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Clinical Trials Jobs in Remote, OR (NOW HIRING)

VieMed

Perm - NP/PA - Oncology Coos Bay, OR

Coos Bay, OR · On-site

$135K/yr

Participate in clinical trials and cancer support services * Maintain accurate documentation in electronic medical records (EPIC) * Support the hospital's commitment to compassionate, evidence-based ...

Bausch+Lomb Companies Inc.

Director, Clinical Development

OR · Remote

$81K - $111K/yr

Design and oversee clinical trials including feasibility, pivotal, and post-approval studies across diverse markets. * Set direction and ensure alignment of clinical research priorities with company ...

Bausch + Lomb

Director, Clinical Development

OR · On-site +1

$75K - $102K/yr

Design and oversee clinical trials including feasibility, pivotal, and post-approval studies across diverse markets. * Set direction and ensure alignment of clinical research priorities with company ...

MedExcellence

Perm - Oncology - NP / PA

Coos Bay, OR · On-site

Provide services including radiation therapy, chemotherapy, medical oncology, cancer support services, and clinical trials. * Utilize a new 19-chair infusion room, in-house pharmacy, nurse navigation ...

MedExcellence

Perm - Oncology - MD/DO

Coos Bay, OR · On-site

$189.25/hr

Engage in leading-edge clinical trials and innovative treatment approaches. * Provide comprehensive cancer care in a state-of-the-art facility. * Contribute to a family-oriented environment and ...

She Recruits LLC

Oncology Nurse Practitioner

Coos Bay, OR · On-site

$135K/yr

Cancer support services and clinical trials * A newly designed 19-chair infusion room * In-house pharmacy, nurse navigation, and radiation oncology * Onsite lab services * A highly skilled, collegial ...

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All JobsClinical Trials JobsClinical Trials Jobs in Remote, OR

Clinical Trials information

See Remote, OR salary details

$28

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How much do clinical trials jobs pay per hour?

As of Aug 26, 2026, the average hourly pay for clinical trials in Remote, OR is $62.45, according to ZipRecruiter salary data. Most workers in this role earn between $50.67 and $70.38 per hour, depending on experience, location, and employer.

What is a clinical trial?

A Clinical Trials job involves managing, coordinating, or supporting research studies that evaluate the safety and effectiveness of medical treatments, drugs, or devices. Professionals in this field work on trial design, patient recruitment, data collection, regulatory compliance, and reporting results. Roles can range from clinical research coordinators to trial managers and regulatory specialists. The goal is to ensure that studies follow ethical guidelines and produce reliable data for medical advancements.

What are some common career paths or advancement opportunities for professionals working in clinical trials?

Many professionals in Clinical Trials start their careers as Clinical Research Coordinators, Clinical Research Associates, or Data Managers. With experience, you can advance to roles such as Senior Clinical Research Associate, Clinical Trial Manager, or Project Manager, and potentially move into areas like regulatory affairs, medical writing, or quality assurance. The role offers continuous learning opportunities, exposure to innovative therapies, and often provides the chance to lead larger, more complex studies as you progress. Advancement is typically supported by additional certifications, strong performance, and a proactive approach to professional development. Teamwork and networking within the industry can also open new doors for growth.

What are the key skills and qualifications needed to thrive in a clinical trials position, and why are they important?

To thrive in Clinical Trials roles, you need a strong understanding of clinical research principles, Good Clinical Practice (GCP) guidelines, and a background in life sciences or healthcare. Familiarity with electronic data capture (EDC) systems, regulatory compliance software, and relevant certifications such as GCP or CCRA is highly valuable. Attention to detail, organizational skills, and effective communication enable collaboration across multidisciplinary teams. These competencies are crucial for ensuring protocol adherence, data integrity, and the successful execution of trial activities.

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

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

What are popular job titles related to Clinical Trials jobs in Remote, OR?

For Clinical Trials jobs in Remote, OR, the most frequently searched job titles are:

What job categories do people searching Clinical Trials jobs in Remote, OR look for?

The top searched job categories for Clinical Trials jobs in Remote, OR are:

What cities near Remote, OR are hiring for Clinical Trials jobs?

Cities near Remote, OR with the most Clinical Trials job openings:

Clinical Trials jobs near you
Infographic showing various Clinical Trials job openings in Remote, OR as of August 2026, with employment types broken down into 2% As Needed, 77% Full Time, 14% Part Time, and 7% Contract. Highlights an 70% Physical, 1% Hybrid, and 29% Remote job distribution, with an average salary of $129,906 per year, or $62.5 per hour.

Senior Clinical Research Associate

Nexpro Technologies Inc

OR • Remote

$90K - $120K/yr

Full-time

Medical

Re-posted 17 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.