Administrative - Clinical Research Coordinator

ICONMA, LLC
  • Orange, CA
  • $40–$42 Per Hour
  • Instant Apply
2 days ago

Job Description

Our Client, a Healthcare company, is looking for a Clinical Research Coordinator - Hybrid job for their Orange, CA location.
 
Responsibilities:
  • Reads and understands all correspondence relating to each study assigned. Responsible for all written and verbal communication and the documentation thereof. This will include but not be limited to communications with study sponsors, monitors, study subjects/patients, physicians and laboratories or other study-specified service providers.
  • Responsible for all IP accountability specific to each subject and total protocol inventory. Role includes proper documentation of IP assignment, temperature and expiration date monitoring, return of used IP, and destruction or return to sponsor.
  • Works with subjects/patients to ensure study compliance and understanding of participation requirements (i.e., timeliness of visits, return of study-related materials and at-home documentation.
  • Complete, accurate and timely entry (within 7 days of visit) of visit data into study electronic data capture sites when applicable.
  • Recruits and retains study Participants.
  • Processes, packages, and ships biological samples as required by study or centralized laboratories.
  • Organizes and maintains study binders for each participant in a study. Ensures that filing is complete, accurate and consistent among study participants.
  • Attends investigators’ meetings as required.
  • Works with patients to ensure that study requirements are met including appointments, labs, etc.
  • Networks and researches potential new studies.
  • Performs regulatory functions for existing studies.
  • Maintains control over study medications/supplies.
 
Requirements:
  • Prefer to have a minimum of two years of experience in a Clinical Research setting where coordinator managed patients.
  • Cardiology/Stroke specialty a plus.
  • Device trial experience will not be accepted. Solely data trials experience also not accepted.
  • Minimum 2 years experience in a clinical research setting where candidate managed patients (consent them, perform vitals/EKG, process labs, dispense medication, complete documentation, enter data)
  • Must Have Epic Experience
  • Must also have strong computer skills - Outlook, MS Teams, Word, Excel
 
Why Should You Apply?Excellent growth and advancement opportunities
#mcbWhy Should You Apply?

Numbers & Facts

LocationOrange, CA
Salary$40–$42 Per Hour

Skills

  • Cardiologyunmatched
  • Cerebral Vascular Accidentunmatched
  • Clinical Researchunmatched
  • Computer Skillsunmatched
  • Data Entryunmatched
  • Documentationunmatched
  • Electrocardiogramunmatched
  • Health Planunmatched
  • Healthcareunmatched
  • IP (Internet Protocol)unmatched
  • Laboratoryunmatched
  • Maintain Complianceunmatched
  • Medicationsunmatched
  • Microsoft Excelunmatched
  • Microsoft Outlookunmatched
  • Microsoft Wordunmatched
  • Organizational Skillsunmatched
  • Presentation/Verbal Skillsunmatched
  • Regulationsunmatched

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