TI Clinical Research Assistant 2 at Oregon Health & Science University in Portland, Oregon

Job Description:

Oregon Health & Science University

Oregon Health & Science University values a diverse and culturally competent workforce. We are proud of our commitment to being an equal opportunity, affirmative action organization that does not discriminate against applicants on the basis of any protected class status, including disability status and protected veteran status. Individuals with diverse backgrounds and those who promote diversity and a culture of inclusion are encouraged to apply. To request reasonable accommodation contact the Affirmative Action and Equal Opportunity Department at 503-494-5148 or aaeo@ohsu.edu.


TI Clinical Research Assistant 2

US-OR-Portland

Job ID: 2025-33618
Type: Regular Full-Time
# of Openings: 1
Category: Research
Portland, OR (Marquam Hill)

Overview

Layton Center clinical trials team Clinical Research Coordinators (TI Clinical Research Assistant 2) are highly organized and are responsible for duties related to the implementation of  human subject research protocols. Clinical Research Coordinators must effectively and professionally communicate (verbally including by phone and video call as well as in writing) within the Layton Center clinical trials team, with many other departments at OHSU, with study sponsors and contract research organizations (CROs), with vendors, and with study participants/volunteers. 

 

Clinical Trial Coordination 

• Recruiting, screening, consenting, and enrolling eligible participants/volunteers for interventional and observational clinical trials.
• Preparing for and coordinating in-person study visits including scheduling of study participants/volunteers, study staff (including physicians and nurses), of clinic space, infusion appointments, and/or imaging appointments under general supervision.
• Coordinating with OHSU research pharmacies and assisting with intervention administration.
• Assisting with and/or administration of neurocognitive assessments/tests.
• Collection and entry of study data on case report forms (CRFs).
• Collecting vital signs and blood; Performing EKGs/ECGs.
• Collection and timely reporting of adverse event (AE) data to study sponsors and Institutional Review Boards (IRBs).
• Data entry into study-specific databases and clinical trial electronic data capture (EDC) systems; Responding to EDC queries.
• Collection, processing, storage, and/or shipment of biologic samples (such as blood, urine, and cerebrospinal fluid); Study visit supply organization, inventory checks, and ordering.
• Maintaining communication with study participants/volunteers throughout the trial and follow up period.
• Collaboration with the clinical research billing office to ensure accuracy and completeness. 
• Assisting with routine correspondence with the OHSU IRB and industry sponsor IRBs related to required submissions, protocol modifications, and continuing reviews.
• Assisting with regulatory document and binder maintenance in compliance with Good Clinical Practice (GCP) standards.
• Ensuring compliance with all protocol and regulatory requirements.
• Recognition of, documentation of, and communication about protocol deviations within sponsor and institutional guidelines.
• Attending, actively participating in, and providing updates at recurring Layton Center clinical trials team meetings.
• Ensuring that required Collaborative Institutional Training Initiative (CITI) program trainings are complete, up to date, and renewed in a timely manner.
• Must be willing and able serve as a backup for other Layton Center clinical trials Clinical Research Coordinators (Clinical Research Assistants) to provide coverage for time off.
• May assist with onboarding and training of other staff as needed to ensure study participant safety and study continuity

Responsibilities

• Bachelor’s degree in relevant field; OR Associate’s degree AND 2 years of relevant experience; OR 3 years of relevant experience; OR Equivalent combination of training and experience.
• Working knowledge of scientific methods and human subjects research
• Intermediate or advanced knowledge of Word, Excel, Outlook, and other MS Office programs
• Demonstration of high level of attention to detail; self-starter; ability to prioritize work demands and manage time appropriately
• Demonstrated high level of organization and ability to efficiently manage multiple tasks 
• Ability to speak and communicate clearly and demonstrate a high level of professionalism; ability to interact patiently and respectfully with elderly volunteers
• Able to perform the essential functions of the position with or without accommodation
• Must possess excellent written and verbal communication skills

Qualifications

• Clinical research coordination experience preferred
• Clinical trial experience preferred 
• Experience with Epic or other electronic medical records systems(s)
• Clinical skills including phlebotomy, specimen processing, ECG and vitals measurement, and/or neurocognitive test administration
• Experience working with seniors

Equal employment opportunity, including veterans and individuals with disabilities.

PI265936543

Salary:

$46.00

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