Senior Clinical Research Associate
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- Manage clinical study activities for assigned study sites across one or more clinical projects
- Conduct site monitoring visits and maintain regular communication with site personnel
- Ensure patient safety and wellbeing are maintained throughout the study
- Support the operational execution of clinical trials and ensure collection of high-quality data
- Verify Investigator Site Files are maintained according to regulatory and company requirements
- Support patient recruitment and retention activities
- Identify, escalate, and assist in resolving site-related issues
- Ensure compliance with study protocols, regulatory requirements, and company procedures
- Collaborate with investigators, ethics committees, vendors, and internal stakeholders
- Serve as a reliable source of study site status and progress updates
- Support implementation of new clinical systems and processes Requirements
- Bachelor's degree in Life Sciences, Biological Sciences, Nursing, Physical Sciences, or a related field
- Minimum 4 years of recent site monitoring experience as a CRA
- Previous clinical research experience
- Medical device or MedTech monitoring experience
- Strong knowledge of GCP and clinical research regulations
- Relevant certifications such as CCRA, RAC, or CDE are desirable
- Strong communication, presentation, and organizational skills
- Ability to manage multiple priorities and deadlines
- Willingness to travel up to 80%
- Fluency in English and Dutch is required Contract Type
- Freelance / Contract
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