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Clinical Research Coordinator Resume Example

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CLINICAL RESEARCH COORDINATOR
Professional Summary
Responsible LPN with excellent communication skills demonstrated by 20 years of experience in healthcare. Accredited Clinical Research Coordinator with over 10 years of experience in the ares of Oncology, Alzheimer disease and Pain Management
Skill Highlights
Research and Analysis Computerized charting specialist Data QC and Integrity Medical clinical procedures comprehension Critical Thinking Problem resolution ability Extensive Organizational Skills
Professional Experience
05/2016
Clinical Research Coordinator Compass Research － The Villages, FL
  • Coordinate clinical research trials in the areas of Alzheimer's Disease and Pain Management. 
  • Coordinate multi-site or large-scale clinical trials research studies conducted by a supervising principal investigator(s) in support of activities that meet objectives of assigned research protocol(s).
  • Assesses patients for protocol eligibility and communicates findings to investigator/physician.
  • Coordinates the implementation of protocol procedures.Operates specialized equipment as needed in assigned area, if applicable.
  • Assesses and monitors patient responses and adverse reactions; reports same to accountable sources.
05/2016
Oncology Abstractor Flatiron － New York City, NY
Oncology abstrating in the areas of Breast Cancer, Colorectal Cancer, Non-Small Cell Lung Cancer. 
  • Ability to work remotely
  • Understanding of QC/QA processes
  • Spotlight Team Member 
  • High level of understanding of Patient Manger workings
  • Fluent in medical terminolgy
  • Ensured HIPAA compliance.
​
09/2015 to 05/2016
CRA GeNO LLC － Cocoa, FL
  • Assist in investigator study selection and start-up.
  • Create clinical project documents according to the protocol, including but not limited to, source documents forms and guidelines, instructions on use, monitoring visit templates and reports.
  • Identify site issues and coordinate corrective action plans based on needs.
  • Writing of Standard Operating Procedures based on local and federal requirements with the FDA and ICH guidelines.
  • Create and utilize Site Payment Database for accurate and timely study specific payments.
  • Team Leader for implementation of new study database including UAT, data entry and data transfer for interim analysis.
  • Ensure Adverse Events are reported appropriately, accurately and in a timely manner.
  • Mange Site Master File contents and work with sites to ensure communication requirements between site and IRB are adhered to.
  • Review CRF, Informed Consent Documents and query language/narratives.
11/2007 to 09/2015
Clinical Research Coordinator II UF Health Cancer Center Orlando Health － Orlando, FL
  • Melanoma, Sarcoma and Phase I.
  • Coordinate multi-site or large-scale clinical trials research studies conducted by a supervising principal investigator(s) in support of activities that meet objectives of assigned research protocol(s).
  • Coordinate clinical trials for Industry sponsored, Cooperative Groups- SWOG, GOG, COG and NRG.
  • Assesses patients for protocol eligibility and communicates findings to investigator/physician.
  • Coordinates the implementation of protocol procedures.
  • Operates specialized equipment as needed in assigned area, if applicable.
  • Assesses and monitors patient responses and adverse reactions; reports same to accountable sources.
  • Provides appropriate patient and family education.
  • Completes a variety of reports, documents and correspondence for regulatory agencies, participating clinical trial sites and for internal purposes.
  • Collaborates with physicians and other healthcare staff to ensure adherence to FDA and protocol guidelines; identify potential problems and/or inconsistencies and take action as appropriate.
  • Assist in the preparation and submission of amendments to clinical trials protocols to the IRB.
  • Provides educational in-services as needed.
  • Promotes interdepartmental cooperation and coordination for each protocol.
  • Maintains reasonably regular, punctual attendance consistent with Orlando Health policies, the ADA, FMLA and other federal, state and local standards.
  • Maintains compliance with all Orlando Health policies and procedures.
03/2006 to 10/2006
Clinical Research Coordinator Orlando Clinical Research Center － Orlando, FL
  • Obtaining and documenting Informed Consent per Good Clinical.
  • Practice.
  • Completing CRFs both paper and electronic with accuracy.
  • Creating source documents for Phase I and Phase II studies.
02/2004 to 11/2007
Dosing Nurse Orlando Methadone Treatment Center － Orlando, FL
  • Monitor patient responses to treatment and side effects.
  • Educate patient regarding side effects and correct treatment schedule.
Education and Training
2017
Western Governor's University － Salt Lake City, FL, United States
Lively Technical Center － Tallahassee, FL, United States
Associate of Arts: Liberal Arts Valenica Community College － Orlando, FL, USA Liberal Arts
Professional Affiliations
Licensed Practical Nurse - Florida - PN5156202 SoCRA - Member ID - 34034 ONS- Member ID - 355996
Interests
Basic Life Support (BLS) Certification 2007 Licensed Practical Nurse in the State of FL, License number PN5156202 to present
Skills
ADA, clinical trials, Critical Thinking, data entry, data transfer, Database, forms, Team Leader, monitors, Organizational Skills, policies, Problem resolution, protocols, Research, supervising
Additional Information
  • Licenses Basic Life Support (BLS) Certification 2007
  • Licensed Practical Nurse in the State of FL, License number PN5156202 to present
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Resume Overview

Companies Worked For:

  • Compass Research
  • Flatiron
  • CRA GeNO LLC
  • UF Health Cancer Center Orlando Health
  • Orlando Clinical Research Center
  • Orlando Methadone Treatment Center

School Attended

  • Western Governor's University
  • Lively Technical Center
  • Valenica Community College

Job Titles Held:

  • Clinical Research Coordinator
  • Oncology Abstractor
  • Clinical Research Coordinator II
  • Dosing Nurse

Degrees


  • Associate of Arts : Liberal Arts

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