About this opportunity
Oregon Health & Science University lists this TI Sr. Clinical Research Assistant (Clinical Research Coordinator) opportunity in portland, Oregon. Review the employer’s description below for duties, qualifications and application requirements.
Job description
TI Sr. Clinical Research Assistant (Clinical Research Coordinator)
Join to apply for the TI Sr. Clinical Research Assistant (Clinical Research Coordinator) role at Oregon Health & Science University
Pay Range
$50,128.00/yr – $75,171.20/yr
Department Overview
The mission of the Knight Clinical Research Management organization is to support the conduct of translational clinical research aimed at improving the lives of people and families with cancer by applying innovative strategies for cancer prevention, screening, diagnosis, and treatment. The support is provided through proactive, high‑quality, and efficient study management in compliance with federal regulations and local policies and procedures. This fast‑paced and highly intense research environment requires management of complex therapeutic interventional (TI) trials and clinical research studies involving a vulnerable and sick population.
Therapeutic Interventional (TI) Trials
Ti trials are treatment studies that involve people who have a disease or underlying condition. They include the administration and testing of new treatments or new ways of using existing treatments, such as new drugs, vaccines, or cell therapies.
Function / Duties of Position
Responsibilities
Working with the regulatory management team to complete all regulatory documentation in accordance with OHSU IRB and sponsor requirements
Creation of study trackers and organization tools
Assisting in the verification of patient eligibility
Development of data collection instruments and assistance with regulatory activities
Data entry
Assurance of conduct of protocol in accordance with applicable NCI and FDA guidelines
Maintenance of study patient records and source documentation
Coordinating orders, scheduling and study drug administration with the clinical team
Supporting clinical care team with completion of research‑required tests and assessments
Acting as liaison between research protocol and clinic staff, pharmacy, and research participants
Ensuring that patient billing is accurate and assisting manager and financial team in verifying appropriate clinical‑trial billing; participation in patient consenting
Support and periodic coverage to and across study teams, as delegated by the Clinical Research Manager, including maintaining regulatory documents, patient visits and study assessments (e.g., ECGs, vitals, specimen collection, management and shipping, requesting medical records, and other study‑related tasks as needed)
This TI Clinical Research Assistant will have direct patient contact, process biological samples, and may perform other non‑invasive testing such as ECGs. The assistant will also assist in the continuing education of physicians, residents, interns, nurses and other related personnel regarding knowledge of clinical trials and activities.
Required Qualifications
Bachelor’s Degree in a relevant field and 1 year of relevant experience
Associate’s Degree and 3 years of relevant experience
No degree and 4 years of relevant experience
Equivalent combination of training and experience
Required Competencies
High degree of attention to detail
Ability to prioritize and complete multiple tasks simultaneously
Excellent communication, analytical and organizational skills (written and verbal)
Ability to work independently and as part of a team while collaborating to resolve problems
Proficiency with Windows PC applications (e.g., MS Excel, Oracle, Access, Word, PowerPoint)
Demonstrated excellent customer‑service skills both on the phone and in person
Energy and drive to coordinate multiple projects simultaneously
Use of tact and diplomacy to maintain effective working relationships
Critical thinking skills
Time‑management skills
Guiding Principles
We act BOLDLY—Breakthroughs require pushing the boundaries of science, exploring new frontiers, and thinking differently.
We SUPPORT each other—Respect leads to trust, which leads to excellence.
We work as a CONNECTED team—We must leverage our collective brain power to conquer cancer because no one individual can do it alone.
Preferred Qualifications
Clinical trial knowledge with a minimum of 1 year of research experience
Experience conducting different phases of projects, including data collection and 3-5 years of clinical trial experience
Networking and database systems proficiency
Medical terminology knowledge
Working knowledge of EPIC
CCRP or ACRP certification
Typing speed 40+ wpm
Additional Details
Apply online. Please be sure to include a resume or CV and cover letter with your application.
Equal Employment Opportunity
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
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Worksite address
portland, OR, 97204, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.