1

Clinical Research Assistant Jobs in Oregon (NOW HIRING)

Function/Duties of Position This OHSU Knight Cancer Institute TI Sr. Clinical Research Assistant (TI Sr. CRA) is responsible for the collection, entry, general management of oncology study data and ...

next page

Showing results 1-20

Clinical Research Assistant information

See Oregon salary details

$8

$24

$48

How much do clinical research assistant jobs pay per hour?

As of Sep 6, 2026, the average hourly pay for clinical research assistant in Oregon is $24.01, according to ZipRecruiter salary data. Most workers in this role earn between $18.32 and $27.45 per hour, depending on experience, location, and employer.

What is a clinical research assistant?

Clinical Research Assistants are professionals who support clinical research studies by performing a range of administrative and research-related tasks. They help collect and manage data, assist with patient recruitment, prepare study materials, and ensure compliance with research protocols and regulations. Their work is crucial in advancing medical knowledge and ensuring that clinical trials run smoothly and ethically. Clinical Research Assistants often work under the supervision of principal investigators or clinical research coordinators in hospitals, universities, or pharmaceutical companies.

What does a clinical research assistant do?

A clinical research assistant—or clinical research associate (CRA)—helps lead researchers during clinical trials for new drugs and medical devices. As a clinical research assistant, your responsibilities include preparing the laboratory, processing volunteers, taking biological samples or vital signs, and organizing data. You may also be required to set up and clean work areas. Your job is to assist the researchers in any way possible, helping them conduct sound, ethical, and scientifically accurate research.

What are the key skills and qualifications needed to thrive as a clinical research assistant?

To thrive as a Clinical Research Assistant, you need a bachelor’s degree in a life science or health-related field, attention to detail, and strong organizational skills. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and good clinical practice (GCP) certification are typically required. Excellent communication, teamwork, and problem-solving abilities help you excel in coordinating with research teams and participants. These skills ensure accurate data collection, regulatory compliance, and the smooth execution of clinical studies.

What are some common challenges clinical research assistants face when coordinating multiple studies simultaneously?

Clinical Research Assistants often manage several studies at once, which can lead to challenges in balancing competing deadlines, maintaining accurate documentation, and ensuring compliance with complex protocols. Effective time management and organizational skills are crucial to handle overlapping tasks such as scheduling patient visits, collecting data, and preparing regulatory submissions. Collaborating closely with principal investigators, coordinators, and other team members helps distribute the workload and maintain research quality. Developing strong communication habits and utilizing digital tracking tools can further streamline workflow and reduce errors.

What is the difference between Clinical Research Assistant vs Clinical Research Coordinator?

AspectClinical Research AssistantClinical Research Coordinator
CredentialsTypically requires a bachelor's degree in health sciences or related field; certifications like CCRP are a plusRequires a bachelor's degree; certifications such as CCRP or CCRC are common
Work EnvironmentAssists in data collection, patient scheduling, and administrative tasks in clinical trial settingsManages study protocols, patient recruitment, and regulatory compliance in clinical trial sites
Employer & IndustryHospitals, research institutions, pharmaceutical companiesHospitals, research centers, pharmaceutical companies

Both roles support clinical research but differ in responsibilities. Clinical Research Assistants focus on data collection and administrative tasks, while Clinical Research Coordinators oversee study management and patient interactions. Understanding these differences helps in choosing the right career path or job search focus.

Can you be a clinical research assistant with no experience?

Clinical research assistant positions often require some knowledge of medical terminology and data management, but many entry-level roles are available for candidates without prior experience. Employers may provide on-the-job training and look for strong organizational skills, attention to detail, and the ability to follow protocols. Certifications such as Good Clinical Practice (GCP) can enhance prospects for those new to the field.

What are the most commonly searched types of Clinical Research jobs in Oregon?

The most popular types of Clinical Research jobs in Oregon are:

What are popular job titles related to Clinical Research Assistant jobs in Oregon?

For Clinical Research Assistant jobs in Oregon, the most frequently searched job titles are:

What cities in Oregon are hiring for Clinical Research Assistant jobs?

Cities in Oregon with the most Clinical Research Assistant job openings:

Infographic showing various Clinical Research Assistant job openings in Oregon as of August 2026, with employment types broken down into 2% As Needed, 70% Full Time, 20% Part Time, 7% Contract, and 1% Nights. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $49,947 per year, or $24 per hour.

