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Clinical Data Analyst Intern Jobs in Remote, OR (NOW HIRING)

Arista Networks

Internal Audit Intern - Accounting & Finance

OR · On-site +1

$16.75 - $21.75/hr

The Internal Audit team is seeking a graduate-level intern with a strong accounting and finance ... Analyze financial data to identify trends, anomalies, and potential risk areas * Document business ...

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.

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 ...

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.

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 ... care/clinical business processes are preferred but not mandatory. * Experience using risk-based ...

Aviva Health

Clinical Quality Manager

Roseburg, OR · On-site

$50.61 - $61.85/hr

The Clinical Quality Manager collaborates with providers, other clinical departments and operations ... Analyzing data utilizing risk stratification tools per PCPCH requirements to maintain 5-star ...

Aviva Health

Clinical Quality Manager

Roseburg, OR · On-site

$50.61 - $61.85/hr

The Clinical Quality Manager collaborates with providers, other clinical departments and operations ... Analyzing data utilizing risk stratification tools per PCPCH requirements to maintain 5-star ...

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All JobsClinical Data Analyst Intern JobsClinical Data Analyst Intern Jobs in Remote, OR

Clinical Data Analyst Intern information

See Remote, OR salary details

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

As of Aug 6, 2026, the average hourly pay for clinical data analyst intern in Remote, OR is $22.48, according to ZipRecruiter salary data. Most workers in this role earn between $17.31 and $24.47 per hour, depending on experience, location, and employer.

What does a clinical data analyst intern do?

A Clinical Data Analyst Intern assists in managing and analyzing clinical trial data to ensure its accuracy, integrity, and compliance with regulatory standards. They work closely with data managers, statisticians, and clinical research teams to clean, validate, and interpret data from clinical studies. Interns may also be involved in preparing reports, maintaining databases, and supporting the development of data collection tools. This role provides valuable experience in data management, clinical research, and the use of specialized software in the healthcare industry.

What are the key skills and qualifications needed to thrive as a clinical data analyst intern?

To thrive as a Clinical Data Analyst Intern, you need a solid background in statistics, data analysis, and healthcare concepts, often supported by coursework in public health, biostatistics, or related fields. Familiarity with tools like SQL, SAS, R, or Python and experience working with electronic health records (EHRs) and data visualization platforms are highly valuable. Attention to detail, strong problem-solving skills, and clear communication help you interpret complex data and collaborate with multidisciplinary teams. These abilities are essential for ensuring accurate data insights, supporting clinical decision-making, and driving improvements in healthcare outcomes.
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Clinical Data Analyst Intern jobs near you

Senior Clinical Research Associate

Nexpro Technologies Inc

OR • Remote

$90K - $120K/yr

Full-time

Medical

Posted 27 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.