clinical research associate jotec

Voor een geneesmiddelenonderzoek gericht op een nieuw middel tegen cholestatische leverziekten zoeken wij deelnemers die bereid zijn tijdelijk in een onderzoekscentrum te verblijven. Het onderzoek bestaat uit een primaire verblijfsperiode in het centrum, begeleid door artsen en verpleegkundigen die dagelijks gezondheid en veiligheid monitoren. Tijdens de...

Overview In this role you will support a single sponsor as a Clinical Research Associate within IQVIA's FSP model. You'll manage and monitor sites across the country, contribute to patient recruitment plans, and ensure protocol training and compliant study execution. You will work in a collaborative setup with a dedicated line manager and benefit from...

pJoin our global team dedicated to innovation and initiative, where physical walls and different time zones don’t limit, but encourage, collaboration. Where all contributions and new ideas are explored with an open mind and work is driven by our shared values: be courageous, be accountable, be honest, be inclusive and elevate others. /ph3Job Description...

Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to put patients first — developing innovative medical technologies that improve the lives of 72+ million patients each year. Your unique...

Overview In this role you will work as a dedicated CRA within IQVIA's sponsor-aligned clinical FSP setup. You'll manage sites and monitor study progress across the country, focusing on patient recruitment and protocol training. You will produce monitoring reports, drive action plans, and support junior team members as needed. Your work helps advance...

Overview As a Clinical Research Associate II at Precision for Medicine, you will oversee site performance to ensure studies are conducted per protocol and regulatory standards. You'll work remotely in the Netherlands with site visits to monitor progress and support study setup. You'll collaborate with cross-functional teams to mitigate risks and maintain...

Overview In this role you enable medicinal innovations by conducting rigorous on-site monitoring and site management for clinical studies. You'll work within our Functional Services Provider team to ensure protocols and regulatory requirements are met, while collaborating with cross-functional partners. The position focuses on data integrity, regulatory...

Are you seeking an exciting and fulfilling new opportunity? Join our dynamic team at WEP Clinical, where your contributions will play a key role in driving impactful solutions and improving outcomes for clients and patients. We encourage innovation and collaboration, challenging our team to bring forward ideas that make a real difference. Be part of a...

Overview In this role you will support a single sponsor as a Clinical Research Associate within IQVIA's FSP model. You'll manage and monitor sites across the country, contribute to patient recruitment plans, and ensure protocol training and compliant study execution. You will work in a collaborative setup with a dedicated line manager and benefit from...

Overview As a Clinical Research Associate II in the Netherlands, you monitor clinical studies at investigative sites to ensure compliance with protocols, SOPs, and ICH-GCP. You will support study setup, regulatory activities, and site visits, while using your expertise to manage risks and drive quality outcomes. The role offers remote work with...

Overview As a Clinical Research Associate II at Precision for Medicine, you will oversee site performance to ensure studies are conducted per protocol and regulatory standards. You'll work remotely in the Netherlands with site visits to monitor progress and support study setup. You'll collaborate with cross-functional teams to mitigate risks and maintain...

Overview In this role you will work as a dedicated CRA within IQVIA's sponsor-aligned clinical FSP setup. You'll manage sites and monitor study progress across the country, focusing on patient recruitment and protocol training. You will produce monitoring reports, drive action plans, and support junior team members as needed. Your work helps advance...

Overview In this role you will support a single sponsor as a Clinical Research Associate within IQVIA's FSP model. You'll manage and monitor sites across the country, contribute to patient recruitment plans, and ensure protocol training and compliant study execution. You will work in a collaborative setup with a dedicated line manager and benefit from...

Overview As a Clinical Research Associate II at Precision for Medicine, you will oversee site performance to ensure studies are conducted per protocol and regulatory standards. You'll work remotely in the Netherlands with site visits to monitor progress and support study setup. You'll collaborate with cross-functional teams to mitigate risks and maintain...

Overview As a Clinical Research Associate II in the Netherlands, you monitor clinical studies at investigative sites to ensure compliance with protocols, SOPs, and ICH-GCP. You will support study setup, regulatory activities, and site visits, while using your expertise to manage risks and drive quality outcomes. The role offers remote work with meaningful...

Overview In this role you enable medicinal innovations by conducting rigorous on-site monitoring and site management for clinical studies. You'll work within our Functional Services Provider team to ensure protocols and regulatory requirements are met, while collaborating with cross-functional partners. The position focuses on data integrity, regulatory...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Us as a Clinical Research Associate in our client dedicated FSP team - Netherlands. Make an Impact at the Forefront of InnovationWe have successfully supported the top 50 pharmaceutical companies and more than 750 biotech, spanning 2,700 clinical trials across 100+ countries in...

Overview In this role you will support a single sponsor as a Clinical Research Associate within IQVIA's FSP model. You'll manage and monitor sites across the country, contribute to patient recruitment plans, and ensure protocol training and compliant study execution. You will work in a collaborative setup with a dedicated line manager and benefit from...

pOur client is seeking a dedicated and experienced Pharmaceutical Clinical Research Associate (CRA) to support their ongoing clinical trials, primarily focusing on the Randburg area. This vital role involves monitoring clinical trial sites to ensure compliance with protocols, regulatory requirements, and data integrity. You will act as the key liaison...

pOur client is seeking a dedicated and experienced Pharmaceutical Clinical Research Associate (CRA) to support their ongoing clinical trials, primarily focusing on the Randburg area. This vital role involves monitoring clinical trial sites to ensure compliance with protocols, regulatory requirements, and data integrity. You will act as the key liaison...