NCRA Principals

 NCRA BBB Business Review

Norwich Clinical Research Associates Ltd. (NCRA) principals are highly qualified in their fields with corresponding industry and/or academic experience and accomplishments. We have especially strong Clinical Consulting, Clinical Operations, Data Management, GCP Auditing, and communication expertise as well as specialized Scientific Writing skills.

 

 

Lee Truax-Bellows, M.S., FNP, CCRA, RQAP-GCP (View CV PDF)
President, CEOand Chairman of the Board

Lee Truax-Bellows is a Family Nurse Practitioner with an extensive background in the pharmaceutical and medical device industries, having worked for both industry and a CRO. She has been involved in regulated research since 1990. She is a founder, President and CEO of NCRA. Lee currently specializes in clinical product development, GCP auditing, SOP development and training, clinical Quality Management System (QMS) development and GCP training. She belongs to the Association of Clinical Research Professionals (ACRP), Model Agreements & Guidelines International (MAGI), the Medical Device Regulatory Working Group (MDRWG) and Society of Quality Assurance (SQA). She is an ACRP Certified Clinical Research Associate (CCRA), a Registered Quality Assurance Professional in GCPs under SQA (RQAP-GCP) and an Accredited Qualified Clinical Research Trainer (TIACR) under the International Academy of Clinical Research (IAOCR).

 

Glenda Guest, CCRA, RQAP-GCP (View CV PDF)
Vice Chairperson of the Board of Directors

Glenda Guest is a credentialed quality assurance auditor, clinical research associate and clinical trainer. She has been involved in regulated research since 1998 and specializes in GCP QA and third party auditing, medical device monitoring and project management,clinical Quality Management System (QMS) development and GCP training. Glenda is actively involved with and is designate as a Fellow of the Association of Clinical Research Professionals (FACRP). She has been an ACRP Certified Clinical Research Associate (CCRA) since April of 2002. She is a member the Society of Quality Assurance (SQA). She is designated by SQA as a Registered Quality Assurance Professional Good Clinical Practices (RQAP-GCP) since April 2007. She is an active volunteer with the Model Agreements and Guidelines International (MAGI) Medical Device Regulatory Working Group (MDRWG). She has attained Accredited Qualified Clinical Research Trainer (TIACR) designation via the International Academy of Clinical Research (IAOCR).

 

William Y.W. Au, M.D. (View CV PDF)
Medical Director
Clinical Pharmacology and Clinical Research
Professor of Medicine, Division of Clinical Pharmacology and General Medicine, SUNY Upstate Medical University, Syracuse, N.Y.

Dr Au is a specialist in clinical pharmacology and medical monitoring, endocrinology, metabolism and internal medicine. He has 21 years experience in the pharmaceutical and medical device industry. In addition he has 29 years in academia in clinical pharmacology, internal medicine, endocrinology, and metabolism research, teaching, and patient care.