Summary
En línea con la estrategia general del producto, el Asesor Médico es responsable de apoyar el diseño, la implementación y la ejecución de los planes de Asuntos Médicos para el Área de Terapia asignada, proporcionar información científica, ayudar a diseñar y organizar estudios clínicos, construir un diálogo educativo con los KOL y las partes interesadas reguladoras.
About the Role
Major Accountabilities
- Ensure that medical consultations are answered in a high quality, timely manner, and in accordance with applicable standards; establish standard response documents as appropriate for the most frequently asked questions.
- Provide medical/scientific input in the development and execution of clinical trials or activities related to clinical research, including initiation and supervision of clinical trials / clinical research in the respective therapeutic area. Support the country strategy for the activities of non-intervention studies/investigator initiated trials.
- Coordinate the review and approval of medical materials and locally developed promotional materials; ensure that the medical materials provided from the world or the region for participation and stakeholder events are adapted to local needs and reviewed/approved according to local/P3 guidelines.
- Ensure that medical knowledge is provided for cross-functional groups, including: Pharmacovigilance, regulatory affairs, market access, quality control, commercial teams, brand team and others.
- Responsible for the identification and evaluation of risks, mitigation planning, and the implementation and monitoring of appropriate internal controls within the area of responsibilities. Notification of technical complaints/adverse events/special case scenarios related to Novartis products within 24 hours of receipt.
- Notification of technical complaints/adverse events/special case scenarios related to Novartis products within 24 hours of receipt.
- Marketing sample distribution (where appropriate).
Essential Requirements
- Bachelor's Degree / Desirable Scientific background.
- Working experiences in Medical Affairs.
- At least 4 years of experience in the pharma industry.
- Deep understanding of the field roles.
- Experience in data generation.
Languages:
- Local language: fluent written and spoken
- English: fluent written and spoken
Benefits and Rewards:
Company Pension Plan, Life and Accidental Insurance, Meals Allowance or Canteen in the office, Flexible working hours. Read our handbook to learn about all the ways we'll help you thrive personally and professionally: Novartis Life Handbook
Commitment to Diversity and Inclusion / EEO
Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve
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
Division
International
Business Unit
Innovative Medicines
Location
Spain
Site
Madrid Provincial
Company / Legal Entity
ES06 (FCRS = ES006) Novartis Farmacéutica, S.A.
Alternative Location 1
Barcelona Provincial, Spain
Functional Area
Research & Development
Job Type
Full time
Employment Type
Regular
Shift Work
No
