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Study Director Community Lead

Trabajo disponible en: 08001, Barcelona, Cataluna, España
Empresa: Novartis Farmacéutica
Tiempo completo puesto
Publicado en 2026-02-07
Especializaciones laborales:
  • Servicios Médicos
    Administración de Salubridad
  • Gerencia
    Administración de Salubridad
Rango Salarial o Referencia de la Industria: 70000 - 90000 EUR Anual EUR 70000.00 90000.00 YEAR
Descripción del trabajo
Choose Location Choose Location### Summary Role type:
Hybrid Woking, #LI-Hybrid

Location:

Barcelona, Spain  Relocation Support:
This role is based in Barcelona, Spain. Novartis is unable to offer relocation support: please only apply if accessible.
Lead a global community of Study Leaders from our Barcelona hub to deliver high quality clinical trials—faster, smarter, together. You’ll coach and enable Study Leaders across Novartis hubs, strengthen standards and ways of working, and build a trusted, resilient, high performing community. You will guide study planning and decision making, remove obstacles, and drive timely, quality, and compliant execution of Global Clinical Operations (GCO) supported studies.

We’re looking for someone with significant experience leading complex global trials, proven people leadership and stakeholder management, and strength in operational planning and risk/issue management. Join us to develop talent, scale best practices, and make a measurable impact for patients.### About the Role
** KEY RESPONSIBILITIES
*** Lead a community of Study Leaders, fostering collaboration, trust, and shared learning across end-to-end study activities.
* Oversee the execution and delivery of a diverse clinical study portfolio within the assigned community by trial type.
* Drive continuous improvement and innovation in trial operations to elevate study efficiency, quality, and outcomes.
* Coach and develop Study Leaders, strengthening capabilities and therapeutic understanding.
* Optimize resource allocation by assessing workload, priorities, and community needs in partnership with Study & Site Operations (SSO) leadership.
* Ensure robust risk management, inspection readiness, and adherence to global standards and regulatory expectations.
* Build strong cross‑functional partnerships with global teams and vendors to support seamless study execution.
** KEY PERFORMANCE INDICATORS
*** Timely, efficient, and high-quality delivery of assigned studies and study-related activities within budget, and in compliance with quality standards
* Proactive, iterative operational planning with effective contingencies and embedded risk management mindset in the Clinical Trial Team (CTT)
* Sustainable and measurable improvements (Speed, Cost, Quality) of type of clinical trials with the assigned community
* Team's satisfaction, retention and development.
** ESSENTIAL REQUIREMENTS
*** Bachelor’s degree in life sciences, healthcare, or a clinically relevant discipline; an advanced degree is strongly preferred.
* At least eight years of recent experience in clinical research or drug development across Phase I–IV studies.
* Minimum five years of experience delivering medium to highly complex clinical studies in a global matrix environment.
* At least five years of people leadership experience, ideally managing teams across multiple countries.
* At least 5 years of recent contribution to and accomplishment in all aspects of conducting clinical studies of medium to highly complexity and of high priority (e.g., planning, executing, reporting, and publishing) in a global/matrix environment in pharmaceutical industry or a contract research organization, including expert knowledge of international standards International Council for Harmonization  Good Clinical Practice (ICH GCP), health authorities (Food & Drug Administration / European Medicines Agency  (FDA/EMA)), local/National Health Authorities regulations
* Proven ability to lead virtual teams and build high‑performing, capability‑driven groups.
* Demonstrated experience developing effective relationships with internal and external partners.
* Strong project leadership, planning, and problem‑solving skills, with a track record of driving process improvements.
** LANGUAGE
* ** Fluent English communication skills, with strong ability to present complex information clearly.
** You’ll receive:
** You can find everything you need to know about our benefits and rewards in the Novartis Life Handbook.

** Commitment to Diversity and Inclusion:
** Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.

** Join our Novartis Network:
** If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here:
** Why Novartis:
**** Benefits and Rewards:
** Learn about all the ways we’ll help you thrive personally and professionally.

Spain

REQ-### Study Director Community LeadREQ-### Study Director Community Lead
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