Outsourcing

•  Clients can outsource any task in clinical research to CR Clinical to execute.  

Study Start Up

•  Feasibility
• IRB Submissions
• Informed Consent Review
• Site Agreements
• Protocol Review
• Site Selection
• Site Training

On-site/Remote Monitoring

• Qualification Visits
• Site Initiation Visits
• Monitoring Visits
• Termination Visits

Site Management

• Electronic Data Capture Training
• Study Specific Training
• IRB Submission
• Regulatory Review
• Quality Assurance

Staffing

 

• CR Clinical can provide all staff needed for a clinical trial and oversee the trial in its entirety (from start-up to completion). 
• CR Clinical has a database of experienced contract CRAs who are available for work along with a database of entry level and experience clinical research personnel.
• CR Clinical will help recruit experienced staff such as clinical research associates, clinical study coordinators, project managers, data managers, statistician, clinical enrollment specialist, and any clinical staff needed.
• CR Clinical can help recruit permanent, temp, temp to hire, and contract staff personnel globally.