Medical Monitor
Il y a 4 mois
Prise de poste : 01/10/2024 BAC +3/+4 Paris
Nombre de poste : 1 CDI De 40k à 50k euros
**Description du poste et des missions**:
**Position to be filled as soon as possible | Permanent position**
- The Paris Brain Institute is a private foundation recognized as being of public interest, dedicated to fundamental and clinical research on the nervous system. On a single site, 800 researchers, engineers and doctors cover the full range of neurological disciplines, with the aim of accelerating discoveries about how the brain works, and the development of treatments for diseases such as Alzheimer's, Parkinson's, multiple sclerosis, epilepsy, depression, paraplegia, tetraplegia and others. The Neurotrials unit is an early-stage clinical research unit within the ICM for the design, management and execution of phase Ib/IIa clinical trials in drug development or in the field of medical devices._
**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
**Profil souhaité**:
**_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
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