Mildred Peets - Clinical Research Coordinator Resume Simple
Clinical research coordinator with experience in phase II, III, and IV certified. I have extensive experience in the pharmaceutical industry. I have worked in the areas of study and research as a clinical research coordinator.
  • scheduling, documentation, drafting, administrative, patient, database, budgets, administrative tasks, ekgs, vitals
  • 2017-12-252017-12-25

    Clinical Research Coordinator

    Nordstrom Inc

    • Conduct EKGs, vitals, and blood draws. Perform ECG's, urine drug screens, and file. Maintain database.
    • Maintain accurate and complete records of study activities, including but not limited to, patient enrollment, participant screening, source documentation, data entry, and maintenance of study files.
    • Perform administrative duties such as answering the phone, scheduling appointments, and maintaining study files. Assist with the preparation of IRB submissions.
    • Maintain a detailed and accurate records of study budgets, including drafting and editing of posters, and meeting minutes.
    • Manage and maintain all regulatory documents for the clinical trials. Provide guidance to the study team to ensure proper protocol adherence.
    • Perform all administrative tasks such as photocopying, organizing and preparing documents. Ensure that all study documents are complete and accurate.

 CTP Enterprises