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Clinical Research Coordinator Rpn Jobs (NOW HIRING)

DaVinci Research

Clinical Research Coordinator

Roseville, CA · On-site

$25.50 - $33.75/hr

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 ...

Alcanza Clinical Research

$23.50 - $31.25/hr

The Clinical Research Coordinator under the direction of the Site Manager/Director and the Principal/Sub Investigators conducts the following according to the study protocol, company processes ...

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As of Sep 10, 2026, the average hourly pay for clinical research coordinator rpn in the United States is $28.69, according to ZipRecruiter salary data. Most workers in this role earn between $23.32 and $31.01 per hour, depending on experience, location, and employer.

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Clinical Research Coordinator

Roseville, CA • On-site

DaVinci Research
See more jobs at DaVinci Researchexternal

$25.50 - $33.75/hr

Other

Re-posted 21 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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