Clinical Research Coordinator I - Cardiovascular Trials

Cleveland Clinic

United States

Vor Ort

USD 52.000 - 72.000

Vollzeit

Vor 6 Tagen
Sei unter den ersten Bewerbenden

Eine vollständige Bewerbung in einer Minute

Maßgeschneiderter Lebenslauf und Anschreiben – versandbereit.

Schaffe es an den ATS-Filtern vorbei

Zusammenfassung

Cleveland Clinic seeks a Research Coordinator I NE for the Tang Lab at the Main Campus in Cleveland. You will enroll patients in clinical trials, conduct study visits, collect questionnaires, and perform research-related procedures under supervision.

You will interact with participants to explain protocols, obtain informed consent, and ensure data quality while supporting ongoing cardiovascular research and translational efforts. Training provided where needed.

Qualifikationen

  • Minimum: High School Diploma or GED and two years of clinical research or healthcare experience, or an Associate/Bachelor’s in healthcare or science.
  • Must complete Human Subjects Research certification within 90 days of hire.
  • Strong organizational, communication and interpersonal skills.

Aufgaben

  • Coordinate compliant implementation and conduct of human subject research projects.
  • Maintain regulatory documents and binders; conduct data management and IRB submissions.
  • Screen patients for study eligibility and obtain informed consent when applicable.
  • Perform phlebotomy and collect research samples; assist with study procedures and visits.
  • Communicate with sponsors, monitors, and research personnel to ensure study compliance.

Kenntnisse

Clinical research experience
IRB/compliance understanding
Communication skills
Data collection & management

Ausbildung

High School Diploma or GED
Associate’s or Bachelor’s Degree in healthcare or science

Tools

EPIC
Microsoft Office
Data management systems

Jobbeschreibung

Cleveland Clinic seeks a Research Coordinator I NE for the Tang Lab at the Main Campus in Cleveland. You will enroll patients in clinical trials, conduct study visits, collect questionnaires, and perform research-related procedures under supervision.

You will interact with participants to explain protocols, obtain informed consent, and ensure data quality while supporting ongoing cardiovascular research and translational efforts. Training provided where needed.

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