APEX Research Consulting Services
APEX Research is a clinical trials consulting firm offering consulting services to small and medium sized clinical trial sites. Each member of our consulting team has over 15 years of clinical research experience. Our mission is to assist other research sites to streamline services, experience growth and increased revenues, and to help better navigate the ever-changing clinical trials landscape with our highly successful and proven methods.
APEX Research Consulting Services was started to offer our expertise to the research industry from a small site’s prospective. Our research site, Syrentis Clinical Research, is a multi-specialty research institute located in Santa Ana, CA. John Gregory Duffy, M.D. is a Principal Investigator and owner of Syrentis Clinical Research who specializes in Alzheimer’s Dementia and is a Psychiatrist with over 20 years of clinical research experience. Lorrie Bisesi, Ph.D., CCRC has over 20 years of clinical research experience and is the Vice President and Director of Clinical Operations at Syrentis Clinical Research. Our consulting team also includes a Director of Regulatory Affairs, Director of Quality Assurance/Senior CCRC, and a Director of Recruitment and Marketing. Our research center has extensive experience in geriatric, adult, adolescent and pediatric trials, and we have successfully conducted Phase two through four FDA-approved clinical trials in multiple therapeutic areas.
· Protocol Review/ IND Submission
· Vendor Setup and Management
· Study Start-Up Preparation and
Source Template Development
· IRB Submission and Oversight
· Regulatory Affairs Management
· Develop a Quality Assurance Program
· Develop effective Patient Reimbursement and Retention Programs
· Inspection Readiness Training
· New Investigator and Staff Training
· Managing PSIV and SIVs
· Preparing Feasibility Assessments
· Site Selection and Qualification Submissions
· Contract and Budget Negotiations
· Vendor Setup and Management
· Study Start-Up Preparation and Source Template Development
· IRB Submission and Oversight
· Regulatory Affairs Management
· Develop a Quality Assurance Program
· Develop effective Patient Reimbursement and Retention Programs
· Inspection Readiness Training
· New Investigator and Staff Training
· Small Research Site Business Model Review
· Streamlining a Site’s Procedures to Increase Revenue and Growth
· Increase Coordinator Productivity
· Develop Standard Operating Procedures
· Develop a strategy for Branding and Marketing
Please send us a message or call us for an appointment.
Feel free to fax any documents to (714) 542-3617
Monday - Friday: 8:00am - 5:00pm
Saturday - Sunday: Closed
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