Alzheimer’s Clinical Trials Coordinator

OHSU

Portland (OR)

Vor Ort

USD 55.000 - 75.000

Vollzeit

14 Tage+

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Zusammenfassung

The Layton Aging & Alzheimer's Disease Research Center at OHSU is seeking a Clinical Research Coordinator to support human subjects research protocols and coordinate study visits, data collection, and regulatory tasks. You will work within the Layton Center clinical trials team across NIH-funded studies of dementia in older adults.

Responsibilities include recruiting and screening participants, coordinating visits and imaging, data entry, EKGs/ECGs, and ensuring compliance with GCP and IRB

Qualifikationen

  • Bachelor’s degree or equivalent required for the role.
  • Experience with human subjects research and regulatory processes preferred.
  • Proficiency with Word, Excel, Outlook and MS Office suite.

Aufgaben

  • Coordinate human subject research protocols and study visits.
  • Recruit, screen, consent, and enroll participants for trials.
  • Prepare for visits including staff, space, and imaging coordination.
  • Collect and enter data in case report forms and CRFs.
  • Assist with regulatory documents and IRB submissions.
  • Communicate professionally with sponsors, CROs, and participants.

Kenntnisse

Scientific methods
MS Office
Attention to detail
Time management
Professional communication
Written communication

Ausbildung

Bachelor’s degree in relevant field
Associate’s degree + 2 years experience
3 years relevant experience
Equivalent combination of training and experience

Tools

Epic
EMR systems

Jobbeschreibung

The Layton Aging & Alzheimer's Disease Research Center at OHSU is seeking a Clinical Research Coordinator to support human subjects research protocols and coordinate study visits, data collection, and regulatory tasks. You will work within the Layton Center clinical trials team across NIH-funded studies of dementia in older adults.

Responsibilities include recruiting and screening participants, coordinating visits and imaging, data entry, EKGs/ECGs, and ensuring compliance with GCP and IRB

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