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DCRI - Clinical Research Associate Resume Example

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XXX XXXXXXXXXX XXXXX, CANA, VA 24317
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Ph: XXXXXXXXXX
Nathan Gonzalez
Professional Summary

Responsible registered nurse,  proficient in Phlebotomy  and nursing . Passionate and motivated, with a drive for excellence. 30 years combined in Plasma Center and nursing positions.

Skills
  • Active Listening
  • Coordination
  • Reading Comprehension
  • Writing
  • Medicine and Dentistry
  • English Language
  • Speaking
  • Administration and Management
  • Critical Thinking
  • Judgment and Decision Making
  • Management of Personnel Resources
  • Monitoring
  • Time Management
  • Active Learning
  • Complex Problem Solving
  • Mathematics
  • Biology
  • Science
  • Chemistry
Experience
Clinical Research Associate Aug 2010Jun 2014 DCRI Durham, NC
  • Managed the development, coordination and implementation of clinical operations, site management and clinical monitoring responsibilities for assigned projects with guidance, including trial specific processes and systems, and daily supervision of the Clinical Operations team. 
  • Monitor study activities to ensure compliance with protocols and with all relevant local, federal, and state regulatory and institutional polices.
  • Assess eligibility of potential subjects through methods such as screening interviews, reviews of medical records, and discussions with physicians and nurses.
  • Prepare for or participate in quality assurance audits conducted by study sponsors, federal agencies, or specially designated review groups.
  • Identify protocol problems, inform investigators of problems, or assist in problem resolution efforts such as protocol revisions.
  • Prepare study-related documentation such as protocol worksheets, procedural manuals, adverse event reports, institutional review board documents, and progress reports.
  • Track enrollment status of subjects and document dropout information such as dropout causes and subject contact efforts.
  • Review proposed study protocols to evaluate factors such as sample collection processes, data management plans, and potential subject risks.
Clinical Team Manager Nov 1998Sep 2009 PPD Morrisville , NC


  • Maintain required records of study activity including case report forms, drug dispensation records, or regulatory forms.
  • Oversee subject enrollment to ensure that informed consent is properly obtained and documented.
  • Schedule subjects for appointments, procedures, or inpatient stays as required by study protocols.
  • Monitor study activities to ensure compliance with protocols and with all relevant local, federal, and state regulatory and institutional polices.
  • Perform specific protocol procedures such as interviewing subjects, taking vital signs, and performing electrocardiograms.
  • Record adverse event and side effect data and confer with investigators regarding the reporting of events to oversight agencies.
  • Assess eligibility of potential subjects through methods such as screening interviews, reviews of medical records, and discussions with physicians and nurses.
  • Participate in preparation and management of research budgets and monetary disbursements.
  • Interpret protocols and advise treating physicians on appropriate dosage modifications or treatment calculations based on patient characteristics.
  • Review scientific literature, participate in continuing education activities, or attend conferences and seminars to maintain current knowledge of clinical studies affairs and issues.
  • Contact industry representatives to ensure equipment and software specifications necessary for successful study completion.
Physician Substitute Apr 1993Nov 1998 Sera Care Plasma Raleigh , NC
  • Conduct chemical analyses of body fluids, such as blood or urine, using microscope or automatic analyzer to detect abnormalities or diseases and enter findings into computer.
  • Conduct blood tests for transfusion purposes and perform blood counts.
  • Set up, maintain, calibrate, clean, and test sterility of medical laboratory equipment.
  • Collect blood or tissue samples from patients, observing principles of asepsis to obtain blood sample.
  • Analyze the results of tests or experiments to ensure conformity to specifications, using special mechanical or electrical devices.
  • Supervise or instruct other technicians or laboratory assistants.
  • Inspected facility and evaluated employees for compliance with CPR, OSHA and company SOP'S. 
  • Monitored donors for adverse reactions, company SOP's OSHA and federal regulations. 
Education
Registered Nurse: Nursing May 1986 Pikes Peak Community College Colorado Springs , CO
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Resume Details

This is a real resume for a Clinical Research Associate in CANA, Virginia with experience working for such companies as Dcri, Ppd, Sera Care Plasma. This is one of the hundreds of Clinical Research Associate resumes available on our site for free. Use these resumes as templates to get help creating the best Clinical Research Associate resume.

Previous Companies:

  • DCRI
  • PPD
  • Sera Care Plasma

Previous Job Positions:

  • Clinical Research Associate
  • Clinical Team Manager
  • Physician Substitute

Schools:

  • Pikes Peak Community College

Level of Education:

  • Registered Nurse

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