On-Site Clinical Research Coordinator & Study Lead

11500 Research and Grants

United States

Vor Ort

USD 34.000 - 55.000

Vollzeit

Vor 3 Tagen
Sei unter den ersten Bewerbenden

Eine vollständige Bewerbung in einer Minute

Maßgeschneiderter Lebenslauf und Anschreiben – versandbereit.

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Benefits dieser Stelle

Benefits package
Continuing education support

Zusammenfassung

Intermountain Health is seeking a Subject Matter Expert in clinical research to coordinate studies across the system. You will collaborate with investigators, physicians and sponsors to ensure compliant execution and high-quality participant care.

Responsibilities include training, protocol dissemination and oversight of regulatory adherence. Requires experience in healthcare or research settings, proficiency with Microsoft tools, and strong organizational and communication skills.

Qualifikationen

  • Experience in healthcare, academics or research settings.
  • Proficiency with Microsoft and database applications.
  • Familiarity with laboratory protocols and documentation techniques.

Aufgaben

  • Coordinate and manage clinical studies across Intermountain system.
  • Mentor Clinical Research Coordinators and train on study protocols.
  • Educate teams about protocols, timelines and regulatory requirements.
  • Ensure compliance with GCP, SOPs and federal regulations.
  • Support participant recruitment, data entry and study quality checks.
  • Collect, process and ship lab samples as needed.

Kenntnisse

Research Protocols
Independent worker
Critical thinking
Detail-oriented
Communication skills
Organizational skills
Documentation
Verbal and written communication
Clinical information systems

Ausbildung

Bachelor's Degree in clinical life science

Jobbeschreibung

Intermountain Health is seeking a Subject Matter Expert in clinical research to coordinate studies across the system. You will collaborate with investigators, physicians and sponsors to ensure compliant execution and high-quality participant care.

Responsibilities include training, protocol dissemination and oversight of regulatory adherence. Requires experience in healthcare or research settings, proficiency with Microsoft tools, and strong organizational and communication skills.

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