MedTech Clinical Research Associate | Travel‑Heavy

Pauwels Consulting is seeking a Clinical Research Associate to manage clinical activities across multiple study sites for medical device projects. You will monitor site performance, ensure data quality, and support regulatory compliance throughout trials.Travel up to 80% is required. Fluency in English and Dutch is essential, with experience using GCP...

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...

We are looking for an experienced Senior Clinical Research Associate (CRA) to support clinical studies within a dynamic MedTech environment. In this role, you will be responsible for managing and monitoring clinical trial activities across multiple study sites, ensuring compliance with study protocols, regulatory requirements, and quality standards.As a key...

Our client, a leading player in the MedTech industry, is seeking a Senior Clinical Research Associate to manage clinical study activities across multiple sites. This role focuses on overseeing study site performance, conducting comprehensive monitoring visits, and ensuring high-quality data collection for various medical device...

Arcadis is seeking an experienced Senior Clinical Research Associate to support and monitor clinical studies within a MedTech environment. You will manage multiple study sites, ensure protocol and GCP compliance, and drive data quality and study performance.Applicants should have 4+ years of site monitoring experience, strong communication skills, and...

We are looking for a motivated Clinical Research Associate (CRA) to support the successful execution of clinical studies within an innovative MedTech environment. In this role, you will be responsible for monitoring clinical trial activities across multiple study sites, ensuring compliance with study protocols, regulatory requirements, and Good Clinical...

We are looking for an experienced Senior Clinical Research Associate (CRA) to support clinical studies within a dynamic MedTech environment. In this role, you will be responsible for managing and monitoring clinical trial activities across multiple study sites, ensuring compliance with study protocols, regulatory requirements, and quality standards.Is this...

We are looking for an experienced Senior Clinical Research Associate (CRA) to support clinical studies within a dynamic MedTech environment. In this role, you will be responsible for managing and monitoring clinical trial activities across multiple study sites, ensuring compliance with study protocols, regulatory requirements, and quality standards.Is this...

At Gilead, we’re creating a healthier world for all people. For more than 35 years, we’ve tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer – working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight against the world’s biggest health challenges,...