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DS Research

Clinical Research Coordinator

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What they do

A Clinical Research Coordinator directs clinical research and development projects for companies, and coordinates testing and quality control.

$114,229 / year median in Kentucky

+16% projected growth

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Job Description

Clinical Research Coordinator DS Research Louisville, KY Job Details Full-time 19 hours ago Benefits Health insurance Paid time off Qualifications Electronic health records (EHR) management HIPAA Bachelor's degree Clinical data entry Attention to detail Data entry Organizational skills Patient interaction Medical terminology
Full Job Description Job Overview:
We are seeking a highly motivated and detail-oriented Clinical Research Coordinator to join our DS Research team. As a Clinical Research Coordinator, you will play a crucial role in the planning, implementation, and coordination of clinical research studies. You will work closely with the research team to ensure compliance with study protocols and regulatory requirements.
Responsibilities:
  • Coordinate and oversee all aspects of clinical trials from start-up to close-out
  • Recruit and screen potential study participants
  • Obtain informed consent from participants and ensure their understanding of study procedures
  • Collect and record accurate data during study visits
  • Monitor and document participant safety and adverse events
  • Perform vital signs measurements, blood sampling, and other clinical assessments as required
  • Maintain study documentation in accordance with Good Clinical Practice (GCP) guidelines
  • Assist with the preparation of study reports and presentations
  • Collaborate with investigators, sponsors, and other stakeholders to ensure study milestones are met
  • Ensure compliance with ethical standards, HIPAA regulations, and institutional policies
Requirements:
  • Bachelor's degree in a health-related field or equivalent experience (preferred)
  • Minimum of 2 years of experience in clinical research coordination (preferred)
  • Strong knowledge of clinical development processes and regulations
  • Proficiency in medical terminology and ability to analyze complex medical data
  • Excellent organizational skills with attention to detail
  • Ability to work independently and collaboratively and effectively communicate with patients, physicians, and research sponsors
  • Familiarity with electronic data capture systems and electronic medical records
  • Certification in Good Clinical Practice (preferred)
  • Phlebotomy and lab processing experience (preferred) We offer competitive compensation. This is an in-person, Monday
  • Thursday position.
Benefits:
Health insurance Paid time off
Medical Specialty:
Dermatology Ability to
Relocate:
Louisville, KY:
Relocate before starting work (Required)
Work Location:
In person