Arthroplasty Clinical Research Coordinator

Hospital for Special Surgery

New York, Northern (NY, KY)

Hybrid

USD 65,000 - 95,000

Full time

13 days ago
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Job summary

Hospital for Special Surgery seeks a Clinical Research Coordinator to join the Arthroplasty Service research team. The role supports day-to-day research activities, patient coordination, and data management ensuring efficient operations and regulatory compliance.

The coordinator will work under the Arthroplasty Director, participate in protocol development, and assist with enrollment, data collection, and IRB documentation while supporting other research staff in a collaborative setting.

Qualifications

  • Bachelor's degree required; Master's preferred.
  • 3+ years of clinical research experience.
  • Prior Epic experience.
  • Knowledge of Good Clinical Practice and Good Technology Practice.
  • Proficient with computers and software.
  • Knowledge of Orthopaedic/Rheumatologic terminology is a plus.

Responsibilities

  • Coordinate research activities within ARJR under the Director's oversight.
  • Supervise study staff and act as primary contact for study activities.
  • Provide administrative support for registry and clinical research tasks.
  • Generate regular reports for the Director, IRB, PI, NIH, and sponsors.
  • Contribute to protocol development and data collection forms.
  • Ensure compliance with regulatory, institutional, and departmental requirements.
  • Assist in patient care coordination and enrollment/log maintenance.
  • Support training and documentation for research staff.

Skills

Clinical Research Coordination
Epic experience
Regulatory compliance
Data management
Communication

Education

Bachelor's degree
Masters preferred

Tools

Epic Systems
Microsoft Office

Job description

Hospital for Special Surgery seeks a Clinical Research Coordinator to join the Arthroplasty Service research team. The role supports day-to-day research activities, patient coordination, and data management ensuring efficient operations and regulatory compliance.

The coordinator will work under the Arthroplasty Director, participate in protocol development, and assist with enrollment, data collection, and IRB documentation while supporting other research staff in a collaborative setting.

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