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CLINICAL RESEARCH TO FIT YOUR NEEDS
Senior Clinical Research Independent
Ø Coordination of studies with the Project manager o Team organisation (CRAs, assistants) o Relation between biometry and data management o Collaboration with the biostatistician o Elaboration of the CRF o Creation of the planning of the study o Relation with investigational products Ø Coordination with CROs (phases I, II et III) o Choice of the CRO o Elaboration of scope of work o Follow up of the contract o Implementation of the study (administrative documents), follow up and close out Ø Co-monitoring France and Europe o Supervision of CRA and CRO o Review of reports of monitoring visits o Follow up o Respect of current regulation o Respect of planning Ø Retrieving of updated dataØ Follow up of quieries Ø Reconciliation : o of safety data o of investigational products
Services offered to conduct your studies in clinical research Ø Procedures in clinical researchØ Monitoring in clinical research Ø Training in clinical research Ø Regulatory submission of clinical trial
Freelance cra - Senior CRA - Monitoring in clinical research - Clinical trial coordination - Regulatory submission of clinical trial - Writing and implementation of procedures in clinical research - Training in clinical research - clinical research associate - clinical research indenpendent - Clinical Research Independent - Senior Clinical Research - links |
| Clinical trial coordination |
