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Research Associate Jobs in Ridgefield, WA (NOW HIRING)

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Clinical Research Associate II

Portland, OR

$91K - $114K/yr

Clinical Research Associate - Oncology - West Region ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients ...

RD SOLUTIONS INC

Data Scanning Associate

Vancouver, WA · On-site

$16.75 - $21.75/hr

Research Associate Are you tired of being unsure how much your delivery/driver job will pay? Will the customer tip? We have a great side hustle job for you! Our jobs are preplanned with a flexible ...

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CRA II and Senior CRA

Portland, OR · Remote

$91K - $114K/yr

We are currently seeking a Clinical Research Associate (Level II or Senior) to join our diverse and dynamic team. As a CRA II/Senior CRA at ICON, you will play a pivotal role in designing and ...

RetailData

Data Scanning Associate

Vancouver, WA · On-site

$16.75 - $21.75/hr

As a Research Associate, you can enjoy the flexibility of choosing when and how much you earn. All you need is reliable transportation to start making money. Why scan with RDSolutions? Choose your ...

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All JobsResearch Associate JobsResearch Associate Jobs in Ridgefield, WA

Research Associate information

See Ridgefield, WA salary details

$17

$34

$49

How much do research associate jobs pay per hour?

As of Aug 9, 2026, the average hourly pay for research associate in Ridgefield, WA is $34.53, according to ZipRecruiter salary data. Most workers in this role earn between $27.79 and $39.28 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a research associate, and why are they important?

To thrive as a Research Associate, you need a strong background in research methodology, data analysis, and subject-specific knowledge, typically supported by a relevant bachelor's or master's degree. Familiarity with statistical software (such as SPSS, R, or Python), laboratory equipment, and research databases is often essential. Attention to detail, critical thinking, and clear written and verbal communication skills set outstanding Research Associates apart. These skills ensure accurate data collection, effective collaboration, and the production of reliable, impactful research outcomes.

What is a research associate?

Research Associates are professionals who support research projects in academic, scientific, or business settings. They assist with designing studies, collecting and analyzing data, and preparing reports or publications. Research Associates often work under the supervision of principal investigators or senior researchers, contributing their expertise to advance the goals of the project. Their responsibilities can vary depending on the field, but typically involve both administrative and hands-on research tasks.

How much does a research associate earn?

Research associates typically earn a median annual salary ranging from $40,000 to $60,000, depending on experience, education, and industry. Salaries can vary based on location, specialization, and the organization’s size, with some roles offering additional benefits such as research funding or professional development opportunities.

What does a research associate do?

As a research associate, you conduct research and analysis as directed by a senior researcher or project manager. Researchers work in a number of fields, including medical science, the social sciences, natural sciences, finance, management, and academia. Your specific duties and responsibilities differ depending on the field in which you work, but some features of your work are similar across industries. You typically do primary and secondary source research, organize and process data, analyze said data, and report on your findings to lead researchers or clinicians.

What are some typical challenges a research associate might face when managing multiple research projects simultaneously?

As a Research Associate, juggling multiple projects often requires strong organizational skills and the ability to prioritize tasks effectively. You might encounter challenges such as balancing deadlines, coordinating with various team members, and adapting to shifting project goals or data requirements. Effective communication and proactive time management are essential to ensure each project progresses smoothly and meets its milestones. Many teams use project management tools and regular check-ins to help mitigate these challenges and support collaboration.

What is the difference between Research Associate vs Research Scientist?

AspectResearch AssociateResearch Scientist
Required CredentialsBachelor's or Master's degree in relevant fieldMaster's or PhD in relevant field
Work EnvironmentLaboratories, research institutions, universitiesLaboratories, research institutions, industry settings
Employer & Industry UsageAcademic, government, non-profitAcademic, industry, biotech, pharma
Common Search & ComparisonYesYes

The main difference between a Research Associate and a Research Scientist lies in their educational requirements and level of experience. Research Associates typically hold a bachelor's or master's degree and assist in research projects, while Research Scientists usually have a PhD and lead research efforts. Both roles work in similar environments like labs and research institutions, but Research Scientists often have more independence and responsibility.

Is a research associate a good career?

A research associate role is a valuable entry-level position in academia, industry, or government, involving data collection, analysis, and reporting. It offers opportunities to develop research skills, collaborate with professionals, and advance to higher-level positions with experience and additional qualifications.
More about Research Associate jobs
What are the most commonly searched types of Research jobs in Ridgefield, WA? The most popular types of Research jobs in Ridgefield, WA are:
What cities near Ridgefield, WA are hiring for Research Associate jobs? Cities near Ridgefield, WA with the most Research Associate job openings:
Research Associate jobs near you
Infographic showing various Research Associate job openings in Ridgefield, WA as of August 2026, with employment types broken down into 1% As Needed, 69% Full Time, 27% Part Time, 1% Temporary, and 2% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $71,820 per year, or $34.5 per hour.

