- Review of presentations (could edit this to suit a previous piece of work)- Double blind
trials - RAG the specification (included)- Essay title, structure for
planning and detailed mark scheme and feedback
form included on presentation.
Prepare Coordinate, review and finalization of various clinical operations /
trial - related documents (i.e., Trial master file, protocols / amendments, informed consent forms, Study operations manuals / sheets, advertisements, data management / analysis plans and clinical study reports) according to ICH - GCP guidelines and CFR Part 11 for completeness, accuracy and legibi
trial - related documents (i.e.,
Trial master file, protocols / amendments, informed consent forms, Study operations manuals / sheets, advertisements, data management / analysis plans and clinical study reports) according to ICH - GCP guidelines and CFR Part 11 for completeness, accuracy and legibi
Trial master file, protocols / amendments, informed consent
forms, Study operations manuals / sheets, advertisements, data management / analysis
plans and clinical study reports) according to ICH - GCP guidelines and CFR Part 11 for completeness, accuracy and legibility.