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Clinical Research Associate Fsp Jobs in Remote, OR

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 ...

All JobsClinical Research Associate Fsp JobsClinical Research Associate Fsp Jobs in Remote, OR

Clinical Research Associate Fsp information

See Remote, OR salary details

$36K

$86.4K

$137.9K

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

As of Aug 22, 2026, the average yearly pay for clinical research associate fsp in Remote, OR is $86,370.00, according to ZipRecruiter salary data. Most workers in this role earn between $53,900.00 and $113,900.00 per year, depending on experience, location, and employer.

What is a clinical research associate FSP?

A Clinical Research Associate (CRA) FSP, or Functional Service Provider CRA, is a professional who monitors clinical trials and research studies on behalf of pharmaceutical, biotechnology, or medical device companies, but is assigned through a service provider rather than directly employed by the sponsor. Their responsibilities include ensuring compliance with study protocols, regulatory requirements, and data integrity, as well as site management and reporting. CRAs in FSP models often work across multiple projects and organizations, providing flexibility and specialized expertise to sponsors while gaining broad experience in clinical research operations.

What are the key skills and qualifications needed to thrive as a clinical research associate FSP?

To thrive as a Clinical Research Associate (FSP), you need a solid background in life sciences or a related field, knowledge of Good Clinical Practice (GCP), and experience in clinical trial monitoring. Familiarity with electronic data capture (EDC) systems, regulatory documentation software, and certifications such as GCP or CRA certification are typically required. Strong organizational skills, attention to detail, and excellent communication enable effective site management and collaboration with diverse stakeholders. These competencies ensure compliance, data integrity, and successful execution of clinical studies.

What are some common challenges faced by clinical research associates FSP when monitoring multiple study sites, and how can these be managed effectively?

Clinical Research Associates (FSP) often juggle multiple study sites, each with its own protocols, staff, and logistical hurdles. Common challenges include coordinating communication across sites, ensuring consistent protocol adherence, and managing travel or remote monitoring schedules. Effective organization, clear documentation, and proactive communication with site staff are key to overcoming these challenges. Utilizing centralized tracking tools and regularly scheduled check-ins can greatly enhance oversight and help maintain high-quality data collection across all assigned sites.

How much does a clinical research associate Fsp get paid?

A Clinical Research Associate FSP (Functional Service Provider) typically earns between $70,000 and $110,000 annually, depending on experience, location, and the complexity of the trials. Compensation may also include bonuses and benefits, with some roles offering flexible schedules and remote work options.

Is it hard to get a clinical research associate Fsp job?

Securing a Clinical Research Associate FSP (Full-Service Provider) role can be competitive, often requiring relevant experience in clinical trials, knowledge of Good Clinical Practice (GCP), and strong organizational skills. Candidates with certifications such as CCRP or RAC and familiarity with clinical trial management systems tend to have better prospects. The difficulty varies based on individual qualifications and market demand.

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

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

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

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

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

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

Clinical Research Associate Fsp jobs near you
Infographic showing various Clinical Research Associate Fsp job openings in Remote, OR as of August 2026, with employment types broken down into 1% As Needed, 70% Full Time, 25% Part Time, 1% Temporary, and 3% Contract. Highlights an 82% Physical, 1% Hybrid, and 17% Remote job distribution, with an average salary of $86,370 per year, or $41.5 per hour.

Senior Clinical Research Associate

Nexpro Technologies Inc

OR • Remote

$90K - $120K/yr

Full-time

Medical

Re-posted 12 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.