Ofertas de empleo
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AVISO: Esta oferta no se encuentra activa.
Oferta de Trabajo |
Código: 41375
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Puesto: Clinical project manager |
Función: Designing, planning, and supervising the implementation of the clinical trials for our products, according to applicable regulations.Determining effective strategies for promoting/recruiting research participants and retaining participants. |
Empresa: CORIFY Care
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Nº de Plazas: 1 |
Referencia: 20211004_CPM |
Publicada el 4/10/2021 |
Publicada hasta el 25/10/2021 |
Tipo de Contrato: Indefinido |
Dedicación: Jornada completa |
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Localidad: Sin determinar |
Provincia: -- |
Disponibilidad para viajar: Si, Internacional |
Fecha de Incorporación: Lo antes posible |
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Enlace URL:
www.corify.es
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Titulación Académica |
Biología (Titulación Universitaria)
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Bioquímica (Titulación Universitaria)
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Ciencias Biomédicas (Titulación Universitaria)
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Áreas tecnológicas |
E-051 Sistemas certificados de calidad |
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Idiomas |
Idioma: Inglés |
Nivel Lectura: Alto |
Nivel Escrito: Alto |
Nivel Conversación: Alto |
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Conocimientos de Informática |
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Experience in clinical evaluations according to both EU and US regulations. |
Experiencia |
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3 years of experience in clinical trial and clinical evaluation for medical devices. Bachelor degree in Life Sciences -related or scientific discipline. Proficient knowledge of regulations related with clinical evaluation (e.g., ISO 14155). |
Otros |
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Corify Care is a start-up focused on introducing a novel medical device to map cardiac arrhythmias in real time non-invasively. This novel technology will improve the treatment in more than 10 million atrial fibrillation patients only in Europe. Our non-invasive electro-anatomical mapping system displays the activation patterns in each point of the heart without the need for invasive catheters, allowing the possibility to map all arrhythmia patients even during a regular visit to the cardiologist.
As a Clinical Project Manager at Corify, your main functionalities will be:
- Designing, planning, and supervising the implementation of the clinical trials for our products, according to applicable regulations.
- Determining effective strategies for promoting/recruiting research participants and retaining participants in long-term clinical trials.
- Developing consent forms and other required documentation for their approval by Ethics Committees.
- Coordinating new protocol submissions, renewals, revisions and reports to applicable regulatory agencies.
- Coordinating CER drafting.
- Supervising the implementation of and adherence to study protocol, and providing support in analyzing the data. Ensuring that the study protocols are conducted in compliance with applicable regulations.
- Keeping updated the technical files of our devices regarding their clinical evaluations.
- Training clinical research team members and evaluating their performance.
- Reporting to CEO.
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