REQ-10043365
Mar 05, 2025
Canadá

Resumen

~Supervisa la ejecución e interpretación de investigaciones de ensayos clínicos, actividades de recopilación de datos y operaciones clínicas. Establece y aprueba métodos científicos para el diseño e implementación de protocolos clínicos, sistemas de recopilación de datos e informes finales. Ayuda en investigaciones clínicas nuevas y constantes y en ensayos clínicos y asegura la eficiencia y el oportuno procesamiento de acuerdos de confidencialidad y acuerdos clínicos. Superv. el cumplim. de los protoc. y determ. la terminación de los estudios. Gestiona archivos clínicos y reglamentarios y mantiene el inventario clínico previsto para la distribución a sitios de investigación. Puede interactuar con sitios de investigación, consultores clínicos, Organizaciones de Investigación de Contratos y otros proveedores. Selecciona, desarrolla y evalúa personal para asegurar la operación eficiente de la función.

About the Role

Key Responsibilities:

  • Provide clinical development and indication expertise specific to the country/cluster.
  • Validate study designs, contribute to the start-up phase, provide robust training to clinical operations teams and support recruitment and trial awareness.
  • Offer clinical/medical expertise for IRB/EC interactions and informed consent forms.
  • Interact with external experts, regulatory authorities, and patient advocacy groups.
  • Leverage innovation in clinical trial planning and recruitment strategies.
  • Support internal stakeholders and decision boards regarding clinical trials.
  • Review and resolve trial-related scientific/clinical/medical issues and support protocol deviations.

Essential Requirements:

  • Scientific degree M.D., Ph.D., or Pharm.D. (M.D. highly desirable) - Subspecialty training desirable
  • 3 years of clinical development experience in the pharmaceutical industry or clinical practice.
  • Ability to manage a study from the scientific/medical/clinical perspective, and a demonstrated capability to problem solve and mediate complex scientific/clinical/medical/operational issues.
  • Ability to lead effectively by communicating well, motivating a cross-functional team, and handling and delegating responsibilities.
  • Agility to move quickly across different therapeutic areas and indications.
  • Demonstrated problem-solving skills and comfort with complexity.
  • Ability to prepare and deliver high quality presentations.

Desirable Requirements:

  • Sound understanding of the overall clinical development process, and ICH/GCP principles.
  • Speaks and writes English, French desirable

Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture

Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network

Benefits and Rewards: Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards

Development
Innovative Medicines
Canadá
Montreal
Research & Development
Full time
Regular
No
A female Novartis scientist wearing a white lab coat and glasses, smiles in front of laboratory equipment.
REQ-10043365

Clinical Research Medical Advisor

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