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Clinical Research Industry Speakers

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USA - Tennessee - Chattanooga
Sylvia Friedl BA CIP
Research Compliance Officer
University of Tennessee College of Medicine-- Chattanooga
Telephone: +1 (423) 778-3899.
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Experience:
Education, training and protection of human subjects in clinical trials; 20 years in academic health care
Topics:
Research ethics; clinical trial regulations; informed consent; institutional networking for protection of human subjects

USA - Tennessee - Clarksville
Kathy Maddox RN BSN CCRA
President/CEO
Alpha Clinical Research, LLC
Telephone: +1 (931) 920-2525.
Send email message
Experience:
10 years as CRC and CRA
Topics:
Working with clinical research subjects

USA - Tennessee - Jackson
Cheryl Scoledge
Director of Client Services
ProIRB Plus, Inc.
Telephone: +1 (731) 421-4622.
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Experience:
17 years in public speaking; 14 years in quality/six sigma; 4 years in IRB administration
Topics:
IRB software; informed consent; adverse events; quality/six sigma

USA - Tennessee - Knoxville
Barbara Munsey BS
Director, Oncology Clinical Trials
University Health System
Telephone: +1 (865) 305-7136.
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Experience:
15+ Years in oncology clinical research as regulatory coordinator, study coordinator, scientific peer review committee coordinator, and research director
Topics:
Oncology research; clinical trial department implementation and operations; budget development; informed consent; recruitment challenges; how to keep current in oncology research

USA - Tennessee - Memphis
Amy M. Doville MBA CCRP
Director, Central Protocol and Data Monitoring Office
St. Jude Children's Research Hospital
Telephone: +1 (901) 495-3701.
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Experience:
20 years in medical and consumer research; 10 years in clinical research
Topics:
Clinical research education; GCP; monitoring; investigator responsibilities; human subjects protection
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