Main Missions 

Under the responsabilities of Neurotrials’ director, your missions will be:

• To Manage NEUROTRIALS Medical part
• To Provide contribution / Input to the medical documentation
• Medical monitor for clinical trials conducted at the ICM in partnership with the pharma/biotech/medtech companies
• To provide medical expertise in protocol design
• To Participate in protocol reviews and provide scientific and clinical expertise
• To provide medical expertise for the baseline of the study
• To provide medical review of clinical data
• To review eligibility criteria
• To be the main contact for the patients’ safety in the study
• To contribute, review and write some SOPs
• To provide the medical training of the project team necessary for the proper conduct of clinical studies
• To be the link between the sponsor and the investigator site and the KOLs 

Know-How

• You have a past experience in medical monitoring of 1 year minimum within CRO, pharmaceutical or biotech companies or clinical research structure

Background

• Degree in medecine
• Degree in Neurology is a plus
• PhD is a plus
• Skills in Clinical trials Methodology is a plus
• Fluent in English
• Knowledge of GCP-ICH
• Good listening and communication skills
• Diplomacy and adaptability

Face-to-face is essential. Possibility of one day of teleworking