Clinical Research Assistant I

Portland VA Research Foundation

Portland, OR • On-site

$61.93/hr

Other

Posted 19 days ago


Job description

Job Title: Clinical Research Assistant I

Department: Research

Reports To: Mark Garzotto, MD

FLSA Status: Full Time, Non-exempt

Pay Rate: $21.63 - $24.04 per hour

Work Type: Onsite

POSITION SUMMARY

Clinical Research Assistants support the implementation of clinical trials by conducting study visits, preparing participant materials, collecting data, and helping ensure studies are well organized and in compliance with protocols. This role offers direct exposure to patient interactions, clinical workflows across multiple medical specialties, and regulatory processes. Research Assistants work closely with Study Coordinators, Principal Investigators, clinicians, and patients, gaining valuable experience that can serve as a strong foundation for advancement into Study/Project Coordinator roles and beyond. Responsibilities provide meaningful opportunities for hands‑on learning and professional development in both research and healthcare, while supporting Veterans and their caregivers.

We are seeking a dedicated Clinical Research Assistant to take primary responsibility for multiple aspects of human subjects research with Veteran patients. Our current research includes prostate, bladder, hematologic, gastrointestinal, and skin cancer clinical trials. This position involves direct patient interaction in a clinical setting with prospective and retrospective data collection.

This position is located in the Research and Development Service of the VA Portland Health Care System (VAPORHCS) in Portland, Oregon.

ESSENTIAL DUTIES AND RESPONSIBILITIES

  • Ensure the proper conduct of clinical trials according to protocol requirements
  • Recruit and communicate with Veteran participants in a clinical setting and by phone
  • Accurately screen, consent, and enroll eligible Veteran patients into clinical trials
  • Precisely and accurately document and organize source materials into patient records and electronic medical record systems (EMR)
  • Develop databases, participant tracking systems, and standard operating procedures for research projects
  • Accurately, thoroughly, and respectfully solicit health information from Veteran participants within a clinical setting and by phone
  • Ensure timely data collection, entry, auditing, and query resolution
  • Collect and ship research biospecimens
  • Manage Electronic Data Capture (EDC) across multiple trials and confirm participant timepoint completion
  • Work independently under general supervision of Principal Investigator and ensure tasks are completed accurately and on time.
  • Communicate any problems and concerns, and suggest solutions to the Program Manager, and/or appropriate Principal Investigator.

SUPERVISORY RESPONSIBILITY

This position has no direct reports.

QUALIFICATIONS

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

EDUCATION and EXPERIENCE

Required:

  • Bachelor's degree

Preferred:

  • Degree in science, social science, or other health related fields
  • Prior research experience, either volunteer, academic or professional

KNOWLEDGE, SKILLS, AND ABILITIES

Required:

  • English language proficiency with excellent oral and written communication skills
  • Must be able to count, calculate, interpret numerical data/graphs and perform basic mathematical calculations
  • Proficiency with Microsoft Office (Word, PowerPoint, Excel & Outlook)
  • Ability to communicate effectively and professionally via email, MS Teams Chat and other electronic platforms
  • Strong critical thinking and problem-solving skills as well as deductive and inductive reasoning abilities
  • Ability to independently meet deadlines, anticipate needs, prioritize multiple tasks, and follow through on tasks to completion
  • Excellent organizational skills with high attention to detail and accuracy
  • Ability to work independently, exhibit self-motivation and enthusiasm to learn new skills
  • Take initiative to identify and address issues and concerns of veteran patients in a timely and caring manner

Preferred:

  • Basic statistical, data interpretation and unit conversion knowledge
  • Prior experience using Electronic Data Capture (EDC) systems such as REDCap, Medidata, or Inform

ADDITIONAL INFORMATION

Because this position is based in a VA facility, the Research Assistant must secure a VA Without Compensation Appointment (WOC) prior to starting work, and must maintain a WOC Appointment in order to continue employment.

The VA's WOC process will be facilitated by the supervisor and processed through the VA Research and Development office. The screening process required to obtain a WOC may include a background check, a credit check, a physical, a drug test, and a TB test.

After the WOC process has been completed, the VA also requires several trainings prior to employees starting work.

Portland VA Research Foundation is an equal opportunity and affirmative action employer. All qualified applicants will receive consideration for employment without regard to status as a protected veteran or a qualified individual with a disability, or other protected status such as race, color, sex, sexual orientation, gender identity, religion, national origin or age.

All PVARF employees are required to be fully vaccinated for COVID-19 within 8 weeks of hire, unless medically exempt. Employees will be required to provide either proof of vaccination or an approved medical exemption prior to beginning work.

#J-18808-Ljbffr