Senior CRA: Multi-Sponsor Clinical Trials (Belgium)

IQVIA LLC; Brussel Hoofdstad; Sur place; EUR 40 000 - 60 000; Plein temps

Avantages offerts par ce poste

Company car

Mobile phone

Attractive benefits package

Flexible work schedules

Resources for career growth

Résumé du poste

IQVIA LLC is seeking an Experienced Clinical Research Associate for their Site Management team in Brussels, Belgium. This role offers the opportunity to gain experience in various therapeutic areas while managing site operations for clinical studies.

The ideal candidate will have over 2 years of experience as a CRA, possess excellent communication skills in Dutch, French, and English, and a relevant university degree. Benefits include career growth resources and flexible work schedules.

Qualifications

• Minimum 2 years of experience as a Clinical Research Associate (CRA).
• Excellent command of Dutch, French, and English.
• Driver's license class B.

Responsabilités

• Perform site monitoring visits in accordance with GCP and ICH guidelines.
• Work with sites to track subject recruitment plans.
• Evaluate the quality and integrity of study site practices.
• Manage the progress of assigned studies and regulatory submissions.
• Create and maintain documentation for site management.

Connaissances

Clinical Research Monitoring

Site Management

Communication Skills

Organizational Skills

Problem-Solving Skills

Time Management

Computer Skills (MS Office)

Formation

University degree in scientific discipline or healthcare

Description du poste

IQVIA LLC is seeking an Experienced Clinical Research Associate for their Site Management team in Brussels, Belgium. This role offers the opportunity to gain experience in various therapeutic areas while managing site operations for clinical studies.

The ideal candidate will have over 2 years of experience as a CRA, possess excellent communication skills in Dutch, French, and English, and a relevant university degree. Benefits include career growth resources and flexible work schedules.