Netherlands Job Openings
QPS
Clinical Research Associate (CRA)
Groningen
FULL TIME
August 1, 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 with prior clinical trials monitoring experience for the position of Clinical Research Associate in the near future. Note that this role may also be filled in Austria (QPS Clinical Services Gmb H is in Graz, Austria).
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 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.
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 CRO field is a plus; our ideal candidate will have solid prior CRA work experience (specifically, extensive experience monitoring clinical trials). 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. You will be able to travel to your assigned clinical trial sites (may occasionally include overnight travel).
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. You will also have the opportunity to work from your home office in the Netherlands or Austria!
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
Vaccination protocol
As an employee of QPS you are expected to participate in the vaccination program of QPS for Health purposes. This vaccination program includes a Hepatitus B vaccination. By applying for this job, you automatically accept to participate in this vaccination program when hired. For details you can ask the HR department.
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 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.
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 CRO field is a plus; our ideal candidate will have solid prior CRA work experience (specifically, extensive experience monitoring clinical trials). 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. You will be able to travel to your assigned clinical trial sites (may occasionally include overnight travel).
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. You will also have the opportunity to work from your home office in the Netherlands or Austria!
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
Vaccination protocol
As an employee of QPS you are expected to participate in the vaccination program of QPS for Health purposes. This vaccination program includes a Hepatitus B vaccination. By applying for this job, you automatically accept to participate in this vaccination program when hired. For details you can ask the HR department.
New Job Alerts
Thermo Fisher Scientific
Installation Engineer II, Field Service
FULL TIME
November 9, 2024
View Job DescriptionCérélia Netherlands B.V.
Supply Chain Specialist
Sliedrecht
FULL TIME
November 9, 2024
View Job DescriptionLooking for similar job?
Thermo Fisher Scientific
Clinical Trial Coordinator - Netherlands
Ede
FULL TIME
August 2, 2024
View Job DescriptionQPS, LLC
Clinical Trial Assistant (based in Europe)
Groningen
FULL TIME
July 30, 2024
View Job DescriptionBoston Scientific Corporation
Electrophysiology Field Clinical Specialist (Netherlands)
Utrecht
August 2, 2024
View Job DescriptionNew Job Alerts
Thermo Fisher Scientific
Installation Engineer II, Field Service
FULL TIME
November 9, 2024
View Job DescriptionCérélia Netherlands B.V.
Supply Chain Specialist
Sliedrecht
FULL TIME
November 9, 2024
View Job Description