Clinical Research Coordinator

4 days ago


Kansas City, Missouri, United States Alcanza Clinical Research Full time
Job Description

Alcanza Clinical Research is a leading provider of clinical research services, with a strong presence across Phase I-IV studies and multiple therapeutic areas. We are seeking a highly skilled Clinical Research Coordinator to join our team.

Key Responsibilities
  • Under the direction of the Site Manager/Director and Principal/Sub Investigators, conduct clinical research studies in accordance with FDA, GCP, and ICH regulations and guidelines.
  • Screen patients for study enrollment, obtain informed consent, and conduct patient follow-up visits.
  • Document patient information in source clinic charts and enter data into electronic data capture systems.
  • Perform basic clinical procedures, such as blood pressure, vital signs, and EKGs.
  • Request and track medical records, update and maintain logs, and schedule patient visits.
  • Conduct monitoring visits, resolve issues, and ensure study-related reports are reviewed by investigators in a timely manner.
Requirements
  • Medical Assistant diploma, LPN/LVN, or EMT credential, with 1+ year of clinical research coordination experience.
  • Proficiency in computer applications, including Microsoft Office and electronic health records.
  • Strong organizational skills, attention to detail, and ability to work independently and as part of a team.
  • Excellent written and verbal communication skills, with the ability to handle sensitive information confidentially.
Benefits
  • Full-time employees are eligible for benefits, including medical, dental, vision, life insurance, and a 401(k) plan.


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