TI Clinical Research Associate

Oregon Health & Science University

Portland, OR • On-site

$60K - $101K/yr

Full-time

Re-posted 11 days ago

Oregon Health & Science University rating

8.1

Company rating: 8.1 out of 10

Based on 95 frontline employees who took The Breakroom Quiz

158th of 617 rated colleges and universities

Job description

Department Overview
The Department of Neurological Surgery in the OHSU School of Medicine is a safe, respectful, and welcoming place for people of all races, cultures, ethnicities, genders, national origins, abilities, ages, colors, religions, and sexual orientations. We are committed to learning, promoting inclusion, and working to abolish inequities in our workplace here at OHSU, in our region, in our nation, and in our world. The Department of Neurological Surgery promotes an equitable work environment with a strong commitment to diversity. All department members will actively participate in training and events that reinforce and expand on this commitment.
Function/Duties of Position
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.

Study Coordination- Responsible for coordinating many aspects of oncology clinical trials from startup to closeout and assuring conduct of trials in accordance with NCI and FDA guidelines. This includes but is not limited to:
  • Be able to navigate complex oncology clinical trial protocols that can be upwards of a 670 page document
  • Schedule any necessary site-initiation/training visits for clinical trial start-up.
  • Explain trial logistics to oncology patients, triage and ensure all patient questions are answered.
  • Assist the PI or Sub-I with the informed consent process
  • Assist the PI or Sub-I with the collection and documentation of subject adverse events
  • Document study required source documentation in the subjects eMR or paper source
  • Communicate with the PI or Sub-I during patient visits regarding dose modification parameters
  • Serve as the liaison between the study staff and the medical monitor for patient level protocol questions
  • Serve as the point of contact for the clinical staff to provide protocol guidance for patient management on trial
  • Serve as the liaison between subjects, physicians, and sponsors.
  • Assist CRA specialist or take lead in resolving clinic operations issues
  • Field research patient calls to the personnel most appropriately trained to address their questions/needs
  • Coordinate recruitment, scheduling, preparation and testing of research subjects
  • Place research lab and procedure orders
  • Review patient records to screen for potential trials
  • Problem solve barriers for patients to participate in clinical trials. This may include working with their PCP or local oncologist to get procedures done close to home, connecting them to social work to find travel and financial resources, setting up virtual medicine visits or referring to another useful resource.
  • Performing drug accountability with patients and documenting in the patients eMR or on paper source.
  • Prepping for upcoming visits including reviewing patient records to look for newly reported AEs, Conmeds and other pertinent information to be reviewed with the patient and provider at the visit
  • Submit insurance pre-authorization request for new patients on study
  • Schedule research biopsies, scans, ECHOs/ECGs, Ophthalmology appointments, dermatology visits and other research required procedures as needed.
  • Provide clinic training in-services as needed
  • Ship out central study labs as needed
  • Prepare and ship subject samples as needed by study.
  • Review patient data to determine appropriate eligibility and deficiencies regarding enrollment into clinical trials. Confirm with investigator that subject meets appropriate inclusion criteria for clinical trial.
  • Communicate all pre-treatment requirements to investigator/clinical staff.
  • Obtain and submit imaging studies, pathology, or other samples as required by protocol.
  • Review billing schedule and billing errors. Ensure appropriate patient billing and reimbursement.
  • Submit Invoices for tasks related to their role
  • Review and report adverse events or Unanticipated Problems to IRB/study sponsor.
  • Obtain vital sign measurements for study patients; documenting contacts with study subjects and vital signs as appropriate.
  • Procure and process human biological specimens (including but not limited to blood, urine, feces, sputum, tissue) in adherence with protocol parameters and appropriate training.
  • Communicate and facilitate oncology trial guidelines, timelines, and patient specifics with Research Pharmacy, Clinics and various service departments to coordinate treatment for study patient.
  • Perform or collaborate with research team member's to ensure that data entry and chart review/abstraction is completed to verify that key data has been reported to the clinical research database or reported to the sponsor in the required format.
  • Review follow up data clarifications or data queries and report within study timeline.
  • Maintain and update or collaborate with research team member's to ensure that subject data records are correct for study analysis and survival.
  • Assist investigators with any special requests for data retrieval and/or evaluation and analysis of clinical data for ongoing research studies.
  • Ensure compliance with FDA and regulatory reporting agencies, Health Insurance Portability and Accountability Act (HIPAA), and Good Clinical Practice (GCP) standards
  • Report any non-compliance to study investigator / departmental staff.
  • Prepare any necessary materials for required internal and external (sponsor, FDA) regulatory and quality control audits and sponsor monitoring visits.
  • Coordinate and schedule clinical trial monitoring visits
  • May assist and collaborate with principal investigator and sub-principal investigators in clinic during patient appointments, consenting appointments and treatment appointments to ensure protocol is being adhered to and proper documentation is recorded.

