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 CoordinatorAltru Health System Clinic － Warroad , MN
- 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 AbstractorBickford Senior Living － Macomb , IL
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
Drug Information Association Inc － Cleveland , OH
- 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 IIAltru Health System Clinic － Erskine , MN
- 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 CoordinatorNew Season － Saint George , UT
- 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 NurseOrlando Methadone Treatment Center － City , STATE
- 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 － City, State, United States
Lively Technical Center － City, State, United States
Associate of Arts: Liberal ArtsValenica Community College － City, State, USALiberal 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
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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