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Clinical Research Assistant II

Job in Royal Oak - Oakland County - MI Michigan - USA , 48073
Company: Beaumont Hospital, Royal Oak (Mich.)
Contract position
Listed on 2021-02-24
Job specializations:
  • Healthcare
  • Research/Development
    Clinical Research, Research Assistant
Job Description & How to Apply Below
GENERAL SUMMARY:


The Clinical Research Assistant II will assist the clinical research coordinator and/or research nurse in the conduct of clinical research trials, including basic patient screening, consenting for appropriate studies, data entry, specimen collection, processing and shipping.


ESSENTIAL DUTIES:


  • Assist research team with research study (basic patient screening/looking up patient data, complete CRFs, patient logs, clinical data collection [vital statistics], etc.) With appropriate oversight and specific training, may perform phlebotomy, collect clinical data (ex. vital signs) and assist with basic regulatory document preparation.
  • Word processing (data entry, spreadsheets, patient logs).
  • Specimen processing and shipping.
  • Interface with sponsor and review CRFs with sponsor with oversight.
  • Practice BH hospitality standards.
  • Consent and conduct research visits for data collection/no risk trials with oversight as appropriate.
  • Communicate effectively with subject, research team, Principal Investigators, and sponsors. Protect patient confidentiality.
  • Implement quality controls and assurance methods.
  • professional and technical knowledge.



  • STANDARD QUALIFICATIONS

    • High School Diploma or equivalent.
    • Must be either Research Certified (SoCRA or ACRP) with two years clinical research experience or Certified EMT, Certified Phlebotomist, or a Certified Medical Assistant with three years relevant direct patient care experience including vitals, patient interviews, etc.
    • Research certification (SoCRA or ACRP) required within 2-5 years of hire. BLS certification required.
    • Knowledge of FDA guidelines and Good Clinical Practices (GCP) guidelines preferred. If applicable, department-specific certification and/or experience may also be required. Phlebotomy skills prior to hire strongly preferred.MS Word required. Effective communication skills. Excellent organizational skills. Knowledge of FDA Regulations, Good Clinical Practices (GCP) guidelines.
    • Phlebotomy skills prior to hire strongly preferred.
  • CKNOWLEDGEMENT OF EMPLOYMENT UNDER RESEARCH GRANT
  • Position Requirements
    Less than 1 Year work experience
     
     
     
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