Disseminate Clinical Research Information to Program:
  • Navigate interdepartmental processes and relationships to ensure compliant study implementation.
  • In collaboration with Regulatory Team:
    • Distribute clinical research related information to appropriate research team / affiliated institutional personnel as applicable.
    • Notify research team and those individuals directly involved in in pertinent areas of clinical research of protocol amendments, revisions, activations, closures and announcements.
    • Keep local Principal Investigator up to date on key information as related to the clinical research. Schedule and maintain records on appropriate trainings/meetings as needed.

Institutional Review Board (IRB) Compliance:
  • Work with regulatory management team to adhere to regulations at OHSU for initial and continuing regulatory approval of clinical protocols such as annual re-approval/continuing review, amendment approval; and submission of reportable information.
  • May perform regulatory documentation or creation of documents, as needed. Documents may include consent forms, IRB forms, and any necessary IRB documentation.

Design and Analysis:
  • Assist Principal Investigators with the preparation of abstracts, grant
    applications and publications.
  • Work with investigators to design experimental methods and/or operationalize the plan of clinical research projects to achieve protocol objectives.
  • Communicate effectively across multiple clinical teams for clinical trial coordination.

Education:
  • Participate in continuing education activities within the research program and other areas to maintain current knowledge of oncology disease process, research regulatory requirements, and process improvements for clinical trials.
  • May assist with or lead training of junior team members.

Financial Responsibilities:
  • Ensure correct ordering of procedures in compliance with the approved billing schedule.
  • Verify that procedures/services are billed in accordance with the approved billing schedule.
  • Collaborate with study team on financial planning and budget negotiation, as appropriate.

Additional duties: Additional duties as assigned by Clinical Research Manager
Required Qualifications
  • 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
  • SoCRA or ACRP required within 12 months of hire
  • Ability to prioritize multiple tasks at one time
  • Excellent communication, analytical and organizational skills: both written and verbal
  • Ability to work independently and as part of a team, while being collaborative in resolving problems
  • Proficiency with computers running Windows and PC applications e.g. MS Excel, Word and PowerPoint.
  • Excellent customer service skills
  • Energy and drive to coordinate multiple projects simultaneously
  • Ability to use tact and diplomacy to maintain effective working relationships

Preferred Qualifications
  • Bachelor's degree with coursework in science or related field
  • At least three years of direct clinical research experience
  • Research experience with some knowledge of clinical trials
  • Experience coordinating different phases of projects, including data collection
  • Customer service experience
  • Microsoft Office, Access, and other networking and database systems
  • Medical terminology
  • OHSU systems Oracle and/or Epic
  • CCRP

Additional Details
Must be able to travel to all Knight worksite locations, including using the tram. Coordinator will work with human biological samples, including samples which may contain infectious disease. Coordinator will be expected to travel to conferences, new study meetings, and may travel for study monitoring at other sites. Position will require occassional weekend work and ability to focus in a busy cubicle environment with multiple
Why apply to OHSU?
We are Oregon's only public academic health center.
In addition to caring for patients, we lead groundbreaking research. We also train the next generation of health care professionals. As Portland's largest employer, we give you opportunities to learn and advance in a system of hospitals and clinics across Oregon and Southwest Washington.
All are welcome.
OHSU welcomes people of all ages, ethnicities, genders, national origins, religions and sexual orientations. We are striving to build an anti-racist, multicultural institution and encourage people with diverse backgrounds to apply.
To request reasonable accommodation, contact askhr@ohsu.edu

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About Oregon Health & Science University

Sourced by ZipRecruiter

Oregon Health & Science University (OHSU) is a distinguished institution under the industry of higher education and healthcare, specifically in the field of medical science. Based in Portland, Oregon, US, it maintains a reputation for promoting research, teaching, patient care, and outreach. Established in 1887, OHSU has continually sought to redefine the parameters of healthcare delivery and biomedical discovery through its expansive catalog of programs and initiatives. A galvanizing mission drives OHSU: to improve the health and quality of life for all Oregonians through excellence, innovation, and leadership in health care, education, and research.

Industry

Colleges, universities, and professional schools

Company size

10,000+ Employees

Headquarters location

Portland, OR, US

Year founded

1887

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