TI Clinical Research Assistant

Job Listing ID:

4488326

Job Title:

TI Clinical Research Assistant Application Deadline:

Open Until Filled

Job Location:

Portland

Date Posted:

05/08/2026

Hours Worked Per Week:

40

Shift:

Day Shift Duration of Job:

Either Full or Part Time, more than 6 months You may contact this employer directly. (Obtain the contact information to print or add to your jobs.)

Job Summary:

TI Clinical Research Assistant US-OR-Portland Requisition ID:

2026-39140

Position Category:

Research

Job Type:

Research

Position Type:

Regular Full-Time

Posting Department:

Neurology

Posting Salary Range:

$23.43 - $37.27

Posting FTE:

1.00

Posting Schedule:

M-F

Posting Hours:

8:00am- 4:30pm

HR Mission:

School of Medicine

Drug Testable:

Yes Department Overview Therapeutic Intervention Clinical Research Assistant position in the Department of Neurology. Responsible for coordinating multiple complex therapeutic interventional trials while adhering to study protocol timelines and working closely with Principal Investigator to ensure participant safety. •Please include a cover letter with your application and resume.

Function/Duties of Position Recruitment & Retention:

recruitment of research volunteers by determining interest and eligibility in accordance with study protocol; explaining complex study design and procedures in lay language to potential participants; creating recruitment materials; screening and enrolling eligible participants, and retaining participants for duration of the study protocol.

Study Coordination:

coordinate scheduling, preparation, and conduct of complex study visits involving multiple staff and hospital services; assure completion of study assessments and procedures per protocol; obtain informed consent; collect, process, store, and ship laboratory samples; conduct and/or assist with study procedures such as collection of vital signs, ECGs, lumbar punctures, & skin punch biopsies. Assist Clinical Trials Manager in tracking and reviewing study billing, including review of hospital charges and tracking invoiceable assessments and procedures. Effective and professional communication (written / electronic and verbal) with study team, study participants, sponsors, contract research organizations (CRO), investigators, local and central Institutional Review Boards (IRBs), and other departments at OHSU. Preparation for and coordination of monitoring visits by CRO and federal agency representatives.

Regulatory document maintenance:

ongoing maintenance of regulatory compliance and organization of all study documents and materials, adhering to Good Clinical Practice guidelines; assist with regulatory submissions to IRB, including initial submission, modifications, and annual reviews.

Data Entry:

timely, accurate completion of all required case report forms during study visits; entry of data into electronic data capture systems within sponsor-required timelines; timely resolution to data queries issued by sponsor and/or study monitor.

Additional Support:

serve as trained, back-up study coordinator for other trials within the Movement Disorders Divis Equal employment opportunity, including veterans and individuals with disabilities.

PI284378090

Job Classification:

Natural Sciences Managers Access our statewide or regional occupation report for more information about wages, employment outlooks, skills, training programs, related occupations, and more. Compensation

Salary:

Not Provided Job Requirements

Experience Required:

 At least 1 year

Education Required:

High School Diploma/GED

Minimum Age:

N/A Gender:

N/A