wherever it might be found. Janssen Research & Development, LLC discovers and develops innovative medical solutions to address important unmet medical needs in oncology, immunology, neuroscience, infectious diseases and vaccines, cardiovascular and metabolism, and pulmonary hypertension. Please visit for more information. The Global Program Leader (GPL) will have primary global accountability for Global Development (GD) program (IDP) level operational delivery with regard to time, quality and budget. This individual will be a member of a Therapeutic Area (TA) Clinical Team, or an equivalent cross-functional strategic team, and will provide operational expertise and input into the strategic planning and execution of a global clinical development program or group of clinical trials. Key accountabilities include: robust strategic operational planning; ensuring full integration of GD resources and budget to the assigned program(s); obtaining alignment on outsourcing strategy; resource allocation; overseeing matrix team assignments; and ensuring deliverables are met within agreed timelines, with high quality and meeting Janssen's procedural, International Conference on Harmonization-Good Clinical Practice (ICH-GCP) and regulatory requirements. Principal Responsibilities: * Proactive risk management and mitigation planning from the start of a clinical development program (IDP) until closure. * Act as the single point of accountability within GD at the global program level and be accountable for leading high performing teams. * Serve as the key contact for the Janssen Therapeutic Area Clinical Leaders/other Janssen companies or external development partner companies and represent GD on senior leadership/project teams as appropriate. * Ensure alignment on business goals and TA/program objectives and lead the GD cross- functional matrix teams. Lead a team of Global Trial Leaders (GTLs) to ensure consistencies across trials, and leverage synergies and innovative approaches across a program. Oversee GD resourcing and be a key contact for the (Clinical) Project Management Lead for the duration of the program. * Directly supervise a group of GTLs and be accountable for the management and development of staff within scope of responsibility while fostering a diverse work force that works seamlessly in a highly matrixed environment. * Single point of accountability for providing strategic operational input to the clinical development plan, building the strategic operational plan and budget for GD deliverables and milestones, and provide global leadership to the execution to plan and/or define risk mitigation strategies and ensure implementation within GD. * Create and gain endorsement of the global strategic operational plan (IDP/program level), inclusive of the sourcing strategy, supplier selection strategy and aligned country selection plan. Ensure an integrated data plan for external data streams is available and endorsed. * Oversee clinical trial budget forecasting and management. * Lead Contract Research Organization (CRO) selection, ensure scope of work is defined and define deliverables, turnaround times, and quality and performance levels for new sourcing needs. Qualifications * A minimum of a Bachelor's or equivalent University degree is required, preferably in a scientific discipline (e.g. Biology, Chemistry, Biochemistry, Nursing, Pharmacy). Advanced degree (e.g. Master's, MBA, MD, PhD) is preferred. * A minimum of 10 years of experience in clinical operations within the Pharmaceutical industry or Contract Research Organization (CRO) is required. * Experience in any of the following Therapeutic Areas preferred: Oncology, Neuroscience, Immunology, Cardiovascular, Metabolism, Infectious Diseases, Vaccines. * Global clinical operational experience (Phase 1-3B) or clinical project management experience is required. * Experience with Early Development clinical trials preferred. * Experience managing external stakeholders/CRO programs is required. * Knowledge of global regulatory, quality and logistical aspects of global and local clinical trial conduct and oversight is required. * Experience leading a global R&D registration program is preferred. * CRO management experience is preferred. * People management experience is strongly preferred. * Must have excellent people leader