What are the responsibilities and job description for the Clinical Research Coordinator position at DaVinci Research?
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