Site Coordination/Site Management Services

Independent site study coordination service: our educated, trained, and experienced site study coordinators (SCs) provide services at the clinical research site from the start up until the archiving period of the clinical trial.

Our study coordinator assists in:

• project planning,
• start-up activities like feasibility, selection, contracting, site team training,
• IRB related tasks,
• subject’s recruitment,
• study visits,
• monitoring visits preparation, conduct and follow-up,
• AE/SAE reporting,
• data entry, data cleaning
• lab and other result collection,
• study closure,
• IMP management,
• recordkeeping, file and document management,
• equipment and facility management, archiving.