CRA en Morgan Philips Hudson Executive Search

Morgan Philips Hudson Executive Search | (3) ofertas activas
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Nuestra inversión en tecnología digital, aproximación científica a la evaluación del candidato y acceso a nuestra selecta red de expertos global nos hacen destacar en el mercado español.

Nos desmarcamos de las técnicas tradicionales de los headhunters, con un enfoque completamente transparente y basado en datos. Garantizamos a nuestros clientes que los candidatos incorporados encajan con su organización.
Madrid, 17 Oct.
At AstraZeneca, we're not afraid to do things differently. We're building a new kind of organization to reset expectations of what a bio-pharmaceutical company can be. This means we're opening up new ways to work, pioneering cutting edge methods and bringing unexpected teams together.

We lead our industry in our development of a strong and varied pipeline. This means our people are here to win, we give you a breadth of opportunities to be curious and do cutting edge, unique work that has big impact on science and medicine.

As Clinical Research Associate (CRA) you will be responsible for the delivery of the studies at allocated investigator sites and will active participate in the local study team(s). You will work in close collaboration with other CRAs and the Local Study Team to ensure that quality and quantity commitments are achieved in a timely and efficient manner.

The CRA is responsible for the preparation, initiation, monitoring and closure of assigned sites in clinical studies, in compliance with AZ Procedural Documents, international guidelines such as ICH-GCP, and relevant local regulations and that the sites deliver according to their respective commitment in the individual studies.

Numero de vacantes: 1
Bachelors degree in related discipline, preferably in life science.
Experience as CRA from either a pharmaceutical company or a CRO of more tan 2,5 years is required.
Location Madrid.
Excellent knowledge of international guidelines ICH-GCP, basic knowledge of GMP/GDP.
Fluent knowledge of spoken and written English: B2.2.
Good knowledge of relevant local regulations.
Good medical knowledge and ability to learn relevant AZ Therapeutic Areas .
Basic understanding of the drug development process.
Good understanding of Clinical Study Management including monitoring, study drug handling and data management.

Excellent attention to details.
Good written and verbal communication skills.

Good collaboration and interpersonal skills.

Good negotiation skills.

Ability to travel nationally/internationally as required.

Estudios mínimos
Experiencia mínima
2 años
Disponibilidad para viajar
El 20% del tiempo laboral

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