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Remote Clinical Research Jobs in Remote, OR (NOW HIRING)

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Remote Duties : This position is responsible for Supporting the Project Management of RTSM ... Research Organization is required * Demonstrated knowledge of clinical development processes ...

New

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Remote Duties : This position is responsible for Supporting the Project Management of RTSM ... Research Organization is required * Demonstrated knowledge of clinical development processes ...

New

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Serve as a coding subject matter expert by analyzing clinical documentation, identifying ... Research new surgical procedures and emerging technologies to support accurate coding practices

Research Fellow, Pharma Toxicology

OR · On-site +1

$150K - $200K/yr

Ensure that nonclinical development plans and their execution align with overall product ... US - Remote All qualified applicants will receive consideration for employment without regard to ...

Partnering with Clinical Operations, Medical Affairs, Marketing, and Commercial teams, as well as ... Remote position * Ability to travel up to 40% of the time Servier's Commitment Servier is committed ...

... deliver clinical value. We use our proven track record as an innovator, our in-depth medical ... Remote: US What You'll Do: * Scaled and resilient security operations capabilities aligned with ...

... deliver clinical value. We use our proven track record as an innovator, our in-depth medical ... Remote: US What You'll Do: * Scaled and resilient security operations capabilities aligned with ...

... deliver clinical value. We use our proven track record as an innovator, our in-depth medical ... Location: * Remote - US / Canada What You'll Do: Cloud Operations & Reliability * Own the ...

... deliver clinical value. We use our proven track record as an innovator, our in-depth medical ... Location: * Remote - US / Canada What You'll Do: Cloud Operations & Reliability * Own the ...

... deliver clinical value. We use our proven track record as an innovator, our in-depth medical ... Remote: United States / Canada What You'll Do: * Own and drive the definition of all service ...

... deliver clinical value. We use our proven track record as an innovator, our in-depth medical ... Remote: United States / Canada What You'll Do: * Own and drive the definition of all service ...

We are global collaborators who achieve together-researching, manufacturing, and delivering ever ... In this vital role you will ensure all statistical aspects pertaining to clinical activities meet ...

Remote Clinical Research information

See Remote, OR salary details

$49K

$107.2K

$188.8K

How much do remote clinical research jobs pay per year?

As of Jul 29, 2026, the average yearly pay for remote clinical research in Remote, OR is $107,230.00, according to ZipRecruiter salary data. Most workers in this role earn between $80,900.00 and $122,400.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in the Remote Clinical Research position, and why are they important?

To thrive in Remote Clinical Research, a strong background in life sciences, research methodologies, and clinical trial protocols is essential, often supported by a relevant bachelor’s or master’s degree. Familiarity with tools such as Electronic Data Capture (EDC) systems, CTMS (Clinical Trial Management Systems), and certifications like Good Clinical Practice (GCP) are highly valued. Exceptional written and verbal communication, self-motivation, and organizational skills help remote researchers successfully collaborate and manage studies from a distance. These skills ensure rigorous data integrity, compliance with regulations, and effective teamwork in a remote setting.

What is a Remote Clinical Research job?

A Remote Clinical Research job involves conducting and managing clinical trials and research studies from a remote location, rather than in a traditional on-site setting. Responsibilities may include data collection, regulatory compliance, patient monitoring, and communication with study teams. These roles often use digital tools and electronic data capture systems to ensure research integrity and efficiency. Remote clinical research professionals typically work for pharmaceutical companies, contract research organizations (CROs), or healthcare institutions. This job offers flexibility while still contributing to medical advancements and patient care.

What are some unique challenges and benefits of working in a remote clinical research role?

Working remotely in clinical research often requires you to be highly independent, organized, and proficient with digital collaboration tools, as you'll be coordinating with cross-functional teams and managing regulatory documentation from a distance. One challenge can be maintaining consistent communication with clinical sites and colleagues across different time zones, but many companies provide robust digital platforms to facilitate this. On the plus side, remote roles offer flexibility and a better work-life balance while still allowing you to contribute to impactful research. Many remote clinical research professionals report developing strong self-discipline and process management skills, which can open doors to advanced positions such as Clinical Research Associate or Project Manager.

What are the most commonly searched types of Clinical Research jobs in Remote, OR? The most popular types of Clinical Research jobs in Remote, OR are:
What are popular job titles related to Remote Clinical Research jobs in Remote, OR? For Remote Clinical Research jobs in Remote, OR, the most frequently searched job titles are:
What cities near Remote, OR are hiring for Remote Clinical Research jobs? Cities near Remote, OR with the most Remote Clinical Research job openings:
Infographic showing various Remote Clinical Research job openings in Remote, OR as of July 2026, with employment types broken down into 2% Internship, 80% Full Time, 10% Part Time, 3% Temporary, and 5% Contract. Highlights an 100% Remote job distribution, with an average salary of $107,230 per year, or $51.6 per hour.

Senior Clinical Research Associate

Nexpro Technologies Inc

OR • Remote

$90K - $120K/yr

Full-time

Medical

Posted 19 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.