Research Services Entry Professional

University of Colorado
Hybrid

About The Position

This position is a research assistant at the Steadman Hawkins Inverness UCHealth clinic. Research assistants perform research related functions which may include patient- oriented research or research conducted with human subjects. Patient-oriented research includes mechanisms of human disease, therapeutic interventions, clinical trials, or development of new technologies. Research assistants may also assist with epidemiologic and behavioral studies, biomechanics studies, and/or outcomes research and health services research.

Requirements

  • Bachelor’s degree in any field
  • A combination of education and related technical/military/paraprofessional experience may be substituted for a bachelor’s degree on a year for year basis.
  • Knowledge and understanding of federal regulations and Good Clinical Practice (GCP)
  • Ability to communicate effectively, both in writing and orally
  • Ability to establish and maintain effective working relationships with employees at all levels throughout the institution
  • Outstanding customer service skills
  • Knowledge of basic human anatomy, physiology medical terminology
  • Ability to interpret and master complex research protocol information

Nice To Haves

  • Bachelor’s degree in science or health related field
  • Clinical research or related experience
  • Experience with electronic data capture systems (e.g. EMR or EHR and data management systems)

Responsibilities

  • Support senior research staff and principal investigators (PIs) with new and ongoing research projects, contributing to various aspects of study execution.
  • Support clinical trials by assisting with study start-up, managing timelines, tracking study progress, and assisting with regulatory submissions.
  • Maintain compliance with FDA regulations, IRB requirements, and institutional policies.
  • Conduct chart reviews to extract relevant clinical data for retrospective research studies and confirm participant eligibility
  • Perform informed consent for prospective research studies.
  • Coordinate patient visits in adherence to study protocols including scheduling, data collection, and follow up.
  • Perform data entry to ensure accurate and timely documentation of research findings.
  • Ensure data quality control by verifying accuracy and completeness of collected data.
  • Collect and analyze clinical research data to support study objectives and outcomes assessment.
  • Maintain detailed research records to ensure protocol adherence and data integrity.
  • Coordinate with sponsors, researchers, and clinical staff to facilitate study procedures and ensure smooth execution of research protocols
  • Attend regular meetings with study investigators and provide progress reports on study status, challenges, and key milestones.

Benefits

  • Medical: Multiple plan options
  • Dental: Multiple plan options
  • Additional Insurance: Disability, Life, Vision
  • Retirement 401(a) Plan: Employer contributes 10%25 of your gross pay
  • Vacation Days: 22/year (maximum accrual 352 hours)
  • Sick Days: 15/year (unlimited maximum accrual)
  • Holiday Days: 10/year
  • Tuition Benefit: Employees have access to this benefit on all CU campuses
  • ECO Pass: Reduced rate RTD Bus and light rail service
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