 |
Clinical Research (Phase II–IV)
|
 |
 |
Project management of local & international studies
|
|
|
Identification of investigational sites including feasibility & assessment of sites
|
|
|
Preparation of trial-related documents
|
|
|
Management of regulatory & ethical approvals
|
|
|
Organisation of investigators’ meetings/training of investigators
|
|
|
Set up of an administrative database to track patients & investigational sites
|
|
|
In-depth monitoring including source data verification & drug accountability
|
|
|
Management of investigators’ contracts and payments
|
|
|
Study close-out activities
|
|
|
Status reports
|
|
|
Final report
|
|
|
 |
|
