Stony Brook University - Stony Brook, NY

posted 7 days ago

Full-time
Stony Brook, NY
Educational Services

About the position

The Clinical Research Assistant will play a crucial role in supporting the coordination of various clinical research trials, ensuring compliance with federal guidelines and assisting with the enrollment and data collection processes. This position involves interaction with multiple stakeholders, including sponsors and regulatory agencies, and requires a strong understanding of clinical research protocols and administrative duties.

Responsibilities

  • Assist RN/CRA in coordinating various research trials and ensure compliance with federal guidelines.
  • Interact and correspond with internal and external constituents including sponsors, cooperative groups, Institutional Review Board, and regulatory agencies.
  • Assist with enrolling, registering, and screening patients for clinical research trials.
  • Collect and submit clinical trial patient data.
  • Perform various administrative duties, including proper collection and shipment of lab samples, billing and budgeting, and maintenance of clinical research study supplies and drug accountability.
  • Maintain research databases and assist with clinical trial enrollment reconciliation.
  • May assist with coordinating the work of other staff.
  • Other duties as assigned.

Requirements

  • Associate's degree (foreign equivalent or higher).
  • Experience working on clinical research projects.
  • Experience with the screening and/or enrollment of study participants.
  • Experience with collecting and entering research data and/or data analysis.

Nice-to-haves

  • Bachelor's degree (foreign equivalent or higher).
  • Clinical trial experience with interventional cardiology.
  • Completion of the Collaborative Institutional Training Initiative (CITI).
  • Group 2B Biomedical Researcher certification.
  • Good Clinical Practice (GCP) and Conflict of Interest (COI) training.
  • Experience with database maintenance.
  • Proficiency with MS Office (Word, Excel, and PowerPoint).
  • Experience working with medical terminology.
  • Experience in assisting with IRB paperwork.

Benefits

  • Eligible for overtime provisions of the FLSA.
  • Diversity and inclusion initiatives.
  • Disability-related accommodations available.
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