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Clinical Research Associate Jobs in Springfield, OR

Team RN

Springfield, OR · On-site

$42 - $69.46/hr

Support clinical research activities and act as a resource for LPNs and medical assistants. * If ... Associate's degree in nursing from an accredited program for professional nursing education; BSN ...

Team RN

Springfield, OR · On-site

$42 - $69.46/hr

Support clinical research activities and act as a resource for LPNs and medical assistants. * If ... Associate's degree in nursing from an accredited program for professional nursing education; BSN ...

Radiation RN

Eugene, OR · On-site

$42 - $69.46/hr

Other duties as assigned. * Assist and collaborate with clinical research. * Participates in ... Associates in Nursing degree from an accredited program for professional nursing education; BSN ...

Radiation RN

Eugene, OR

$42 - $69.46/hr

Other duties as assigned. * Assist and collaborate with clinical research. * Participates in ... Associates in Nursing degree from an accredited program for professional nursing education; BSN ...

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Clinical Research Associate information

See Springfield, OR salary details

$12

$42

$72

How much do clinical research associate jobs pay per hour?

As of Aug 23, 2026, the average hourly pay for clinical research associate in Springfield, OR is $42.57, according to ZipRecruiter salary data. Most workers in this role earn between $29.86 and $54.47 per hour, depending on experience, location, and employer.

What is a clinical research associate?

Clinical Research Associates (CRAs) are professionals responsible for monitoring and overseeing clinical trials to ensure they are conducted in accordance with regulatory guidelines, protocols, and ethical standards. They play a key role in ensuring the safety of trial participants and the integrity of collected data. CRAs often visit clinical trial sites to verify data accuracy, maintain study documentation, and provide training to site staff. Their work ensures that new drugs, treatments, or medical devices are tested rigorously before they reach the market.

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

To thrive as a Clinical Research Associate, you need a solid background in life sciences, attention to detail, and experience with clinical trial protocols, often supported by a relevant bachelor's degree. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) guidelines, and sometimes certifications like ACRP or SOCRA is typically required. Strong organizational, communication, and problem-solving skills help build effective relationships with research sites and ensure compliance. These skills are vital for maintaining the integrity of clinical trials, ensuring regulatory adherence, and advancing medical research efficiently.

What are some common challenges clinical research associates face when monitoring clinical trial sites?

Clinical Research Associates (CRAs) often encounter challenges such as ensuring protocol compliance across multiple sites, managing tight project timelines, and maintaining accurate documentation. Additionally, CRAs must effectively communicate with site staff to resolve issues and ensure data integrity, all while adhering to regulatory guidelines. Balancing frequent travel, adapting to different site environments, and handling unexpected issues such as patient recruitment delays are also typical aspects of the role.

What is the difference between Clinical Research Associate vs Clinical Trial Coordinator?

AspectClinical Research AssociateClinical Trial Coordinator
CredentialsBachelor's degree, often with clinical research certificationsBachelor's degree, often with clinical research or healthcare certifications
Work EnvironmentMonitors clinical sites, reviews data, ensures complianceCoordinates trial activities, manages schedules, and communicates with sites
Employer & IndustryPharmaceutical companies, CROs, biotech firmsHospitals, research institutions, CROs

Both roles are essential in clinical trials, with CRAs focusing on site monitoring and compliance, while Clinical Trial Coordinators handle day-to-day trial management. They often collaborate but have distinct responsibilities within the clinical research process.

Is being a clinical research associate worth it?

A clinical research associate (CRA) monitors clinical trials to ensure compliance with protocols and regulations, often requiring strong organizational and communication skills. The role offers opportunities for career growth, competitive salaries, and work in the healthcare or pharmaceutical industries, but it can involve irregular hours and travel. Overall, it can be a rewarding career for those interested in medical research and patient safety.

Is it hard to get a clinical research associate job?

Securing a clinical research associate (CRA) position can be competitive, often requiring a relevant degree in life sciences or healthcare, along with experience in clinical trials. Strong organizational skills, knowledge of Good Clinical Practice (GCP), and familiarity with trial management tools can improve job prospects, but entry-level roles may be easier to obtain with relevant internships or certifications.
More about Clinical Research Associate jobs

What are the most commonly searched types of Clinical Research jobs in Springfield, OR?

The most popular types of Clinical Research jobs in Springfield, OR are:

What job categories do people searching Clinical Research Associate jobs in Springfield, OR look for?

The top searched job categories for Clinical Research Associate jobs in Springfield, OR are:

What cities near Springfield, OR are hiring for Clinical Research Associate jobs?

