Roseval C.

Administrative: English | Copywriting | Technical Writing | Email Marketing | Content Writing | Meeting Minutes As a Clinical Research Professional (Current), Technical skills: Regulatory Start-Up | Regulatory and Ethics Committee Submission Dossier | Clinical Research Protocol Development | Data Review and Monitoring | Source Document Review and Verification (including patient records) | Data Analysis | GCP | CTMS | Medidata | Veeva As an Industrial Pharmacist (Previous), Technical Skills: cGMP | Quality assurance | Pharma containment | Validation | Protocol writing | Report generation | User manual writing | Process Improvements | Technology Transfer