Clinical Research Coordinator I Or Ii - Orthopedics

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Crc i: $49,000 annually; crc ii: $55,000 annually;...
Fully remote
Participant recruitment and screening
Eligibility determination and enrollment
Study protocol adherence
These positions offer the opportunity to collaborate with nationally recognized investigators and multidisciplinary teams to advance innovative, patient-centered research across a wide range of musculoskeletal specialties

Job Summary

  • These positions offer the opportunity to collaborate with nationally recognized investigators and multidisciplinary teams to advance innovative, patient-centered research across a wide range of musculoskeletal specialties.
  • One position will support the Orthopedic Trauma Research Program, coordinating multiple ongoing, multi-center clinical trials in a fast-paced clinical setting, with direct collaboration with six orthopedic trauma surgeons.
  • The second position will support department-wide clinical research initiatives across multiple orthopedic subspecialties, coordinating multi-site clinical study activities and supporting internal quality and compliance efforts.

Matching Summary

These positions offer the opportunity to collaborate with nationally recognized investigators and multidisciplinary teams to advance innovative, patient-centered research across a wide range of musculoskeletal specialties.

Salary

CRC I: $49,000 annually; CRC II: $55,000 annually; Benefits: generous vacation, holidays, and sick leave; competitive insurances and savings accounts; retirement benefits

Skills & Requirements

Must-have

  • Participant recruitment and screening
  • Eligibility determination and enrollment
  • Study protocol adherence
  • Regulatory compliance
  • Data and sample management
  • Patient-facing activities

Nice-to-have

  • Manuscript preparation and grant development
  • Mentoring medical students and residents
  • Internal quality and compliance efforts
  • Continuous improvement of research infrastructure

Key Requirements

  • 0-2 years clinical research experience (CRC I)
  • 2 years clinical research experience (CRC II)
  • Human subjects research experience
  • Prior experience adhering to IRB approved protocols
  • Prior experience with data entry
  • Prior experience with EMR or EHR systems
  • Prior experience consenting and enrolling human subjects (CRC II)
  • Prior experience with FDA regulated clinical trials (CRC II)
  • Prior experience with EDC systems (CRC II)
  • Prior experience with CTMS (CRC II)
  • Prior experience managing multiple research projects (CRC II)

Work Rights

Must be authorized to work in the US without sponsorship

Tailored Resume

Cover Letter