Netherlands Job Openings
QPS, LLC
Clinical Research Associate - NL
Groningen
FULL TIME
July 30, 2024
QPS Netherlands B.V. in Groningen is part of an international organization and conducts drug research on behalf of international pharmaceutical and biotechnological companies. To strengthen our Clinical Research department in Groningen, we are looking for candidates for the position of Clinical Research Associate in the near future.
What will you do?
In this role, you will monitor clinical drug studies across various research centers according to applicable guidelines such as GCP and WMO. You will manage studies from site initiation to close-out, communicate with clients, conduct regular site visits, and write reports. You will verify data, check study drug accountability, discuss study progress and issues with site staff, and review various aspects of execution, processes, samples, and materials. Monitoring activities will primarily take place at our clinics in Groningen and Leeuwarden. You will work as part of a team but also independently during visits to research centers. The hours are flexible, and you will work from home.
Work Location
Who are you?
Ideally, you have a bachelor's degree, or an academic level obtained through education and/or experience with a (para)medical or biological background. A few years of experience in the field is a plus. You are expected to work precisely and organized, and to communicate effectively. You are proactive with an eye for detail. You have a good command of both Dutch and English, spoken and written.
What do we offer?
We offer a varied role within a dynamic and international organization. We provide a full-time position of 32-40 hours per week for at least one year. After one year, there may be an opportunity for extension.
Want to know more?
Want to know more? Visit our website to learn more about QPS; www.qps.com. Are you ready to apply? We would like to receive your motivation and CV (in English). If you have any questions, please contact our Human Resources team at HRM.NL@qps.com
What will you do?
In this role, you will monitor clinical drug studies across various research centers according to applicable guidelines such as GCP and WMO. You will manage studies from site initiation to close-out, communicate with clients, conduct regular site visits, and write reports. You will verify data, check study drug accountability, discuss study progress and issues with site staff, and review various aspects of execution, processes, samples, and materials. Monitoring activities will primarily take place at our clinics in Groningen and Leeuwarden. You will work as part of a team but also independently during visits to research centers. The hours are flexible, and you will work from home.
Work Location
Netherlands, Groningen; ask about our flexible work options.
Who are you?
Ideally, you have a bachelor's degree, or an academic level obtained through education and/or experience with a (para)medical or biological background. A few years of experience in the field is a plus. You are expected to work precisely and organized, and to communicate effectively. You are proactive with an eye for detail. You have a good command of both Dutch and English, spoken and written.
What do we offer?
We offer a varied role within a dynamic and international organization. We provide a full-time position of 32-40 hours per week for at least one year. After one year, there may be an opportunity for extension.
Want to know more?
Want to know more? Visit our website to learn more about QPS; www.qps.com. Are you ready to apply? We would like to receive your motivation and CV (in English). If you have any questions, please contact our Human Resources team at HRM.NL@qps.com
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