We assist you in managing your study effectively within your resources and budget
- Clinical Study Support: For early stage investigators or established investigators with larger projects
- Develop study Manual Of Procedures
- Develop and maintain study regulatory binders
- Develop study specific logs and documents
- Develop and provide access to a collection of Standard Operating Procedures
- Develop study protocols
- Assist in recruitment and enrollment in clinical trials and studies
- Clinical Research Coordinator selection, interviews, and oversight
- Access to interpreters
- Work with PI to establish a monitoring plan
- Conduct study monitoring visits/checks