Clinical Research Associate Madrid

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Clinical Research Associate Madrid

  • Ref: 1869265
  • COVANCE

  • Madrid
  • Inscripción cerrada
  • 30 inscritos
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Jornada sin especificar - Contrato sin especificar - Retribución sin especificar - Hasta 15 años de experiencia

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Comparte:

Empresa

Covance Laboratories

Covance is one of the world's most exciting and professional drug development services companies (CRO), providing integrated, tailored solutions to the pharmaceutical and biotechnological industries.

You can make a difference by helping to deliver life-saving and life-enhancing medicines to people around the world.

Covan has several CRA opportunities for you in various regions of Spain : this is a great moment to join us!
  • UK
  • Farmacia y Material Hospitalario
  • COVANCE
Descripción de la oferta

Descripción de la oferta

Duración de la oferta: hasta el 15/10/2015

Funciones

Our Clinical divisions currently have several needs for Clinical Research Associates:

* Outsourcing division:
- jr CRA or CRA trainee - client-based - Barcelona.
- CRAs (3 to 4 yrs Experience including oncology) - home-based - Madrid
and Barcelona.

* Internal Clinical Operations division:
- CRA (min 1 yr monitoring Experience ) - office-based - Madrid.

Requisitos

- Education/Qualifications - University/college degree (life science preferred), or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing certification, medical or laboratory technology).
- Thorough knowledge of ICH Guidelines and GCP including a basic understanding of regulatory requirements.
- Thorough knowledge of monitoring procedures.
- Basic understanding of the clinical trial process.
- Experience - Minimum 2 yrs up to 5 years of monitoring Experience (including pre-study, initiation, routine monitoring and closeout visits) - oncology Experience highly preferred.
- Ability to monitor study sites independently according to protocol monitoring guidelines, SOPs, GCP and ICH Guidelines.
- Oncology Experience is a definite plus
- Experience with phase I would be appreciated for the ECD division.
- Have a full understanding of the Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs.
- Good planning, organization and problem solving abilities.
- Ability to work with minimal supervision.
- Good communication and interpersonal skills.
- Good analytical and negotiation skills.
- Computer competency.
- Fluent in English and local language, both written and verbal.
- Works efficiently and effectively in a matrix environment.

Se ofrece

- The opportunity to pursue further training and an interesting career in an inspiring environment that values achievement, supports a balance between your personal and professional life and allows you to make meaningful contributions.
- Flexible conditions and an attractive remuneration package.
  • Área

    Sanidad, salud y servicios sociales

  • Categoría o nivel

    Mandos

  • Nº Vacantes

    1

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