SharÛn W. Scott, CCRA

Careers In Research, Inc.

203 Brandon Drive

Clayton, NC 27520

919-550-3385 Home  919-550-8411 Bus.

careers.inc@mindspring.com

 

Qualifications

 

                Senior CRA - Experience with but not limited to identifying and recruiting qualified investigators, site evaluation visits, initiation visits, interim monitoring visits and termination visits; leading multiple project teams, training investigators and site personnel on specific project tasks, including recruitment strategies, protocol procedures, SAE reporting, compliance and FDA audit preparation, and drug accountability.

                Therapeutic areas of experience include the following: CNS - including Alzheimerís disease, depression; Cardiovascular - hyperlipidemia, intermittent claudication, CHF, hypertension, nutrition; Respiratory - asthma, COPD; Endocrinology/hepatic - renal transplant, diabetes; Infectious Diseases ñ influenza; Orthopedic - osteoarthritis, osteoporosis, pain management; Oncology - prostate cancer, breast cancer; Gastroenterology - gastric ulcer, IBS, GERD ñ adult and pediatric; Neurology - stroke, epilepsy ñ infant and adult

                Study Coordinator 3 years - responsible for all aspects of study conduct including IRB submissions, patient scheduling and enrollment, spirometry, ECGs, patient home visits, etc.

                Excellent computer and inter-personal skills, effective teacher/trainer with over 9 years experience coordinating task accomplishments and working with a diverse range of personalities

 

Professional Experience

 

                Consultant for various pharmaceutical companies and CROs since 1998

                Proficient computer skills for writing monitoring reports, telephone contact reports, data queries, confirmation and follow-up letters, investigator databases, regulatory document and enrollment tracking, source document worksheet development and CRF development using Microsoft windows 97, 98, 2000 in Excel, Access, Word and other computer systems

                All aspects of field monitoring from investigator recruitment to territory development in both CRO and sponsor environments since 1995

 

Management and Training

 

                Supervised, trained and co-monitored with new CRAs since 1996

                Edited and corrected monitoring reports prior to submission to management/sponsor

                Lead CRA roles, including regulatory document, CRF and site visit tracking

 

Education

 

                BS in Psychology, University of California, Davis ñ Core science curriculum

                Effective Leadership and Communication skills - continuing education credits annually

 

Professional Affiliations

 

                Current member of ACRP and DIA