Clinical Research Associate II/Senior Clinical Research Associate
4 weken geleden
We are seeking a Senior Clinical Research Associate to join our team in the Netherlands. As a Senior CRA, you will work independently to coordinate activities, set up and monitor studies, and ensure adherence to regulations and principles of ICH-GCP. You will also participate in preparing and reviewing study documentation, and assist in preparing regulatory submissions as requested.
Key Responsibilities:
- Coordinate activities to set up and monitor studies
- Ensure adherence to regulations and principles of ICH-GCP
- Participate in preparing and reviewing study documentation
- Assist in preparing regulatory submissions
Requirements:
- 2-3 years of monitoring experience in phase I-III trials as a CRA
- Knowledge of ICH GCP guidelines and expertise to review and evaluate medical data
- Excellent written and verbal communication in English
- Ability to produce accurate work to tight deadlines within a pressurized environment
What We Offer:
We offer a competitive salary, annual leave entitlements, health insurance, retirement planning, and a range of other benefits to support your well-being and work-life balance. We are an equal opportunity employer and are committed to providing a workplace free of discrimination and harassment. If you need a reasonable accommodation for any part of the application process, please let us know. We encourage you to apply regardless of your experience, as we are looking for the right candidate to join our team.
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