Clinical Trial Excellence Project Manager
hace 1 día
Sabadell
ppSalary Range: $0.00 - $0.00 /ppJob Description Summary The Clinical Trial Excellence (CTE) Project Manager supports the delivery of operational excellence in trial management at Novartis, as defined by the CTE Head. Focusing on the Study Leader (SL) role, and associated ways of working, governance, collaboration, inspection readiness, and trial execution performance. This global role is part of the CTE organization and supports the CTE Head and CTE Lead in translating the enterprise trial management excellence strategy into practical, scalable standards and solutions for SLs. The CTE Lead drives harmonized SL execution practices across programs and trials, strengthens SL role clarity and capabilities, and enables Study Leadership to operate with greater trial leadership consistency, quality, agility, efficiency and accountability. The CTE PM collaborates with the CTE Lead and CTE to support an effective, measurable, Study Leadership excellence model that is aligned with organizational priorities, latest regulatory requirements, and industry best practices. The role integrates business, quality, risk, digital, and operational needs for SLs, including proactive risk management, data quality, TMF documentation, inspection readiness, and effective trial-level oversight and decision-making. The CTE PM establishes, deploys, and continuously improves guidance, playbooks, training, metrics, dashboards, and tools for the assigned area (per CTE Head). The role drives execution through matrix leadership, cross-functional collaboration, and targeted initiatives that simplify workflows, embed quality by design, and support adoption of digital and AI-enabled solutions. /ppJob Description #LI-Hybrid Relocation Support: This role is based in Barcelona Gran Via, Spain. Novartis is unable to offer relocation support: please only apply if accessible. /ppAbout the Role Help shape the future of clinical trial delivery at Novartis. As a Clinical Trial Excellence Project Manager, you will play a pivotal role in advancing Study Leadership excellence across our global clinical development organization. Working at the intersection of trial execution, quality, innovation, and operational excellence, you will help create scalable solutions, strengthen trial leadership capabilities, and drive continuous improvement in how clinical studies are delivered. This is a unique opportunity to influence global ways of working, champion digital and AI-enabled innovations, and partner with diverse stakeholders to improve quality, agility, inspection readiness, and patient-focused outcomes across our clinical trial portfolio. /ph3Key Responsibilities /h3ulliDrive implementation of Study Leadership excellence standards across global clinical trial programs and study archetypes. /liliDevelop and enhance guidance, playbooks, tools, and best practices that strengthen trial leadership effectiveness. /liliLead cross-functional initiatives that improve trial execution quality, consistency, agility, and operational oversight. /liliPartner with Study Leaders and stakeholders to strengthen governance, decision‑making, and inspection readiness. /liliCreate metrics, dashboards, and insights that measure Study Leadership performance and continuous improvement. /liliDesign and deliver training, communications, and communities of practice that support capability development. /liliPromote quality by design, proactive risk management, and Trial Master File documentation excellence. /liliEvaluate industry trends and emerging practices to identify opportunities for innovation and operational improvements. /liliCoordinate workshops, leadership forums, and strategic communications that drive alignment and adoption. /liliLeverage digital tools, analytics, Copilot, and artificial intelligence solutions to enhance trial delivery outcomes. /li /ulh3Essential Requirements /h3ulliBachelor's degree in Life Sciences, Healthcare, or a related scientific discipline. /liliMinimum five years of clinical operations, clinical research, or clinical trial management experience. /liliExperience leading or matrix‑leading cross‑functional teams, initiatives, or complex trial delivery activities. /liliStrong understanding of drug development, clinical trial execution, and Good Clinical Practice requirements. /liliProven ability to drive operational improvement, process simplification, and continuous improvement initiatives. /liliDemonstrated success translating strategic objectives into measurable plans, deliverables, and adoption strategies. /liliExcellent stakeholder management, communication, presentation, and collaboration skills in global matrix environments. /liliExperience using clinical systems, data analytics, dashboards, digital tools, or artificial intelligence‑enabled solutions. /li /ulh3Benefits Rewards /h3ulliThe base salary offered is determined based on gender‑neutral objectives, such as relevant skills, competencies and experience in accordance with the Novartis pay setting policy and upon joining Novartis will be reviewed periodically. /liliIn addition to your base salary, you may be eligible for a performance‑based bonus depending on certain performance parameters. /liliThe rewards of being part of our team go far beyond base pay and incentives. /liliWe also offer a variety of competitive benefits in kind to help you thrive personally and professionally, such as insurance plans, retirement plans, wellbeing resources and global recognition programs. /liliIn addition, we provide flexible and hybrid working options, where possible, and minimum 14 weeks paid parental leave. /liliPay equity is a fundamental principle of our employment policy and reflects our commitment to create a diverse, equitable and inclusive environment that treats all employees with dignity and respect, as outlined in our Code of Ethics. /liliRead our brochure to learn more about our global total rewards offering: /liliNote: Benefits and compensation may vary by country and are subject to local legal requirements, including provisions of collective bargaining agreements where applicable. /liliA full overview of your compensation package, including any relevant collective bargaining agreement details applicable to your role based on your employment location and Novartis employer entity, will be communicated separately to you during the application process. /li /ulpSkills Desired Clinical Research, Clinical Trials, Data Management, Global Project Management, Health Sciences Improving the lives of people living with disease takes more than innovative science. It takes a focus on the needs of people and a community committed to meeting them. It takes a team of people like you. Working together. Learning together. Thriving together. Discover how you can join us in changing people’s lives. /ppIn the context of China Cross‑Border Data Transfer (CBDT) policy, if you need to apply for a position in China, please go to the local Recruiting System TaleNov. /p /p #J-18808-Ljbffr
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