Part-Time

Temporary Clinical Research Coordinator

Surgery

Posted on 9/26/2025

Deadline 10/7/25
University of Louisville

University of Louisville

No salary listed

Company Does Not Provide H1B Sponsorship

Louisville, KY, USA

In Person

Assistance and accommodations are available at the Human Resources Department located at 215 Central Avenue, Ste 205 - Louisville, Kentucky 40208.

Category
Biology & Biotech (4)
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Requirements
  • Four or more years experience or an equivalent combination of education and experience.
Responsibilities
  • Facilitates compliance with the research protocol and Good Clinical Practice guidelines.
  • Uses multiple communication styles and methods to facilitate the effective coordination of clinical trials across disciplines and clinics, acting as a liaison between the principle investigator, sponsoring agent, study patients, referring physicians, pharmacist, statisticians and other members of the research team.
  • Takes leadership in ensuring an effective informed-consent process and study subject safety for the duration of the trial.
  • Ensures compliance with protocol procedures, assessments and reporting requirements.
  • Assists physicians in ensuring adequate source documentation and data-collection that validate the integrity of the clinical trial.
  • Assist in enhancing recruitment of study participants, helping with the design and implementation of recruitment strategies for identifying and assessing patients who may be eligible for a clinical trial.
  • Demonstrates leadership in adhering to ethical principles in the conduct of clinical trials in order to protect study subjects and data integrity.
Desired Qualifications
  • Experience in Clinical Research.
  • Experience in device, hepatic arterial, and drug based clinical research.
University of Louisville

University of Louisville

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