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Clinical Study Associate Jobs in Oregon (NOW HIRING)

Natera

Senior Clinical Research Associate

OR · On-site +1

The Senior Clinical Research Associate is responsible for the overall operational execution of ... Develop study-related documents with minimal Clinical Trial Manager guidance including: protocol ...

Natera

OR · On-site

POSITION SUMMARY: We are seeking an Associate Director, Clinical Science to architect trial ... Design robust clinical study concepts, specifying overall design parameters, sample-size logic ...

Syneoshealth

Clinical Research Associate - Full-Service

OR · On-site +1

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

May act as primary liaison with study site personnel, or in collaboration with Central Monitoring Associate. Ensures all assigned sites and project-specific site team members are trained and ...

Abbott

Clinical Associate

Portland, OR · On-site

  • Medical

  • Retirement

As a Clinical Associate on the U.S. Abbott EP team, you will provide clinical and technical support ... Participating in clinical studies/data collection; * Troubleshooting; and, * Leading/supporting new ...

Abbott

Clinical Associate

Portland, OR · On-site

  • Medical

  • Retirement

As a Clinical Associate on the U.S. Abbott EP team, you will provide clinical and technical support ... Participating in clinical studies/data collection; * Troubleshooting; and, * Leading/supporting new ...

Abbott

Clinical Associate

Portland, OR · On-site

  • Medical

  • Retirement

As a Clinical Associate on the U.S. Abbott EP team, you will provide clinical and technical support ... Participating in clinical studies/data collection; * Troubleshooting; and, * Leading/supporting new ...

Spyre Therapeutics

Associate Director, Medical Writing

OR · On-site +1

$170K - $199K/yr

  • Medical

  • Retirement

  • PTO

As Associate Director, Medical Writer, you will lead or make key contributions to clinical and ... clinical and regulatory documents, including but not limited to clinical study protocols ...

Icon plc

CRA II and Senior CRA

Portland, OR · Remote

$91K - $114K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

... in a study coordinator or nursing role. * Minimum of 1 year independent monitoring to be considered for a Clinical Research Associate II and a minimum of 3 years independent monitoring to be ...

410 ICR United States USA

CRA II and Senior CRA

Portland, OR · Remote

$91K - $114K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

... in a study coordinator or nursing role. * Minimum of 1 year independent monitoring to be considered for a Clinical Research Associate II and a minimum of 3 years independent monitoring to be ...

Travere

Associate Director, Medical Writing

OR · On-site +1

Position Summary: The Associate Director, Medical Writing is responsible for oversight and ... clinical study reports (CSRs), Investigator's Brochures (IBs), and Periodic Safety Update Reports ...

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Clinical Study Associate information

See Oregon salary details

$13

$33

$58

How much do clinical study associate jobs pay per hour?

As of Aug 18, 2026, the average hourly pay for clinical study associate in Oregon is $33.35, according to ZipRecruiter salary data. Most workers in this role earn between $22.36 and $43.99 per hour, depending on experience, location, and employer.

What is a clinical study associate?

Clinical Study Associates (CSAs) are professionals who support the planning, execution, and monitoring of clinical trials in the pharmaceutical, biotechnology, or medical device industries. They help coordinate study logistics, maintain study documentation, and ensure compliance with regulatory requirements. CSAs often work closely with Clinical Research Associates, study coordinators, and investigators to ensure that trials are conducted according to protocol and timelines. Their role is essential in ensuring the accuracy and integrity of data collected during clinical research.

What are some common challenges clinical study associates face when managing multiple clinical trials simultaneously?

Clinical Study Associates often juggle several clinical trials at once, which can present challenges such as prioritizing competing deadlines, maintaining accurate documentation for each study, and ensuring consistent communication with cross-functional teams. Staying organized and proactive is essential, as unforeseen protocol amendments or site issues can arise. Building strong relationships with site staff and utilizing effective project management tools can help CSAs navigate these complexities and deliver high-quality results.

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

To thrive as a Clinical Study Associate, you need a strong understanding of clinical research processes, regulatory requirements, and typically a life sciences degree. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and GCP certification are commonly required. Attention to detail, organizational skills, and effective communication set top performers apart in this role. These competencies ensure accurate study documentation, regulatory compliance, and smooth coordination across research teams.

