ZipRecruiter

Log In

1

Senior Clinical Research Associate Jobs in Remote, OR

Servier

Senior Manager, Privacy

OR · On-site +1

$160 - $180K/hr

Reporting to the Sr. Director, US Head of Data Privacy, this Senior Manager level professional will ... Clinical, R&D, Market Research, Commercial Marketing, and Commercial Operations This position ...

Amgen, Inc.

Biostatistical Programming Senior Manager

OR · On-site +1

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 ...

Brookdale Senior Living, Inc.

Caregiver

Roseburg, OR · On-site

$13.75 - $17.25/hr

Associate assistance program * Employee discounts * Referral program * Early access to earned wages ... Industry leader in clinical care. * Nationwide company with 589 communities as of November 30, 2025 ...

AGFA

Senior Project Manager

OR · On-site +1

... clinical, operational and business strategies. The Senior Project Manager must plan, execute ... CAPM (Certified Associate in Project Management) will be considered along with overall project ...

Agfa

Senior Project Manager

OR · Remote

... clinical, operational and business strategies. The Senior Project Manager must plan, execute ... CAPM (Certified Associate in Project Management) will be considered along with overall project ...

next page

Showing results 1-20

All JobsClinical Research Associate JobsSenior Clinical Research Associate JobsSenior Clinical Research Associate Jobs in Remote, OR

Senior Clinical Research Associate information

See Remote, OR salary details

$36K

$94.2K

$143.4K

How much do senior clinical research associate jobs pay per year?

As of Aug 25, 2026, the average yearly pay for senior clinical research associate in Remote, OR is $94,221.00, according to ZipRecruiter salary data. Most workers in this role earn between $62,400.00 and $127,900.00 per year, depending on experience, location, and employer.

What does a senior clinical research associate do?

A senior clinical research associate (CRA) monitors clinical trials and manages team members. Your duties include leading project team meetings, running experiments, making observations, tracking results, and analyzing data. You also ensure experiments meet all clinical practice and safety standards. Qualifications for this career are a bachelor of science in a biomedical field or a bachelor of science in nursing (BSN), along with professional experience in a medical or research setting. You must have strong communication, interpersonal, leadership, and technical writing skills.

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

To thrive as a Senior Clinical Research Associate, you need a solid background in clinical research, regulatory compliance, and often a degree in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) guidelines, and relevant certifications such as ACRP or SOCRA are typically required. Strong organizational skills, attention to detail, and the ability to communicate effectively with diverse stakeholders make someone stand out in this position. These skills and qualities are vital for ensuring studies are conducted ethically, accurately, and in compliance with regulatory standards.

What are some typical challenges faced by senior clinical research associates when overseeing multiple clinical trials?

Senior Clinical Research Associates (SCRAs) often manage several studies at once, which requires balancing competing deadlines, ensuring protocol compliance, and maintaining strong communication with site staff. A common challenge is ensuring consistent data quality and regulatory adherence across diverse sites, especially when trials are geographically dispersed. Effective time management, attention to detail, and proactive problem-solving are crucial for success in this role. Collaboration with project managers, investigators, and regulatory teams is also essential to ensure trials progress smoothly and meet all regulatory requirements.
More about Senior Clinical Research Associate jobs

What are popular job titles related to Senior Clinical Research Associate jobs in Remote, OR?

For Senior Clinical Research Associate jobs in Remote, OR, the most frequently searched job titles are:

What job categories do people searching Senior Clinical Research Associate jobs in Remote, OR look for?

The top searched job categories for Senior Clinical Research Associate jobs in Remote, OR are:

What cities near Remote, OR are hiring for Senior Clinical Research Associate jobs?

Cities near Remote, OR with the most Senior Clinical Research Associate job openings:

Senior Clinical Research Associate jobs near you
Infographic showing various Senior Clinical Research Associate 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 $94,221 per year, or $45.3 per hour.

Senior Clinical Research Associate

OR • Remote

Nexpro Technologies Inc
See more jobs at Nexpro Technologies Incexternal

$90K - $120K/yr

Full-time

Medical

Re-posted 15 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.