Gary Richey - Clinical Research Coordinator Resume Simple
SUMMARY
To obtain a position as a clinical research coordinator in a reputable medical facility where I can utilize my skills and knowledge in the field of medicine.
SKILLS
  • analysis, implementation, documentation, communication, training, correspondence, research, collection, data collection
  • training, education, military, research, medical
WORK EXPERIENCES
  • 2017-12-252017-12-25

    Clinical Research Coordinator

    Westwood College

    • Duties include: recruitment, scheduling, data collection, documentation, and writing of study protocols. Assist in the development of protocols and reports.
    • Project Management: Study initiation, coordination, communication, and follow-up of study related activities, including but not limited to, protocol design, CRF completion, IRB submissions, protocol development, and collection.
    • Coordinates and conducts the implementation of study visits, including scheduling and follow-up of study related documentation. Prepares and submits regulatory documents.
    • Perform all aspects of research including but not limited to: Protocol preparation, data collection, study initiation, training, and scheduling of study participants.
    • Manage correspondence and reports for study analysis. Ensure that all regulatory documents are filed and archived. Assist in the preparation of IRB submissions.
    • Ensure that all study related activities are performed in compliance with the protocol, good clinical practice (GCP), and FDA regulations.
  • 2017-12-252017-12-25

    Clinical Research Coordinator

    Eastern Regional High School

    • Provided training and education to medical staff and students in the field of the military and civilian personnel. Trained and supervised new employees.
    • Performed all aspects of patient care including: Vital signs, phlebotomy, and specimen collection. Assisted with the preparation of specimens for testing.
    • Collect and analyze data for research purposes. Prepare and submit reports for sponsors. Prepare and submit grant proposals.
    • Assist in the preparation of medical charts, and other administrative duties. This includes but not limited to: Patient history, vital signs, and assisting with minor surgeries.
    • Maintains and organizes all study related documents and records. Performs quality control and assurance activities. Ensure compliance with regulatory agencies.
    • Clinical research Coordinator: Responsible for the management of all aspects of the study and the implementation of the electronic medical record (EMR).

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