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AVISO: Esta oferta no se encuentra activa.

Oferta de Trabajo  Código: 41375  

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 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  
Localidad: Sin determinar Provincia: -- Disponibilidad para viajar: Si, Internacional
Fecha de Incorporación: Lo antes posible  
Enlace URL: www.corify.es

Nivel Académico
Grado  

Titulación Académica
Biología (Titulación Universitaria)
Bioquímica (Titulación Universitaria)
Ciencias Biomédicas (Titulación Universitaria)

Áreas tecnológicas
A- Biociencias
E-051 Sistemas certificados de calidad

Idiomas
Idioma: Inglés Nivel Lectura: Alto Nivel Escrito: Alto Nivel Conversación: Alto

Conocimientos de Informática  
Experience in clinical evaluations according to both EU and US regulations.

Experiencia
 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

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.