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ROLE SUMMARY
For one of our clients in the Netherlands, a leading and global operating company in the area of life sciences, we are looking for skilled bioprocess technicians. Due to strong growth, we expect a total of 20-30 positions in both Up Stream Processing, Down Stream Processing and Media/Buffer Preparation.  

Seleccionamos para Compañía Farmacéutica en Madrid un/a Medical Advisor quien dará apoyo a actividades de Información Médica, Marketing así back-up Farmacovigilancia.

 

Valesta is searching for an experienced CRA 2-3 years of experience so as to join our growing team of CRAs. Office-based in Madrid, the individual will work sponsor-exclusive and will be responsible for phase I (early development) trials in onco-hematology. 

Valesta estamos buscando para importante Laboratorio Farmacéutico en Madrid un CRA I siendo deseable experiencia en Early Development (fase I) y/o onco-hematología. Se ofrece un proyecto outsourced en exclusiva trabajando en las oficinas en el centro de Madrid y con posibilidad de desarrollo. 

Se ofrece: 

Contratación estable e indefinida. 

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Clases de Inglés

Seguro Médico 

Our client, headquartered pharmaceutical company in Spain which is working at a complete international level is looking for a Clinical Quality Assurance Coordinator to ensure clinical trials (phase I-IV) compliance. 

CRA-freelance, Home Based, Germany / Italy/ France / UK and Portugal

We have a great opportunity for experienced freelances CRA who are looking to work for a private company founded by oncology experts on 12 months contract basis with possibility of extension. FTEs may range from 0.25 to 0.8.

Our client is looking for several freelances CRA with :

Valesta seleccionamos Data Managers para diversos centros hospitalarios en España (Barcelona, Madrid, Málaga..) para un proyecto de actualización y puesta al día de entrada de datos de un Ensayo Clínico en el área de Neurología.

  • Location: Madrid 
  • Office-based position
  • Permanent contract directly hired by the Company
  • Junior position 1-2 years of experience in Regulatory Affairs across different geographical territories and experience with OTC, nutraceuticals, generics and/or natural products. 
  • Travels: Not required.