Mary Edna Parish is a clinical research professional with over 15 years of experience in clinical trials. She has extensive experience in areas such as protocol development, regulatory compliance, patient recruitment, data collection and management, adverse event reporting, and project management. Her background includes positions as a clinical research coordinator at Le Bonheur Children's Hospital and St. Jude Children's Research Hospital, as well as a research nurse at Gastro One and the University of Tennessee Health Science Center. She has strong computer skills and is proficient in various clinical trial software programs and electronic medical records systems.

1. Mary Edna Parish, RN
4127 Callie Powell Cv Bartlett, TN 38135
901.734.5046 (c) • mepsplace@att.net
https://www.linkedin.com/in/maryednaparish
CLINICAL RESEARCH PROFESSINAL
Computer
• Proficient in MS Word, Excel, Powerpoint, PC, Internet, multiple Electronic Medical Records
(EMR) systems, iMedRIS Institutional Review Board (IRB) software, IntelliTrial (Clinical Trial
Management Sytem), multiple Electronic Data Entry (EDC) programs as well as paper data entry
Case Report Forms (CRFs), IVRS systems for randomization, drug dispensing, shipment
verification.
Key Strengths
• Compliance with DHHS and FDA guidelines, Good Clinical Practices, sponsor and institutional
guidelines
• Compliance with HIPAA guidelines
• IATA and CITI certified
• Completion and maintenance of regulatory
documentation
• Chart review and data abstraction
• Organization/management of workload
• Prioritizing tasks
• Research protocol budget negotiations
• Creation of source documentation
• Preparation of technical documents for
grants and professional publications
• Preparation of patient education material
Personal
• Detail Oriented
• Problem Solver
• Task and project oriented
• Effective team player
• Autonomous
• Multi-tasker
• Responsible
• Accurate
• Sense of humor
PROFESSIONAL EXPERIENCE
Clinical Research Coordinator positions all required the following:
• Attend Investigator meetings
• Create source documents
• Recruit patients via chart review, phone calls
• Review charts and abstract data
• Conduct Informed Consent process
• Maintain regulatory document binders
• Conduct patient visits according to protocol
guidelines
• Obtain and process lab specimens/ECGs
• Collaboration with other involved departments
• Prepare for and conduct monitor visits
• Calculate investigational product compliance
and accountability
• Promptly respond to sponsor queries
• Process Serious Adverse Event reports
• Conduct close-out procedures

2. Mary Edna Parish
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Clinical Research Coordinator, RN Le Bonheur Children’s Hospital 2012 to 2015
Areas of research: Neurology, Nephrology, Genetics
Clinical Research Nurse Gastro One 2012
Areas of research: Hepatitis C, Ulcerative Colitis, Crohn’s Disease
Clinical Research Associate I, RN St. Jude Children’s Research Hospital 2008 to 2011
Division of Anesthesiology
Performed all research related duties for both prospective and retrospective investigator-initiated
trials
Research Nurse Coordinator University of Tennessee Health Science Center 2005 – 2008
Research Coordinator Department of Neurology 2002 – 2004
Areas of research: Parkinson’s Disease, Restless Leg Syndrome
Negotiated budgets for sponsor contracts
Prepared and processed subcontracts for clinical research trials
Team member preparing and completing Annual Parkinson’s Disease Symposium
Research Consultant University of Tennessee Health Science Center 2004 – 2005
Department of Neurology
Area of research: Parkinson’s Disease
Independent consultant to Department of Neurology at the University of Tennessee
Prepared all regulatory documents and all IRB submissions for more complex protocol.
Registered Nurse (R.N.) Methodist HealthCare System 2004
Performed all aspects of total patient care in med-surg/telemetry hospital setting.
EDUCATION
Associate of Applied Science in Nursing, Southwest Tennessee Community College, Memphis, TN
Bachelor of Science in Special Education, Cum Laude, University of Tennessee, Knoxville, TN
PROFESSIONAL CERTIFICATES
Registered Nurse License - State of Tennessee #146243, Active
Certified Clinical Research Professional Certification, SoCRA, Expired Nov. 2015
Teaching License #524284 - State of Tennessee, Active
PROFESSIONAL ORGANIZATIONS
Society of Clinical Research Associates, Sept. 2009 to present
COMMITTEES
Mid-South SoCRA Chapter Conference Planning Committee, 2010 to 2011
Parkinson’s Study Group Budget Committee, 2008
Advisory Committee, West End Academy, Knoxville, TN, 2015 to present