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Clinical Research Analyst Jobs (NOW HIRING)

DaVinci Research

Clinical Research Coordinator

Roseville, CA · On-site

$25.50 - $33.75/hr

Strong background in Research, including data collection and analysis * Clinical Research Experience and familiarity with Clinical Trials processes * Phlebotomy Certified * Excellent organizational ...

GAP SOLUTIONS INC

Research Analyst

Rockville, MD · On-site

$115K - $125K/yr

Conduct and analyze large, complex databases in cancer epidemiologic studies including ... Research and review literature to retrieve targeted clinical or scientific information from ...

New

Catholic Health

Research Analyst

Roslyn, NY

$26.92 - $32.30/hr

Responsibilities: * Assist clinical staff with the design of clinical/population health research ... Perform statistical analyses of datasets including descriptive analyses, survival analyses ...

Catholic Health

Research Analyst

Roslyn, NY

$26.92 - $32.30/hr

Responsibilities: * Assist clinical staff with the design of clinical/population health research ... Perform statistical analyses of datasets including descriptive analyses, survival analyses ...

Catholic Health

Research Analyst

Roslyn, NY · On-site

$26.92 - $32.30/hr

Responsibilities: * Assist clinical staff with the design of clinical/population health research ... Perform statistical analyses of datasets including descriptive analyses, survival analyses ...

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How much do clinical research analyst jobs pay per year?

As of Sep 11, 2026, the average yearly pay for clinical research analyst in the United States is $73,965.00, according to ZipRecruiter salary data. Most workers in this role earn between $57,000.00 and $98,500.00 per year, depending on experience, location, and employer.

What is a clinical research analyst?

A Clinical Research Analyst is a professional who specializes in collecting, analyzing, and interpreting data from clinical trials and medical studies. They play a crucial role in ensuring the accuracy and integrity of research data, which helps guide healthcare decisions and regulatory approvals. Their responsibilities may include designing data collection systems, monitoring study progress, and preparing reports for stakeholders. Clinical Research Analysts often work in hospitals, pharmaceutical companies, or research organizations, collaborating with scientists, doctors, and regulatory agencies.

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

To thrive as a Clinical Research Analyst, you need a solid background in life sciences or healthcare, strong analytical skills, and familiarity with clinical research methodologies, often supported by a relevant degree. Proficiency with data analysis tools such as SAS, SPSS, or R, and knowledge of regulatory systems like FDA or ICH-GCP guidelines, are typically required. Attention to detail, effective communication, and problem-solving abilities are vital soft skills for managing complex data and collaborating with research teams. These skills and qualities ensure accurate data interpretation, regulatory compliance, and successful execution of clinical studies.

What types of teams and departments do clinical research analysts typically collaborate with during a clinical trial?

Clinical Research Analysts often work cross-functionally with various teams, including clinical operations, regulatory affairs, data management, and biostatistics. They coordinate closely with principal investigators, study coordinators, and sometimes external partners like contract research organizations. This collaboration ensures that data collection, reporting, and regulatory submissions are accurate and timely. Being able to communicate effectively across disciplines is essential for success in this role.

What is the difference between Clinical Research Analyst vs Clinical Data Coordinator?

AspectClinical Research AnalystClinical Data Coordinator
Required CredentialsBachelor's degree in life sciences, certifications like CCRP or RAC often preferredBachelor's degree in health sciences, certifications like CDMP or CCRC beneficial
Work EnvironmentResearch sites, pharmaceutical companies, CROs, hospitalsClinical trial sites, hospitals, research organizations
Employer & Industry UsageUsed in clinical research, pharmaceutical, biotech industriesCommon in clinical trial management and data handling
Comparison Search IntentUnderstanding roles, responsibilities, and qualificationsFocus on data management and coordination tasks

The Clinical Research Analyst and Clinical Data Coordinator roles share similarities in their focus on clinical trials and data handling, but differ mainly in responsibilities. The analyst interprets data and supports research analysis, while the coordinator manages data collection and entry. Both roles require relevant degrees and certifications, and are vital in the clinical research industry.

Do you need a degree to be a clinical research analyst?

A clinical research analyst typically needs at least a bachelor's degree in a related field such as life sciences, healthcare, or statistics. Some positions may require additional certifications or experience with data analysis tools and clinical trial processes. Educational background and relevant skills are important for entry and advancement in this role.

Is clinical research in high demand?

Clinical research analysts are in high demand due to the ongoing need for new medical treatments and advancements in healthcare. The field offers growth opportunities, especially for those with strong analytical skills, knowledge of regulatory requirements, and experience with data management tools. Employment is expected to grow faster than average in the coming years.
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Clinical Research Analyst jobs near you
Infographic showing various Clinical Research Analyst job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 74% Full Time, 15% Part Time, and 8% Contract. Highlights an 85% Physical, 1% Hybrid, and 14% Remote job distribution, with an average salary of $73,965 per year, or $35.6 per hour.

Clinical Research Coordinator

Roseville, CA • On-site

DaVinci Research
See more jobs at DaVinci Researchexternal

$25.50 - $33.75/hr

Other

Re-posted 22 days ago

Job description

Company Description

DaVinci Research (DVR) is a leading Site Management Organization dedicated to conducting clinical research trials. In collaboration with innovative pharmaceutical and medical device companies worldwide, DVR serves as a bridge between investigators and study sponsors. The organization is committed to ensuring the successful execution of clinical trials while advancing medical knowledge. DaVinci Research operates with a strong focus on fostering innovation and improving patient outcomes through the clinical research process.


Role Description

This is a full-time, ON-SITE role for a Clinical Research Coordinator located in Roseville, CA. The Clinical Research Coordinator will be involved in the coordination and execution of clinical trials, including obtaining informed consent, ensuring compliance with study protocols, and facilitating research staff communication. Responsibilities include managing study documentation, overseeing site-specific trial activities, and ensuring adherence to regulatory and sponsor requirements.


Qualifications

  • Experience with Informed Consent and ensuring ethical standards in clinical research
  • Knowledge of study Protocols and compliance with procedural guidelines
  • Strong background in Research, including data collection and analysis
  • Clinical Research Experience and familiarity with Clinical Trials processes
  • Phlebotomy Certified
  • Excellent organizational, communication, and teamwork skills
  • Ability to work independently and efficiently in a fast-paced environment
  • Bachelor’s degree in Life Sciences, Health Sciences, or related field
  • Previous experience in a healthcare or medical research setting is a plus

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