Be the clinical and technical reference for medical teams before, during and after implantations
DESCRIPTION DE POSTE
MAIN MISSIONS & ACTIVITIES
- Training of new medical centers in the context of the clinical study: Simulands, IMRR
- Patients’ eligibility evaluation within the context of clinical study using dedicated assessment software (e.g., Pie Medical 3mensio Structural Heart).
- Preparation of the Advisory panel (review of eligibility criteria of submitted cases)
- Ad-hoc support to the clinical team in product-related training and technical questions and issues.
- Case support: attending cases, crimping of the valve, Medical Training on sites with Simulands, OR setup logistics, Proctor’s engagement
- Support Clinical Sites selection ( assess OR facilities, expertise of Heart Team)
- Ensure data collection on competition (at major congresses and during sites visits, literature)
- Develop and update training material
- Responsible to update the training procedures in collaboration with QA
- Collect sites information of safety events when needed
PROFILE
1 to 3 years as a clinical product specialist in medical device field
Master’s educational background in biomedical- clinical Engineering or related field
Knowledge of ISO 13485, 5840 and DMR and other related standard regulations for class 3 medical devices
Fluent in English
Willing to travel frequently in Europe
Position based in Italy (Turin, Milano)
Master’s educational background in biomedical- clinical Engineering or related field
Knowledge of ISO 13485, 5840 and DMR and other related standard regulations for class 3 medical devices
Fluent in English
Willing to travel frequently in Europe
Position based in Italy (Turin, Milano)
CANDIDATURE
Afin de postuler à cette offre, veuillez adresser votre candidature à jobopportunities@affluentmedical.com
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