Experienced CRA for Global Trials — Belgium

IQVIA LLC

Zaventem

Sur place

EUR 52 000 - 76 000

Plein temps

14 jours+
Générateur de candidature

Une candidature complète en une minute — un CV et une lettre de motivation personnalisés, prêts à être envoyés.

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Avantages offerts par ce poste

Company car
Mobile phone
Attractive benefits package

Résumé du poste

A leading global clinical research provider is seeking a Clinical Research Associate in Zaventem, Belgium. This full-time position involves performing site management tasks, developing recruitment plans, and ensuring compliance with regulatory standards. Candidates should have a university degree in a scientific discipline, experience in the pharmaceutical industry or clinical trials, and proficiency in Dutch, French, and English. A supportive work environment and career growth opportunities are provided.

Qualifications

  • Experience in Pharma Industry or Clinical Trials environment.
  • Excellent command of Dutch, French, and English language.
  • Flexibility to travel is required.

Responsabilités

  • Perform site selection, initiation, monitoring, and close-out visits.
  • Support the development of a subject recruitment plan.
  • Evaluate the quality and integrity of site practices.
  • Manage progress by tracking regulatory submissions.

Connaissances

University degree in scientific discipline or health care
Experience in Pharma Industry or Clinical Trials
Excellent command of Dutch, French, and English
Very good computer skills including MS Office
Organizational skills
Time management skills
Problem-solving skills
Flexibility to travel
Ability to establish and maintain effective relationships

Formation

University degree in scientific discipline or health care

Outils

MS Office

Description du poste

A leading global clinical research provider is seeking a Clinical Research Associate in Zaventem, Belgium. This full-time position involves performing site management tasks, developing recruitment plans, and ensuring compliance with regulatory standards. Candidates should have a university degree in a scientific discipline, experience in the pharmaceutical industry or clinical trials, and proficiency in Dutch, French, and English. A supportive work environment and career growth opportunities are provided.
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