Oregon Health & Science University

Clinical Research Associate

Job Locations US-OR-Portland
Requisition ID
2025-34216
Position Category
Research
Position Type
Regular Full-Time
Job Type
Research
Department
Population Science - Knight Cancer Institute
Salary Range
Range minimum is $57,928/year. Your yearly rate will be determined based on education, experience, and internal equity
FTE
1.00
Schedule
Monday - Friday; occasional nights and weekends
Hours
8:30am-5:00pm
HR Mission
School of Medicine
Drug Testable
No

Department Overview

The OHSU Knight Cancer Institute, known as one of the pioneers in personalized cancer medicine, is an international leader in research and cancer treatment. Driven by its mission to end cancer as we know it, the institute is building upon its expertise in targeted treatments to advance the early detection of cancer when the disease is most treatable.

 

 

Every Knight Cancer employee is expected to embody our 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

Function/Duties of Position

We are seeking a full-time Clinical Research Associate to serve as Project Director (PD) of a clinical research study in people with cancer, specifically cancer survivorship, treatment-related toxicities and rehabilitation strategies. The PD will work directly with the PI, Lab Manager, and Intervention Supervisor to execute all aspects of the clinical research, with particular oversight for recruitment and data collection. This person is responsible for day-to-day project management duties and will be responsible for overseeing elements of the project that may include: participant recruitment and retention, development of study recruitment materials and procedures, regulatory compliance, data quality and management, intervention delivery, budget management, progress reporting and dissemination. Day-to-day research responsibilities include overseeing research assistants/student trainees on scheduling of participants for appointments, overseeing collection, entry and quality of data, communicating with study participants as needed, purchasing research supplies, and working in partnership with the members of the study team to maintain scientific quality across all studies. They will also be writing data summaries, project reports, and possibly presenting research findings at scientific meetings. We expect the Clinical Research Associate to work with the team to identify and resolve research issues, develop research ideas, and disseminate results. The ideal candidate is ambitious and eager to contribute to the PI’s program of research, has strong communication skills both within a team environment and with participants, has strong organizational skills, and can demonstrate a commitment to maintaining the integrity and quality of data collection in a research environment. Must be able to work and lead independently, including maintaining oversight of study timelines, benchmarks, milestones, and deliverables. A positive, solution-oriented mindset is required! The person hired must be CPR/First Aid certified or be willing to obtain this prior to the position's start date. This is a grant funded position for up to one year but may be extended depending on project needs and funding.

 

Oversee study timelines and benchmarks: Oversee and manage research grants and maintain oversight and delegation of study timelines, benchmarks, milestones, and deliverables. Organize and run investigator meetings. Coordinate activities between research sites

 

Oversee recruitment: develop and maintain recruiting strategies, lead recruiting functions, accrue near/at target sample for studies

 

Maintain regulatory documents / compliance: maintain all IRB and related documentation, submit modifications and annual reports; assure all internal regulatory documentation are obtained, stored and secured according to protocol; assure compliance with all regulatory policies and procedures

 

Oversee data collection systems and activities: strive for high compliance and retention in the study, maintain study data bases, perform regular data checks, clean data in preparation for statistical analysis

 

Assist with data analysis, abstract/manuscript preparation and progress reports: conduct simple descriptive data analysis; work with statistical team on analysis planning and execution; contribute to manuscript preparation through construction of tables, figures and text; prepare annual progress reports for sponsor

 

Oversee research assistant team: Train and supervise Research Assistants in participant recruitment and data management, including data quality control, preliminary analysis and reports.

Required Qualifications

Education & experience:

  • Master's Degree in relevant field AND 3 years of clinical research coordination experience OR
  • Bachelor's Degree in relevant field AND 5 years of clinical research Coordination experience
  • 3 years of relevant experience

Knowledge, skills, and abilities:

  • Ability to attend to details and complete assignments with minimal direction 
  • Prior experience in human research studies (recruitment, data collection)
  • Ability to work with PI and lab manager and other project directors to independently carry out research and related work 
  • Ability to communicate clearly and consistently, demonstrate a high level of professionalism and interact well with collaborators, participants, and medical staff
  • Proficiency in Microsoft (Office Word, Excel, Outlook, and other MS office programs)
  • Excellent verbal and written communication skills in English language
  • First Aid/CPR Certified

Preferred Qualifications

  • Master’s Degree or higher in exercise science, health promotion, nutrition, health education, nursing or related field required
  • Prior experience conducting clinical research at OHSU.
  • Experience recruiting participants in a clinic setting.
  • Experience/familiarity with clinical assessments including physical performance (mobility, balance, etc.).
  • Experience using EPIC, REDCap, and eIRB.

Additional Details

Apply online. Please be sure to upload a Cover Letter and Resume/CV.

Please include a cover letter and names and contact information for 3 professional references.

 

We offer a variety of benefits on top of joining a thriving organization:

  • Medical, dental and vision coverage at no or low cost to employees
    • Covered 100% for full-time employees and 88% for dependents
  • Several retirement plans to choose from with contributions from OHSU
  • 25 days a year of paid time off
  • 8 days of sick time off
  • Commuter subsidies
  • Tuition reimbursement
  • Access to group life insurance, disability insurance and other supplemental benefits
  • Annual Merit Increase
  • Growth/Development Opportunities
  • Employee discounts to local and major businesses

#linkedin #indeed #knightcancerjobs #knightresearchandlabjobs #knightclinicalresearchjobs 

All are welcome

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.

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