Clinical Research Associate Madrid

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Clinical Research Associate Madrid

  • Ref: 1869265

  • 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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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
Descripción de la oferta

Descripción de la oferta

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


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.


- 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


  • Nº Vacantes


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