Information about ClinCoord
It takes a village to successfully conduct clinical trials. Our team offers specialized services to ensure that all aspects of the study are run smoothly, from regulatory compliance to data collection and analysis.
Site Support
Protocol writing support
Grant Proposal Writing Support
Completing study feasibility surveys
Assisting with trial startup, site initiation, and closeout operations
Study monitoring
Managing patient recruitment
Participant file Source Data Verification (SDV)
Managing and fulfilling staff training requirements
Post award invoicing support
Negotiating Clinical Trial Agreement and Budget
Putting together study specific site study teams
Support investigators with building study budget and budget justifications
Patient recruitment
Support site personnel hiring
Site team training and team capacity building
Assessing study patient population and present patient Epic data
Monitoring and managing study submissions and timelines
Managing Site Investigator Files and Regulatory Binders
Identifying and/or managing investigators and sub-investigators
Preparing study documents: Informed Consent Forms (ICF), legal agreements, recruitment materials, Case Report Forms (CRFs), etc.
Support data collection and timely data entry
Preparing and submitting regulatory documents
Submitting and presenting annual review reports
Maintaining study documents: training log, delegation of authority log, ICF log, pre-screening log, participant enrollment log, etc.
Get in touch to find out more