Cities near Springfield, OR with the most Clinical Research Associate job openings:

Infographic showing various Clinical Research Associate job openings in Springfield, OR as of August 2026, with employment types broken down into 1% As Needed, 74% Full Time, 23% Part Time, 1% Temporary, and 1% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $88,539 per year, or $42.6 per hour.

RN - Clinical Research Coordinator

The US Oncology Network

Eugene, OR

$27.68 - $70/hr

Full-time

Life, Retirement

Posted 3 days ago

New


US Oncology rating

7.1

Company rating: 7.1 out of 10

Based on 109 frontline employees who took The Breakroom Quiz

382nd of 893 rated healthcare providers


Job description

Overview

RN - Clinical Research Coordinator

 

The Willamette Valley Cancer Institute and Research Center is actively seeking an RN - Clinical Research Coordinator for our location in Eugene, Oregon. WVCI, which is part of The US Oncology Network, provides their patients with start of the art clinical trials to help patients on their journey through the cancer care continuum. This individual would be working directly with the patients taking part in the studies, coordinating with medical and research team involved. While clinical research experience is preferred, an individual with a passion for all things clinical and analytical will find success in this role. This role will also support and adhere to the US Oncology Compliance Program, to include the Code of Ethics and Business Standards.

 

The general pay scale for this position at WVCI is $27.68 - $70.00. The actual hiring rate is dependent on many factors, including but not limited to: prior work experience, education, job/position responsibilities, location, work performance, internal equity, etc.

 

Employment Type: Full time, 40 hrs (1.0 FTE)

Benefits: M/D/V, Life Ins., 401(k)

Location: Eugene, OR


Responsibilities
  • Screens potential patients for protocol eligibility.
  • Presents trial concepts and details to the patients, participates in the informed consent process, and enrolls patients on protocol.
  • Coordinates patient care in compliance with protocol requirements.
  • May disburse investigational drug and provide patient teaching regarding administration.
  • Maintains investigational drug accountability.
  • In collaboration with the physician, reviews patients for changes in condition, adverse events, concomitant medication use, protocol compliance, response to study drug and thoroughly documents all findings.
  • Responsible for accurate and timely data collection, documentation, entry, and reporting.
  • Schedules and participates in monitoring and auditing activities.
  • Maintains regulatory documents in accordance with USOR SOP and applicable regulations.
  • Participates in required training and education programs.
  • Responsible for education of clinic staff regarding clinical research.
  • May collaborate with Research Site Leader in the study selection process.
  • Additional responsibilities may include working directly with other (non-USOR) research bases and/or sponsors.
  • Provides a safe environment for patients, families, and clinical staff at all time through compliance with all federal, state, and professional regulatory standards as issued through OSHA and the CDC. Maintains strict patient confidentiality according to HIPAA regulations and applicable law.
  • Other duties as assigned

Qualifications
  • Associate's degree in a clinical or scientific related discipline desired, Bachelor's degree preferred.
  • RN License in OR REQUIRED
  • Minimum two to three (2-3) year of experience in a clinical or scientific related discipline, preferably in oncology.
  • Oncology research experience preferred.
  • EMR experience preferred. 
  • SoCRA or ACRP certification preferred.

Physical Demands:

The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Requires full range of body motion including handling and lifting patients, manual and finger dexterity, and eye-hand coordination. Requires standing and walking for extensive periods of time. Occasionally lifts and carries items weighing up to 40 lbs. Requires corrected vision and hearing to normal range.

Working Conditions:

The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Exposure to communicable diseases, toxic substances, ionizing radiation, medical preparations and other conditions common to an oncology/hematology clinic environment.

The US Oncology Network is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, or national origin.

Qualifications:
  • Associate's degree in a clinical or scientific related discipline desired, Bachelor's degree preferred.
  • RN License in OR REQUIRED
  • Minimum two to three (2-3) year of experience in a clinical or scientific related discipline, preferably in oncology.
  • Oncology research experience preferred.
  • EMR experience preferred. 
  • SoCRA or ACRP certification preferred.

Physical Demands:

The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Requires full range of body motion including handling and lifting patients, manual and finger dexterity, and eye-hand coordination. Requires standing and walking for extensive periods of time. Occasionally lifts and carries items weighing up to 40 lbs. Requires corrected vision and hearing to normal range.

Working Conditions:

The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Exposure to communicable diseases, toxic substances, ionizing radiation, medical preparations and other conditions common to an oncology/hematology clinic environment.

The US Oncology Network is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, or national origin.

Education:UNAVAILABLEEmployment Type: FULL_TIME

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