Clinical Research Associate
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Our client, a leading MedTech organization, is seeking a Clinical Research Associate to manage clinical activities across various study sites. The role focuses on overseeing site performance, conducting monitoring visits, and ensuring the delivery of high-quality data for clinical projects.
- Manage clinical study site activities and oversee performance for assigned medical device projects.
- Conduct site monitoring visits and verify the safety and well-being of study subjects.
- Execute clinical trial activities in compliance with GCP, SOPs, and applicable regulatory requirements.
- Support patient recruitment and retention activities while maintaining Investigator Site Files.
- Address and resolve site-level issues by implementing corrective and preventive actions when required.
- Interface with Investigators, IRBs/ECs, and vendors to ensure project milestones are met.
- Bachelor's degree in Life Sciences, Nursing, or a related scientific field.
- You have 2+ years of experience in clinical research, specifically involving medical device monitoring.
- You bring knowledge of international standards and regulations applied to medical devices and combination products.
- You possess proficiency in Microsoft Office and experience with clinical data systems.
- You have strong organizational skills and the ability to manage multiple sub-projects simultaneously.
- You're flexible and willing to travel up to 80% of the time to various investigator sites.
- You are fluent in English and Dutch with the ability to read medical notes and converse confidently.
Nice to Haves
- Professional certifications such as CCRA, RAC, or CDE.
- Clinical experience within the field of electro cardiophysiology.
- Active knowledge of French.
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