Alzheimer's Clinical Research Assistant - Data Entry

Rush University Medical Center

Chicago (IL)

Vor Ort

USD 25.000 - 34.000

Vollzeit

14 Tage+

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Zusammenfassung

Rush University Medical Center is seeking a Clinical Research Assistant in the Rush Alzheimer’s Disease Center-Research Facility. The role involves data collection and documentation for clinical studies, with potential evening, overnight, and weekend hours as protocols require.

The candidate will assist with data entry, participant eligibility, scheduling, and coordination with a multi-disciplinary team while maintaining confidentiality and meeting deadlines in a fast-paced research environment.

Qualifikationen

  • High School Diploma is required.
  • 1 year of experience with data collection.
  • Entry level proficiency in Microsoft Office, including spreadsheets and databases.
  • Ability to meet deadlines.
  • Detail oriented with high attention to accuracy.
  • Ability to maintain confidentiality with a diverse pool of research participants.

Aufgaben

  • Administers tests and questionnaires including eligibility assessment per study protocols.
  • Assist with recruitment, screening and scheduling potential study participants.
  • Collect and enter data into study case report forms or EDC systems.
  • Respond to queries in a timely manner; assist with document submission to IRB as needed.
  • Maintain accurate documentation of consent, HIPAA forms, IRB approvals, and study communications.
  • Gather materials for participant visits and assist with data analysis and reporting.

Kenntnisse

Data collection
Data entry
Microsoft Office
Attention to detail
Verbal and written communication
Ability to meet deadlines
Confidentiality

Ausbildung

High School Diploma
Bachelor’s degree in Sciences or health-related discipline

Tools

Electronic Data Capture (EDC) system

Jobbeschreibung

Rush University Medical Center is seeking a Clinical Research Assistant in the Rush Alzheimer’s Disease Center-Research Facility. The role involves data collection and documentation for clinical studies, with potential evening, overnight, and weekend hours as protocols require.

The candidate will assist with data entry, participant eligibility, scheduling, and coordination with a multi-disciplinary team while maintaining confidentiality and meeting deadlines in a fast-paced research environment.

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