Clinical Research Coordinator
On-site · Gilbert, Arizona, United States
Job Summary
Clinical Research Coordinator responsible for coordinating and managing clinical trials under PI guidance, ensuring compliance with IRB, FDA, and GCP; maintaining data integrity and regulatory documents; overseeing recruitment, screening, consent, and enrollment; coordinating study visits and protocol-specific assessments; tracking adverse events; managing CTMS and study records; and collaborating with clinicians and researchers. Requires 2–3 years of clinical research experience, preferred associate or bachelor’s degree in a related field, familiarity with electronic data capture (e.g., Redcap, Medidata Rave), strong medical terminology knowledge, and proficient communication in English. Travel between Gilbert, AZ locations may be required.
Required Qualifications
- Minimum of 2–3 years of clinical research experience required.
- Associate or bachelor’s degree in biological science, healthcare, or related medical/scientific field preferred.
- Experience with electronic data capture systems (e.g., Redcap, Medidata Rave) preferred.
- Proficiency in Microsoft Office Suite (Word, Excel, Outlook).
- Strong command of medical terminology and effective oral and written communication skills.
- Ability to read, write, and communicate effectively in English.
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