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

AspectClinical Study AssociateClinical Research Coordinator
CredentialsBachelor's degree, often in life sciences; certifications like CCRP or CCRA beneficialBachelor's degree in health sciences or related field; certifications like CCRP advantageous
Work EnvironmentPharmaceutical companies, CROs, clinical trial sitesHospitals, clinics, research centers
Job FocusMonitoring clinical trials, ensuring protocol compliance, data accuracyManaging daily trial activities, patient recruitment, data collection
Employer & Industry UsageCommonly employed in pharma and CROsPrimarily in healthcare and academic research settings

Both roles involve clinical trial oversight but differ in focus: Clinical Study Associates primarily monitor and ensure compliance during trials, while Clinical Research Coordinators manage daily trial operations and patient interactions. Understanding these distinctions helps in choosing the right career path or job search focus.

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

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

What cities in Oregon are hiring for Clinical Study Associate jobs?

Cities in Oregon with the most Clinical Study Associate job openings:

Clinical Study Associate jobs near you
Infographic showing various Clinical Study Associate job openings in Oregon as of August 2026, with employment types broken down into 1% As Needed, 68% Full Time, 29% Part Time, 1% Temporary, and 1% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $69,362 per year, or $33.3 per hour.

Senior Clinical Research Associate

Natera

OR • On-site, Remote

Full-time

Posted 19 days ago

Natera rating

7.7

Company rating: 7.7 out of 10

Based on 38 frontline employees who took The Breakroom Quiz

56th of 120 rated laboratories

Job description

POSITION SUMMARY:

The Senior Clinical Research Associate is responsible for the overall operational execution of clinical studies on one or more clinical projects/programs; from study concept through study completion. This position will perform required job duties with guidance from Clinical Trial Managers to ensure that trial timelines, costs, and quality metrics are met, and the study is conducted in compliance with the study protocol, SOPs, and applicable regulatory requirements helps design and execute clinical research activities.

PRIMARY RESPONSIBILITIES:

  • Provide high level logistical support for clinical study operations, including study start up, study supplies, site qualification, site initiation, site management, study monitoring, and close out for clinical research studies and collaborations

  • Develop study-related documents with minimal Clinical Trial Manager guidance including: protocol, informed consent forms, training materials, protocol amendments, monitoring plans, synopses, and ethics committee submissions, as required

  • Manage small to medium size study contracting, budget, invoicing and payment process for all clinical trial vendors including investigative sites with minimal oversight

  • Support the Clinical Data Management team in the design and content of case report forms, completion guidelines, including support and testing of an EDC

  • Manage the preparation, handling, filing, and archiving of clinical documentation and reports according to SOPs and study requirements

  • Overseeing clinical trial supplies related to biospecimen collection, processing, shipment, and storage as, well as maintenance of associated tracking information  

  • Train CROs, vendors, investigators, and study coordinators on study requirements and provide guidance on site issues

  • Monitor and track clinical trial progress, provide status updates to stakeholders

  • Develop new study monitoring plans, and monitor studies following study monitoring plans to identify protocol deviations or data discrepancies

  • Perform study activities including consent participants for research studies, ethics board submissions, participant data and sample tracking using in-house and CRO databases, for studies where Natera functions as a Clinical Research Site.

  • Update Clinical Department SOPs with guidance from CTM and/or Director

  • Partner with other research and development groups at Natera to achieve deliverables

  • Perform other duties as assigned

  • This role works with PHI on a regular basis both in paper and electronic form and have an access to various technologies to access PHI (paper and electronic) in order to perform the job. 

  • Employee must provide records of current training or complete training relating to HIPAA/PHI privacy, Human Subjects Protection, and GCP.  

  • Must maintain a current status on Natera training requirements including General Policies, Procedure Compliance, and security training

  • Employee must pass post offer criminal background check    

QUALIFICATIONS:

  • BA/BS degree in life sciences, related field, or equivalent

  • Minimum of 4 years of experience working on clinical studies in the academic, biopharma, diagnostics, or medical device fields  

KNOWLEDGE, SKILLS AND ABILITIES:

  • Experience with clinical EDC systems,

  • Familiarity with the organization and structure of the Trial Master File (TMF)

  • Familiarity with bio sample management, sample processing, and biobanking best practices

  • Competency in SOPs, ICH-GCP, FDA Regulations

  • Proficiency in MS Word, Excel and PowerPoint

  • Demonstrated ability to work independently and lead projects

  • Demonstrated analytical skills and ability to identify complicated problems and propose solutions

  • Strong interpersonal skills and communication skills (both written and oral)

  • Excellent writing skills

  • Detail oriented, with solid organization and time management skills

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