Clinical Research Assistant - Data, Samples & Coordination

Intermountain Healthcare Inc.

Murray (UT)

On-site

USD 26,000 - 36,000

Full time

9 hours ago
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Job summary

Intermountain Healthcare seeks a research support professional to assist in duties related to clinical research and studies. You will support clinical research coordinators, investigators, physicians, nurses, and staff in data entry, documentation, and record-keeping.

Responsibilities include sample management, scheduling visits, prescreening by reviewing medical records, and assisting with consent processes in various study types while adhering to FDA GCP and SOPs.

Qualifications

  • Experience using basic computer programs including word processing, databases, spreadsheets and e-mail.

Responsibilities

  • Assist with prescreening activities by reviewing medical records of potential participants.
  • Data entry and documentation into Intermountain departmental and study-related external programs.
  • Maintain research records in accordance with policies and regulations; archive records at study closure.
  • Schedule monitoring and vendor visits and manage study kit inventory.
  • Prepare for and organize upcoming research procedures according to study protocols and assist regulatory team as requested.
  • Assist with obtaining research consent for patients on registry, observational, biospecimen, or other low-risk studies.

Skills

Teamwork
Organization
Prioritization
Adaptability
Continuous learner
Critical thinking
Self-motivation
Written and Verbal Communication
Time Management
Research

Job description

Intermountain Healthcare seeks a research support professional to assist in duties related to clinical research and studies. You will support clinical research coordinators, investigators, physicians, nurses, and staff in data entry, documentation, and record-keeping.

Responsibilities include sample management, scheduling visits, prescreening by reviewing medical records, and assisting with consent processes in various study types while adhering to FDA GCP and SOPs.

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