REQ-10056412
8月 08, 2025
Brazil

摘要

~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

  • Validate study designs and assess trial feasibility based on clinical practice and competitive analysis.
  • Drive fast and high-quality trial site start-up through expert input during planning phases.
  • Provide clinical expertise for IRB/EC interactions and informed consent content.
  • Develop trial plans that address recruitment challenges and ensure data quality.
  • Deliver robust training on indications, compounds, and protocols to internal and external stakeholders.
  • Lead clinical recruitment strategies using physician insights and patient engagement.
  • Support regulatory inspections and audits with scientific and clinical expertise.
  • Ensure adherence to safety standards and provide medical input on adverse events.

Essential Requirements

  • Advanced scientific degree (M.D. highly preferred; Ph.D. or Pharm.D. also considered).
  • Strong understanding of clinical development processes and ICH/GCP guidelines.
  • Minimum 3 years of experience in clinical development or clinical practice.
  • Proven ability to lead cross-functional teams and resolve complex clinical issues.
  • Excellent communication skills in English and the local language.
  • Ability to deliver high-quality presentations and adapt across therapeutic areas.

Desirable Requirements

  • Subspecialty training or experience with Real World Evidence (RWE).
  • Familiarity with innovative study designs and data sources such as registries or electronic health records.

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
Brazil
Santo Amaro
Research & Development
Full time
Regular
No
A female Novartis scientist wearing a white lab coat and glasses, smiles in front of laboratory equipment.
REQ-10056412

Clinical Research Medical Advisor

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