197 days ago on michaelpage.ch

Clinical Trainer (m/w)

Michael Page International (Suisse) SA

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 Please refer to JobSuchmaschine in your application

Clinical Trainer (m/w)

*Train Gynecologists and Embryologists to the use of company's procedure *Train Nurses and Clinical Research Assistants for the clinical procedure and SOPs *Maintain records and reports of training activities *Maintain capture of clinical data *Maintain an open dialogue with the clinic personnel to identify improvements in the procedure *Assist the CSO and Lead Clinical Trainer in the development of workflows and action plans to facilitate the overall optimization of the training. *Report back to the CSO

Clinical Trainer

Implantable Medical Devices

*Bachelor's degree is required, Master's degree in biology or equivalent is preferred *Minimum of three (3) years related experience in delivering training to clinical staff with a delivery performance track record *Experience in lab procedures and the use of medical devices *Experience in medically assisted reproduction would be a plus *High level of independence and initiative *Execution and Detail oriented *Team player with authority and excellent inter-personal and communication skills *Fluency in English, additional languages like French and Spanish would be a plus *Willing to travel more than 50%

Our client is a life sciences company focused on the development and commercialization of novel technologies in the field of medically assisted procreation with the aim of improving results and the overall quality of care through the use of more physiologic and natural processes. The company is progressively starting the commercialization of his medical device for the Natural Fertilization procedure within a selected group of leading clinics in Europe.

*A unique opportunity to join a successful, growing company that is at the core of a major innovation in assisted reproductive medicine and is now in the process of bringing its first procedure to the market. *As part of a small team, the possibility to work also on a variety of interesting activities like participating in clinical trials, maintaining the Quality and Regulatory system documents