Each of the centers has multiple experienced investigators and a full-time Premier Research staff that is highly trained and experienced. Our most recent FDA audit in September 2009 resulted in no substantial findings and no FDA 483 was issued. Our group of clinical research coordinators is comprised of over 50% licensed staff including registered nurses, licensed practical nurses, and emergency paramedics. Our clinical research coordinators have an average of four years experience in clinical trials. Our sites offer state-of-the-art recruiting and research facilities plus the ability to handle the most scientifically demanding trials in a range of therapeutic areas. Our services include:
- Protocol Review
- Rapid Feasibility Assessments
- Informed Consent Form Development
- Source Document Development
- Rapid IRB Submission
- Rapid Subject Recruitment utilizing extensive subject databases
- Specimen Collection and Processing
- Data Collection using both paper CRF and eCRF
- Collection of Patient Reported Outcomes (PROs) using electronic and paper diaries
- Project Management