Bordeaux, Nouvelle-Aquitaine, France
Best in-class partner for FSP, Resourcing and Full Service clinical trial project management from Phase I (no HV)-IV: ◻️Medical Writing - Protocol development - Protocol Feasibility ◻️Site Feasibility (Site Identification, recruitment) ◻️Regulatory submission ◻️Site contracts ◻️Site Monitoring & Management ◻️Project Management Activities ◻️Drug safety and pharmacovigilance ◻️Medical Monitoring ◻️Data Management ◻️Statistics ◻️eTMF (Trial Master File) ◻️Medical Writing - Clinical Study Report (CSR)
✔️ Important volonteer base for clinical trials