Pediatric Neuro Research Coordinator

University of Utah Health Research

Salt Lake City (UT)

In loco

USD 39.000 - 68.000

Tempo pieno

30 ore fa
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Descrizione del lavoro

The University of Utah Health is seeking a detail-oriented Clinical Research Coordinator in the Pediatric Neurosurgery division on campus in Salt Lake City. This benefited staff role supports administrative and operational study activities while ensuring compliance with applicable guidelines.

You will assist investigators, coordinate study visits, manage regulatory documents, and support study data capture using systems like EPIC and REDCap.

Competenze

  • Bachelor's degree in a health sciences or related field with two years of research experience.
  • Completion of University RATS Clinical Certification within one year of hire.
  • Excellent organizational, attention to detail, and communication skills.

Mansioni

  • Assist Principal Investigators in achieving study objectives by implementing and completing study protocols and procedures.
  • Ensure proper collection, processing and shipment of specimens from OR, clinic or outpatient lab.
  • Coordinate and recruit participants, obtain informed consent, answer inquiries, schedule visits, and liaise between participants and study team.
  • Complete electronic case report forms using verified source documents and respond to sponsor queries.
  • Maintain accurate and complete research records and documentation related to procedures and devices.
  • May assist in design and preparation of research projects.
  • Assist with regulatory documents, submissions, and reports to agencies.

Conoscenze

Organizational skills
Attention to detail
Communication skills

Formazione

Bachelor's degree in health sciences
University RATS Clinical Certification

Strumenti

EPIC
REDCap

Descrizione del lavoro

The University of Utah Health is seeking a detail-oriented Clinical Research Coordinator in the Pediatric Neurosurgery division on campus in Salt Lake City. This benefited staff role supports administrative and operational study activities while ensuring compliance with applicable guidelines.

You will assist investigators, coordinate study visits, manage regulatory documents, and support study data capture using systems like EPIC and REDCap.

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