Clinical Research Coordinator

4 days ago


Kansas City, Missouri, United States U.S. Dermatology Partners Full time
Job Summary

We are seeking a highly organized and detail-oriented Clinical Research Assistant to join our team at U.S. Dermatology Partners. The successful candidate will assist with patient visits, data acquisition, and laboratory duties, ensuring the integrity and consistency of clinical trial data.

Key Responsibilities
  • Assist coordinators with patient visits, including scheduling, data acquisition, and procedures such as biopsies and photodynamic therapy.
  • Verify and maintain data integrity, adhering to study protocols and Good Clinical Practice.
  • Assist physicians with patient care and treatment, including instrument preparation and suture removal.
  • Collect EKGs and vital signs, and assist with study visits, source document completion, and case report form submission.
  • Perform laboratory duties and functions related to study protocols, ensuring compliance with IATA and OSHA standards.
  • Document clinical trial files in accordance with company standard operating procedures and study protocols.
  • Screen potential research participants and patients for enrollment, and review exclusion/inclusion criteria with the Principal Investigator or Lead Coordinator.
Requirements
  • 4 years of experience, including a Bachelor's Degree in a life science or social science, or equivalent clinical experience.
  • At least 1 year of experience directly related to the duties and responsibilities specified.
  • Meticulous attention to detail, professional attitude, and reliability.
  • Organizational skills to support accurate record-keeping, and ability to follow verbal and written instructions.
  • Interpersonal skills to work effectively with patients and outside parties, and ability to communicate effectively in English, both verbally and in writing.
Working Conditions

This position has no supervisory responsibilities and requires a working knowledge of applicable protocols, with some team members assigned as primary coordinators for specific protocols.



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