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Clinical Trial Jobs in Remote, OR (NOW HIRING)

TechData Service Company LLC

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Biostat III - Clinical Statistical Developer (R/AI) - LPAB

OR · On-site

$80 - $85/hr

Clinical trial/statistical analysis experience * Build reusable statistical tools/modules and perform ad hoc analyses * Work directly with study teams across therapeutic areas * AI/agent experience ...

Bausch + Lomb

Director, Clinical Development

OR · On-site +1

$75K - $102K/yr

Ensure timely submission of clinical trial data to regulatory authorities. * Identify and mitigate risks associated with clinical research activities. Requirements: * Advanced degree (MD, OD, PhD, or ...

Bausch+Lomb Companies Inc.

Director, Clinical Development

OR · Remote

$81K - $111K/yr

Ensure timely submission of clinical trial data to regulatory authorities. * Identify and mitigate risks associated with clinical research activities. Requirements: * Advanced degree (MD, OD, PhD, or ...

IT ENGAGEMENTS INC

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CRA/CPM Study Start-Up and Monitoring Support (Contract Role)

OR · Remote

$68 - $70/hr

Help prepare and route Clinical Trial Agreements (CTAs) and other site contracts for CPM and Legal review. * Support site budget tracking and invoice reconciliation. * Prepare IRB/EC submission ...

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IT ENGAGEMENTS INC

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CRA/CPM Study Start-Up and Monitoring Support (Contract Role)

OR · Remote

$68 - $70/hr

Help prepare and route Clinical Trial Agreements (CTAs) and other site contracts for CPM and Legal review. * Support site budget tracking and invoice reconciliation. * Prepare IRB/EC submission ...

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Clinical Trial information

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How much do clinical trial jobs pay per hour?

As of Sep 5, 2026, the average hourly pay for clinical trial 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 are clinical trials?

Clinical trials are research studies that involve human participants and are designed to evaluate the safety and effectiveness of new medical treatments, drugs, or devices. These trials follow a carefully controlled protocol and are conducted in phases to systematically assess outcomes. Participants may include patients with specific medical conditions or healthy volunteers, depending on the study's goals. The results from clinical trials help inform medical decisions and regulatory approvals for new therapies.

What are the key skills and qualifications needed to thrive in a clinical trial role?

To thrive in a Clinical Trial role, you need a solid understanding of clinical research principles, regulatory compliance, and data management, usually supported by a degree in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) certification, and clinical trial management software is typically required. Strong attention to detail, organizational abilities, and effective communication skills help professionals coordinate complex processes and collaborate with interdisciplinary teams. These competencies are vital to ensure trials are conducted ethically, efficiently, and in compliance with regulatory standards.

What are some common challenges faced by professionals working in clinical trial management, and how can they be addressed?

Professionals in clinical trial management often encounter challenges such as adhering to strict regulatory requirements, managing complex timelines, and ensuring effective communication among multidisciplinary teams. Overcoming these challenges typically involves thorough planning, continuous training on regulatory updates, and the use of project management tools to track progress and coordinate tasks. Building strong relationships with investigators and fostering open communication can also help address issues quickly and maintain trial integrity.

How to get into a clinical trial career?

A career in clinical trials typically requires a background in healthcare, life sciences, or related fields, along with knowledge of Good Clinical Practice (GCP) guidelines. Entry-level roles often require a bachelor's degree, and certifications such as Certified Clinical Research Professional (CCRP) can enhance job prospects. Gaining experience through internships or entry-level positions in research settings is also beneficial.

What jobs are there in clinical trials?

Jobs in clinical trials include clinical research coordinators, clinical research associates, data managers, regulatory affairs specialists, and study nurses. These roles involve tasks such as patient recruitment, data collection, monitoring trial progress, and ensuring compliance with regulations, often requiring knowledge of Good Clinical Practice (GCP) and relevant certifications. The work environment is typically in hospitals, research centers, or pharmaceutical companies.

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

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

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

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

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

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

Clinical Trial jobs near you
Infographic showing various Clinical Trial job openings in Remote, OR as of August 2026, with employment types broken down into 72% Full Time, and 28% Part Time. Highlights an 55% In-person, and 45% 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 26 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.