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Research Coordinator Jobs in Remote, OR (NOW HIRING)

Deputy County Surveyor

Roseburg, OR ยท On-site

$71K - $94K/yr

... research survey records and evaluate aerial photographs; locate and document corners. Set horizontal and vertical control monuments; establish State plane coordinates and elevations. Lead and ...

Deputy County Surveyor

Roseburg, OR ยท On-site

$71K - $94K/yr

... research survey records and evaluate aerial photographs; locate and document corners. * Set horizontal and vertical control monuments; establish State plane coordinates and elevations. * Lead and ...

OSS-SIRT Engineer, Akrites

OR ยท On-site

$140K - $155K/yr

Defend Critical Open Source Software Against AI-Enabled Cyber Threats Akrites is a coordinated ... researcher communications * Support CVE/ID requests and aliasing workflows * Help maintain ...

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Showing results 1-20

Research Coordinator information

See Remote, OR salary details

$21.5K

$80.5K

$112.4K

How much do research coordinator jobs pay per year?

As of Sep 6, 2026, the average yearly pay for research coordinator in Remote, OR is $80,490.00, according to ZipRecruiter salary data. Most workers in this role earn between $60,900.00 and $99,400.00 per year, depending on experience, location, and employer.

What is a research coordinator?

A research coordinator supervises the daily activities of a study and monitors the activities of the subjects and researchers. As a research coordinator, your duties revolve around making sure that the study is conducted ethically and does not violate the research guidelines of the governing board or other agency. In short, you are responsible for making sure the study has as few flaws in its methodology as possible. You are also in charge of most administrative tasks. In this role, you can work on medical, technological, psychological, or other types of research projects, but you may work on clinical research most often.

What skills should I have to be a successful clinical research coordinator?

To thrive as a Research Coordinator, you need strong organizational abilities, attention to detail, and a relevant bachelor's degree or higher in a scientific or health-related field. Familiarity with research compliance systems, data management tools, and Institutional Review Board (IRB) protocols is commonly required. Excellent communication, problem-solving, and multitasking skills help you manage studies and collaborate effectively with diverse teams. These skills ensure the smooth execution of research projects, regulatory compliance, and the reliability of study outcomes.

What are some common challenges research coordinators face when managing multiple studies simultaneously?

Research Coordinators often juggle several studies at once, which can present challenges such as balancing competing deadlines, ensuring compliance with regulatory requirements, and managing communication among diverse stakeholders. Staying organized with detailed documentation and proactive scheduling is essential to prevent protocol deviations. Effective collaboration with principal investigators, sponsors, and clinical staff also helps to navigate unexpected changes and maintain study integrity.

What is the difference between Research Coordinator vs Research Assistant?

AspectResearch CoordinatorResearch Assistant
Required CredentialsBachelor's degree often required; some roles prefer or require a master'sTypically an undergraduate student or recent graduate; some roles may require a bachelor's degree
Work EnvironmentLeads study activities, manages protocols, interacts with stakeholdersSupports data collection, literature review, and administrative tasks
Employer & Industry UsageUsed in clinical, academic, and industry research settingsCommonly found in academic labs and research projects

The Research Coordinator generally has more responsibilities, including managing study protocols and liaising with stakeholders, while the Research Assistant provides support with data collection and administrative tasks. Both roles are essential in research projects but differ in scope and level of responsibility.

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

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

What are popular job titles related to Research Coordinator jobs in Remote, OR?

For Research Coordinator jobs in Remote, OR, the most frequently searched job titles are:

What job categories do people searching Research Coordinator jobs in Remote, OR look for?

The top searched job categories for Research Coordinator jobs in Remote, OR are:

What cities near Remote, OR are hiring for Research Coordinator jobs?

Cities near Remote, OR with the most Research Coordinator job openings:

Infographic showing various Research Coordinator job openings in Remote, OR as of August 2026, with employment types broken down into 1% As Needed, 88% Full Time, 10% Part Time, and 1% Contract. Highlights an 64% Physical, 3% Hybrid, and 33% Remote job distribution, with an average salary of $80,490 per year, or $38.7 per hour.

Senior Clinical Research Associate

Nexpro Technologies Inc

OR โ€ข Remote

$90K - $120K/yr

Full-time

Medical

Re-posted 28 days ago


Job description

We are seeking a detail-oriented and motivated Clinical Research Associate (CRA) to oversee and monitor clinical trials while ensuring compliance with study protocols, Good Clinical Practice (GCP), and regulatory requirements. The ideal candidate will have experience in site monitoring, clinical trial management, and maintaining high-quality clinical data.

Key Responsibilities

  • Monitor clinical trial sites to ensure compliance with study protocols, ICH-GCP, SOPs, and applicable regulatory guidelines.
  • Conduct Site Initiation Visits (SIV), Site Monitoring Visits (SMV), and Close-Out Visits (COV).
  • Verify source data and ensure data accuracy, integrity, and completeness.
  • Maintain Trial Master File (TMF) and essential study documentation.
  • Build and maintain strong relationships with investigators and site staff.
  • Identify, document, and resolve protocol deviations and study-related issues.
  • Ensure timely reporting of adverse events (AEs) and serious adverse events (SAEs).
  • Review informed consent documentation and ensure participant safety.
  • Prepare monitoring visit reports and follow-up letters.
  • Coordinate with Clinical Operations, Data Management, Biostatistics, Medical Writing, and Regulatory teams.
  • Support study start-up, patient recruitment, and site management activities.
  • Ensure studies are completed within timelines and quality standards.

Required Qualifications

  • Bachelor's or Master's degree in Life Sciences, Pharmacy, Nursing, Biotechnology, or a related field.
  • 2–6 years of experience as a Clinical Research Associate in clinical trials.
  • Strong knowledge of ICH-GCP, FDA, EMA, and local regulatory requirements.
  • Experience with EDC systems, CTMS, and eTMF platforms.
  • Excellent communication, documentation, and organizational skills.
  • Willingness to travel for site monitoring visits.

Preferred Skills

  • Clinical site monitoring experience across multiple therapeutic areas.
  • Knowledge of protocol review, source document verification (SDV), and risk-based monitoring.
  • Strong analytical and problem-solving abilities.
  • Ability to manage multiple studies simultaneously and work independently.

Benefits

  • Competitive salary and performance incentives.
  • Health insurance and employee wellness programs.
  • Learning and career development opportunities.
  • Collaborative and supportive work environment.

Company Description

NexPro Technologies offers robust, responsive and value-driven IT consulting and placement services.