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Associate Clinical Data Analyst Jobs in Remote, OR

Team8

Bluespine-Sr. FWA Analyst

OR · On-site +1

Support engineering and data science teams with audit and FWA concepts, data mapping, and defining ... Medical/clinical background. * Experience with Pharma claims. * Billing/coding experience.

Sapiens

Associate Business Analyst

OR · On-site +1

Position Summary The Associate Business Analyst works under guided supervision to support the ... With agile intelligence, Sapiens' solutions turn real-time data and human insight into precise ...

SOSi

Senior Data Scientist

OR · On-site

The contractor shall provide a Rough Order of Magnitude (ROM) Estimate Report before each analytics ... Azure Data Scientist Associate, or TensorFlow Developer Certification. Additional Information Work ...

SOSi

Senior Data Scientist

Myrtle Point, OR

The contractor shall provide a Rough Order of Magnitude (ROM) Estimate Report before each analytics ... Azure Data Scientist Associate, or TensorFlow Developer Certification. Additional Information Work ...

SOSi

Senior Data Scientist

OR · On-site +1

The contractor shall provide a Rough Order of Magnitude (ROM) Estimate Report before each analytics ... Azure Data Scientist Associate, or TensorFlow Developer Certification. Additional Information Work ...

EM Key Solutions Inc

Temporary Senior Business Analyst

OR · On-site +1

$86K - $112K/yr

Understanding project architecture, test environment, test data needs based on the System build ... Four years of relevant experience or an associate degree plus two years of relevant experience may ...

Bausch + Lomb

Research Fellow, Pharma Toxicology

OR · On-site +1

$150K - $200K/yr

Oversee the generation, interpretation, and communication of essential nonclinical data to enable ... Analytical Chemistry, Regulatory Affairs, Quality, and Compliance-to support program objectives.

Agfa

Customer Support Analyst, Tier 1

OR · Remote

... data management. From product development to implementation, our unified Enterprise Imaging ... deliver clinical value. We use our proven track record as an innovator, our in-depth medical ...

AGFA

Customer Support Analyst, Tier 1

OR · On-site +1

... data management. From product development to implementation, our unified Enterprise Imaging ... deliver clinical value. We use our proven track record as an innovator, our in-depth medical ...

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All JobsAssociate Clinical Data Analyst JobsAssociate Clinical Data Analyst Jobs in Remote, OR

Associate Clinical Data Analyst information

See Remote, OR salary details

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How much do associate clinical data analyst jobs pay per hour?

As of Aug 2, 2026, the average hourly pay for associate clinical data analyst in Remote, OR is $36.32, according to ZipRecruiter salary data. Most workers in this role earn between $29.28 and $42.02 per hour, depending on experience, location, and employer.

What does a clinical data analyst do?

A clinical data analyst is responsible for collecting, managing, and analyzing healthcare data to support clinical research and decision-making. They use tools like SQL and statistical software to ensure data accuracy, generate reports, and help improve patient outcomes and research efficiency.

Is 40 too late for data science?

Age is not a barrier to becoming an Associate Clinical Data Analyst or entering data science. Many professionals successfully transition into data roles later in their careers by acquiring relevant skills such as data analysis, programming, and familiarity with tools like SQL and Python, often through certifications or training programs. Employers value experience and skills over age, making it possible to start or switch careers at 40 or older.

What does a clinical data associate do?

A clinical data associate is responsible for collecting, managing, and ensuring the accuracy of clinical trial data. They often use data management tools and work closely with research teams to support data quality and compliance with regulatory standards.

What does an Associate Clinical Data Analyst do?

An Associate Clinical Data Analyst is responsible for collecting, managing, and analyzing clinical trial data to ensure its accuracy, integrity, and compliance with regulatory standards. They typically work closely with clinical research teams to support data entry, data cleaning, and the preparation of reports. Their work is essential in helping organizations make informed decisions about the safety and efficacy of medical treatments, devices, or drugs. This entry-level role often serves as a foundation for more advanced positions in clinical data management or biostatistics.

What are some common challenges faced by Associate Clinical Data Analysts when working with clinical trial data?

Associate Clinical Data Analysts often encounter challenges such as managing large volumes of complex clinical trial data, ensuring data accuracy and consistency, and adhering to strict regulatory standards. They may also need to resolve discrepancies found during data cleaning and work collaboratively with clinical research teams to clarify ambiguous data points. Staying organized and maintaining clear communication with colleagues are key to overcoming these challenges and ensuring high-quality data for analysis.

What does an associate data analyst do?

An associate clinical data analyst collects, manages, and analyzes healthcare data to support clinical research and decision-making. They use tools like Excel and statistical software, ensure data accuracy, and follow regulatory standards to assist senior analysts and researchers in interpreting data findings.

What are the key skills and qualifications needed to thrive as an Associate Clinical Data Analyst, and why are they important?

To thrive as an Associate Clinical Data Analyst, you need a solid background in life sciences, statistics, or a related field, often supported by a bachelor’s degree. Familiarity with data management systems like EDC (Electronic Data Capture), statistical software such as SAS or R, and regulatory standards is typically required. Attention to detail, analytical thinking, and effective communication are crucial soft skills for interpreting data and collaborating with cross-functional teams. These competencies ensure accurate data analysis, regulatory compliance, and the successful execution of clinical research studies.
What are the most commonly searched types of Clinical Data Analyst jobs in Remote, OR? The most popular types of Clinical Data Analyst jobs in Remote, OR are:
What are popular job titles related to Associate Clinical Data Analyst jobs in Remote, OR? For Associate Clinical Data Analyst jobs in Remote, OR, the most frequently searched job titles are:
What job categories do people searching Associate Clinical Data Analyst jobs in Remote, OR look for? The top searched job categories for Associate Clinical Data Analyst jobs in Remote, OR are:
What cities near Remote, OR are hiring for Associate Clinical Data Analyst jobs? Cities near Remote, OR with the most Associate Clinical Data Analyst job openings:
Associate Clinical Data Analyst jobs near you
Infographic showing various Associate Clinical Data Analyst job openings in Remote, OR as of July 2026, with employment types broken down into 68% Full Time, 6% Part Time, and 26% Contract. Highlights an 60% Physical, 4% Hybrid, and 36% Remote job distribution, with an average salary of $75,550 per year, or $36.3 per hour.

Senior Clinical Research Associate

Nexpro Technologies Inc

OR • Remote

$90K - $120K/yr

Full-time

Medical

Posted 22 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.