MAIN MISSIONS

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

- To Manage NEUROTRIALS’s 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.

Apply on our career site with your resume and cover letter in English in a single document : https://offres.institutducerveau-icm.org//fr/jobs/1813-81 />