1 Site & PI identification as per the specific needs of Client & Protocol 2 Regulatory submission 3 IRB submission 4 Site set up 5 Document collection 6 Create source document template 7 Prepare site for SIV 8 Pre screening, in case of chronic disease trials 9 Enroll & Follow Up 10 Assist in the ICF process, screening & enrollment 11 Coordinate subject follow up visits - prevent lost to follow up & missed visits 12 Manage CTM accountability, distribution & logistics 13 Coordinate Central Lab logistics & sample flow 14 Coordinate Monitoring & Audit visits 15 Subject reimbursements 16 Safety - Coordinate SAE reporting on time 17 TMF - Maintain and update the file 18 Post trial Activities 19 Training - Project Specific & ICH GCP 20 Investigator Meet - Organize multicentric trial meetings 21 Contracts - Coordinate with all parties 22 Financials - Coordinate for all milestone payments 23 Create and Maintain local PI / Facility database.