Clinical Site Services
Our three, fully equipped research clinics in the Tampa Bay area provide easy access to over 3 million potential patients in the tri-county area of Hillsborough, Pinellas and Pasco counties. Our clinics are equipped with medical exam rooms, private consultation areas, full vital sign, phlebotomy and EKG capabilities, centrifuges, minus 20 freezers, secure ambient and refrigerated medication storage, high speed internet, dedicated monitoring spaces as well as secure, climate controlled document storage.
We have an excellent reputation with past and present clients in consistently meeting and most often exceeding recruitment goals (often ahead of schedule), providing efficient and accurate data entry (case report forms and most current EDC platforms) and completing quick query resolution. We process all regulatory documents and execute clinical trial agreements typically within 5-7 days. Please contact us if you are interested in viewing our Clinical Trial Portfolio that contains information on the clinical trials we have completed as well as metrics supporting enrollment and retention data. email@example.com
We offer single-site clinical trial management services and are experienced in protocol development and design, study timeline development, assessment and analysis of study management costs, recruitment strategies, IRB submissions, as well as suggesting resources for data management and statistical analysis.
Clinical Trial Recruitment
Situated in a large ethnically and chronologically varied population of the Tampa Bay area, we have access to a very large and diverse pool of potential patients. We have a robust recruitment database using Real:Time CTMS, clinical trial management system (21 CFR Part II compliant) with over 4,000 past and present subject data. We have an excellent team of experienced, highly motivated, bilingual (English/Spanish) recruiters that facilitate rapid enrollment.
Clinical Staff Qualifications
Our highly experienced team of investigators and coordinators are well trained in clinical trial management, protocol adherence and patient safety. We promote certifications from SoCRA and ACRP as well as require GCP training every 2 years using industry leaders such as: SoCRA, ACRP, CITI (Collaborative Institutional Training Initiative), Barnett International and IMARC Research, Inc.
Our investigative team consists of board certified physicians who have collectively conducted research for more than 30 years, as well as a group of highly experienced Nurse Practitioners.
Our highly skilled clinical research coordinators are a collection of RN’s, certified medical assistants, as well as industry veterans, many with more than 10 years of experience. They are competent in all stages of clinical trial management and have experience in completing all phases of research in numerous clinical indications. Our coordinators maintain IATA and CPR certification, many are validated acne raters and maintain competency in phlebotomy and performing EKGs. We also have staff that are certified adhesion evaluators and patch graders.