TI Clinical Research Assistant II - Military veterans preferred

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 II

US-OR-Portland

Job ID: 2025-34067
Type: Regular Part-Time
# of Openings: 1
Category: Research
Portland, OR (Downtown)

Overview

• Assist the management of research study daily operations, monitoring protocol compliance and patient toxicities, adverse event reporting and regulatory submissions (IRB, FDA). May act as a project manager for specific protocols. Independently interact with study sponsors and provide all necessary documentation in a timely manner. Mentor junior staff on research protocols and provide support.
• Assist senior staff with database build and management, monitoring and issuing queries, performing analyses as needed, running reports, and presenting information to relevant stakeholders.
• Support new clinical trial start-up procedures though development of necessary regulatory documents to align with OHSU’s required template and language, develop visit schedule in OHSU’s CTMS, and provide additional support as needed.
• Complete special projects under the guidance of one of the group epidemiologists, including manuscript review, database support, etc.

• Bachelor's Degree in relevant field OR

• Associate's AND 2 years of relevant experience OR

• 3 years of relevant experience OR

• Equivalent combination of training and experience

• Strong written, verbal comminication and proficeincy in MS Office Suite; meticulous record keeping and organization skills.

• Working knowledge of IRB guidelines and FDA, DHHS, other agency guidelines that govern clinical research.

• Experience with EndNote or other citation software.

• Masters Degree in Public Health or currently working toward Masters Degree in Public Health 1-2 years of experience in clinical research including at least 1 year of clinical trial coordination
• REDCap database
• Familiarity with OHSU’s CTMS (eCRIS)
• Good Clinical Practice (GCP) Certification, SOCRA or ACRP Certification
• Phlebotomy training

PI269724429