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The sample below is for a Clinical Research Project Management Resume. This resume was written by a ResumeMyCareer professional resume writer, and demonstrates how a resume for a Clinical Research Project Management Candidate should be properly created. Our Certified Professional Resume Writers can assist you in creating a professional document for the job or industry of your choice.

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CLINICAL RESEARCH

Multifaceted and service focused professional with a valuable track record in various functions in medical diagnostics, hospital and patient care. Highly organized and performance driven with strong educational foundation and extensive experience in the clinical research and development field. Highly reliable and dedicated in providing compassion, care and assistance to those who require emergency intervention with in-depth knowledge of health care principles, techniques, and hospital operations. An excellent communicator coupled with strong interpersonal skills, effective in nurturing positive relationships with patients, staff, and individuals at any level or background.

Core Competencies
Project Management • Research Monitoring & Management • Medical Diagnostics • Patient Care/Health Administration
• Patient Assessment • Medication & Rehabilitation • Physical Examination/Patient Assessment

PROFESSIONAL EXPERIENCE

Emory Winship Cancer Institute Clinical Trials Office • Atlanta, GA 2009 – Present
Clinical Research Coordinator III
Carry out oncology trials in compliance with institutional policies, SOPs and GCP guidelines. Interface with research participants and study sponsors throughout all phases of the study. Manage and review clinical research trails’ data, systems, and outcomes. Closely monitor IRB submissions and respond to requests and questions.
• Served on steering committees for improving research at Emory, orientation, and staff appreciation.

Emory Winship Cancer Institute Clinical Trials Office • Atlanta, GA 6 months
Associate Director Clinical Trial (Interim)
Managed 40 clinical research coordinators I-III and research registered nurses. Worked with staff and team leads to establish work plans, goals and objectives. Assisted in site preparation for FDA audits, accreditation visits, and inspections. Supported physicians during Grand Rounds to discuss changes in departmental SOPs.
• Contributed to the development of merit promotion system, and performance metrics for individuals and teams. Established and developed department’s first official orientation program.
• Proposed a new system to easily track individual effort on studies to ensure grants were charged appropriately. Streamlined documentation process through development of departmental forms.

Vanderbilt University Hospital Ingram Cancer Center • Atlanta, GA 2001 – 2003
Clinical Trials Associate
Oversaw participants for cooperative oncology clinical trial studies. Conducted audits at research hospitals, and developed promotional material for a National Sibling Trial. Developed SOP for clinical trials.
• Received training in medical terminology, IRB procedures, and interpretation of medical reports.

OTHER EXPERIENCES
Officer (Rank- Lieutenant Colonel) United States Army Reserve • (Veteran) 1992 – Present
Education Program Manager Baptist Hospital Center for Health and Wellness • Nashville, TN

EDUCATION AND CREDENTIALS

UNIVERSITY OF TENNESSEE – Knoxville, TN
Master of Science Health Education and Health Promotions, 1996
Bachelor of Science in Biology, 1991

TRAINING/CERTIFICATIONS
18 graduate level credit hours towards a Master of Science in Military Arts and Science, 2011
US Army Combine Arms Training Center – United States of America

TECHNICAL SKILLS
Microsoft Office Suite: Word, Excel, PowerPoint, Outlook;
Powerchart; Oracle; Rave; Advantage; EPIC; IDX; IVRS; Inform; Meta Data

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