- Protocol development
- Coordination of feasibility survey to sites
- Assistance with funding applications
- CRF development
- Development of trial-related documents and resources (Trial Master File)
- Development of Standard Operating Procedures (SOPs)
- Centralised and site ethics applications (NEAF, NAF)
- Assistance with site governance applications (CTN, Medsafe)
- Labelling/distribution of medication
- Trial budget projections