Candidate Information | Title | Clinical Research Coordinator | Target Location | US-PA-Philadelphia | Phone | Available with paid plan | | 20,000+ Fresh Resumes Monthly | |
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| | Click here or scroll down to respond to this candidateEdith Fletcher RN, BSNPHONE NUMBER AVAILABLEEducational HistoryStreet Address 1993 Fitchburg State University, Fitchburg MA (BSN) GPA 3.84Street Address 1990 Delaware County Community College Media, PA (ADN)Licenses and CertificationsTemporary Covid-19 Emergency New Jersey License for Out-of-State PractitionerrLicense# NJOCATEMP012494Board of Nursing, State of California#RN507779 (Active)Board of Nursing, State of Pennsylvania#RN593211 (Active)American Heart Association /BLS Certification (1990 Present)ACRP Certified Clinical Research Coordinator (Nov 1998 2013)UPENN Certified Clinical Research Coordinator (Sep 2013 Nov 2017)NIH CITI Certification Protection of Human Subjects in Clinical Trials ActiveEmployment HistoryMay 2020 - Present Per-Diem RN Elite Medical Staffing LTC Facility Covid-19 Patient Care2019 - 2020. Clinical Research Coordinator/GastroenterologyHillmont GI, Flourtown PennsylvaniaManagement of all aspects of Clinical Trials from start-up to completion of the trails. Ensure patient compliance per protocol. Reporting Adverse events to physicians and study sponsors and continued patient follow-up.2016 2017 Clinical Research Coordinator/OncologyCity of Hope, Duarte CaliforniaManaged all aspects of Oncology research projects (Phase I-IV). Patient Recruitment/Retention in clinical trials from enrollment to completion of trial. Ensure patient compliance with research protocols. Patient assessments and reporting of any adverse events to physicians. Provided orientation on the research protocols to the nursing staff administering study medication.2013 2016 Clinical Research Coordinator/Interventional Cardiology of Pennsylvania, Hospital of the University of Pennsylvania, Philadelphia PAManage Phase I-IV clinical trials from site selection to closing including, but not limited to; IRB Submissions, Budget Preparation, Training of Physicians and Staff on protocol adherence, site initiations, and implementation of new protocols.2012 Clinical Research Coordinator/CardiologyClinlogix, Inc. On-Site at Abington Hospital/Cardiology Group, Abington, PACoordinated and implemented Phase I-IV Clinical Trials. Handles patient Recruitment/Retention, IRB submissions and Consent reviews/Revisions. Performed ECGs, Blood draws and Lab processing and shipping. Consulted on budget and contracts for studies worked on. Verified patient eligibility, submitted all data and maintained all regulatory requirements.2009 Present Independent Clinical Research ConsultantCoast2Coast Research Consulting, Inc. Self-EmployedContract work for Clinical Sites, Pharmaceutical & Biotech Companies, including but not limited to; Contract and Budget negotiations, Protocol Reviews, IRB submissions and Consent Revisions. Worked as Clinical Site Coordinator and handling patient recruitment/retention.2003 2009 Lead Clinical Research Coordinator/Manager CardiologyCardiovascular Consultants Medical Group Oakland, CASuccessfully lead all aspects of research projects and research staff in Phase I-IV device and pharmaceutical trials with 21 Cardiologists, 5 sites and affiliated with 8 Hospitals. Handled Regulatory Submissions/IRB applications, Amendments and Consents. Secured contracts with Pharmaceutical & Biotech Companies. Developed and implemented SOPs for research department. Budgeted and worked in accounting management/negotiations. Worked on patient recruitment/retention (Phase I-IV with over 1000 patients enrolled)2001 2003 Clinical Research Coordinator/Lead InfertilityReproductive Science Center of the San Francisco Bay Area, San Ramon CAManaged all aspects of research projects (Phase I-IV). Handled Regulatory Submissions/IRB applications, Amendments and Consents. Secured contracts with Pharmaceutical & Biotech Companies. Developed and implemented SOPs for research department. Budgeted and worked in accounting management/negotiations. Worked on patient recruitment/retention (Phase I-IV).1991 - 2001 Clinical Research Coordinator/Lead Womens HealthLifeSpan Research, Palo Alto, CAManaged all aspects of research projects (Phase I-IV). Handled Regulatory Submissions/IRB applications, Amendments and Consents. Secured contracts with Pharmaceutical & Biotech Companies. Developed and implemented SOPs for research department. Budgeted and worked in accounting management/negotiations. Worked on patient recruitment/retention (Phase I-IV)1998 - 1999 Clinical Trials AdministratorACRC (AIDS Community Research Consortium) Redwood City, CAManaged all aspects of Multi-Site Clinical Trials in the SF Bay Area for HIV/AIDS Research. Managed all aspects of research projects (Phase I-IV). Handled Regulatory Submissions/IRB applications, Amendments and Consents. Secured contracts with Pharmaceutical & Biotech Companies.1996 - 1998 Clinical Research CoordinatorGood Samaritan Hospital San Jose, CADiagnostic Imaging Department: Coordinated and implemented Phase I-III Clinical Trials.1993 - 1995 Clinical Research Coordinator CardiologyCenter for Clinical and Lifestyle Research Shrewsbury, MACoordinated and Implemented Phase II-IV Clinical Trials. Performed Exercise Stress Testing including VO2 Max. Blood draws, processing and shipping specimens per HAZMAT policy.1990 - 1995 Registered Nurse: ICU/CCU Med/SurgClinton Hospital, Clinton, MAMed/Surg: 2 Years and ICU/CCU: 3 Years1988 - 1990 Nursing Assistant: Med/Surg UnitsAssisted RNs to provide quality patient care, while working on obtaining my nursing degree.PER DIEM POSITIONSRN Med/Surg Unit and Telemetry Unit, Valley Care Hospital, Leominster, MARegistry RN (ICU & Med/Surg) RNs Inc. Hayward, CAPUBLICATIONSE. Fletcher, K. Demers, J. Price, S. Damitz, L. Alquist, K. Stillwell, J. Rippe FASCM.Predication of Aerobic Capacity Before and After Exercise Using A Non-Exercise Model,Medicine and Science in Sports, Vol. 27:5, 1994. |