Offres d'emploi

Le poste

Imaging Technologist- Nuclear Medicine

 

Our imaging services are growing rapidly, and we are currently seeking a full-time Imaging Technologist – Nuclear Medicine to join our team in Lyon, France. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you.

Responsibilities: 

• Perform quality assurance checks on medical imaging data to ensure protocol specific requirements are met;
• Perform established image processing techniques (converting imaging formats, performing preliminary measurements of lesions and volumes) acrossNuclear medicine imaging modalities using proprietary software as well as other third party software;
• Compile and maintain project-specific status reports and trackers associated with imaging studies;
• Perform project-specific tasks in compliance with Good Clinical Practices (GCP), regulatory requirements (21CFR Part 11), applicable departmental and companywide SOPs, and project specific protocols.

Qualifications: 

• Bachelor's Degree and certification as an imaging technologist;
• Experience in Nuclear Medicine (PET/CT, SPECT/CT) needed;
• 1-3 years of experience in clinical research or imaging related field, and at least 2 years of experience as an Imaging Technologist in a hospital or imaging center;
• Experience working with clinical trials or within the pharmaceutical environment is preferred.

 

Please submit your application through the Medpace careers portal and not via email. 

 

Voir l'annonce sur le site de l'entreprise

 

 

L'entreprise

Medpace

 

Medpace is a global Clinical Research Organisation (CRO) partnering with leading pharmaceutical, biotech, and device companies to bring promising new drugs and devices to market. Medpace combines efficient clinical trial management with comprehensive regulatory consulting to provide clients with exceptional support during the drug development process. We manage the full drug and device development process for our clients which includes many components: clinical development plan preparation, project management, regulatory document preparation, safety surveillance, clinical monitoring, data management, statistical analysis, medical writing, quality assurance auditing, and regulatory submissions.

Employing almost 6,000 people across 40+ countries, our people are our biggest asset and embody our values and our approach to serving our clients. They work hard, understand our high expectations, and rise to the challenge. In return, they are rewarded with interesting projects, career advancement, and recognition. Whether you are a recent graduate or seasoned in your field, your contributions can make an impact on our business.