Clinical Research Associate en NOVO NORDISK PHARMA

Clinical Research Associate
NOVO NORDISK PHARMA | (2) ofertas activas
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Madrid, 15 Sep.
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Descripción
Main purpose

Reporting to Clinical Research Manager you will be responsible for overseeing the progress of a clinical trial, typically on-site, and ensuring that the trial is conducted, recorded and reported in accordance with the protocol, study guidelines, SOPs, and applicable regulations.

Key Accountabilities

- Conducting trial/site management in accordance with protocol, SOPs, LOPs, ICH-GCP guidelines and local legislation, including sites selections, obtaining necessary approvals and documentation, site initiations, monitoring and SDV, management of site recruitment performance, trial supplies management, handling of safety information, data cleaning activities, close-out and archiving.

- Achieving close liaison with Project Management, Data Management and HQ throughout the trial to ensure milestones achieved.

- Updating required IT Systems following every site visit.

- Work according to local law, Business Ethics, NNWay and NN policies & guidelines.

Numero de vacantes: 1
Tipo de contrato: Indefinido
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Requisitos
- Life Sciences Degree, ideally with a post graduate qualification in Research.

- At least 2 years’ experience in monitoring trials in accordance with ICH GCP methodology.

- Fluent English and Spanish.

Estudios mínimos
Licenciado
Idiomas
Inglés nivel Alto.
Experiencia mínima
2 años
Disponibilidad para viajar
El 20% del tiempo laboral



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