R&d manager

Pharmaceutical Company.
Reporting to the General Manager and working under the supervision of the Group VP Development, the R&D Manager manages R&D projects within a time frame and a given budget. He provides strong input in the group regulatory strategy and expertise on all aspects of clinical operations.

The R&D Manager conducts the pharmaceutical and clinical development of projects under his/her responsibility, in close collaboration with R&D dedicated team members and/or Affiliates employees involved in R&D. He provides guidance and support to the group regulatory strategy. He will design and construct the clinical development plan in compliance with regulatory guidelines and requirements. He is in charge of the design, the development and the implementation of the clinical studies and contributes to the building of the submission dossier.

Management of R&D projects in close collaboration with R&D team:

- In collaboration with the Pharmaceutical Development Manager, contribute to the develop

Imprescindible:

• Residir en Madrid
• Graduado Escolar
• 1 Año de experiencia

Se ofrece:

Salario: A negociar
Contrato: Indefinido
Duración: Indefinido
Jornada: Completa

Se requiere:

Degree in Medicine or Life Science. Postgraduate or Master of Science in Clinical Research and Regulatory Administration will be considered a plus.

Experience:
- The candidate will have a minimum of 7 years of experience in clinical research and regulatory affairs in pharmaceutical industry.
- Strong knowledge of regulations, guidelines and European registration processes.
- Experience in pharmacology, medical device, food complement desirable to provide input to the disease area strategy.
- Strong knowledge of Good Clinical Practices and international clinical regulatory requirements.
- Knowledge of the drug development process.

Excellent English and Spanish skills, both oral and written, are required.
French will be considered a Plus.

Se desea:

Degree in Medicine or Life Science. Postgraduate or Master of Science in Clinical Research and Regulatory Administration will be considered a plus.

Experience:
- The candidate will have a minimum of 7 years of experience in clinical research and regulatory affairs in pharmaceutical industry.
- Strong knowledge of regulations, guidelines and European registration processes.
- Experience in pharmacology, medical device, food complement desirable to provide input to the disease area strategy.
- Strong knowledge of Good Clinical Practices and international clinical regulatory requirements.
- Knowledge of the drug development process.

Excellent English and Spanish skills, both oral and written, are required.
French will be considered a Plus.