Clinical Research Assistant I - Division of Emergency Medicine Part Time

Evening shift in the United States of America.

About the role

The Division of Emergency Medicine (DoEM) is seeking a part-time clinical research assistant who will join a highly productive research team focused on conducting a variety of research projects at our King of Prussia location. Researchers in CHOP's DoEM are national leaders in efforts to address important social, biological, and environmental determinants of health for children across the continuum of emergency care – from prevention to recovery.

Under the supervision of the Program Manager and the Associate Director of Research Operations, the research assistant responsibilities include coordinating clinical research activities within the scope of specific research protocols under the guidance of the study PI and Program Manager. The incumbent will assist with recruitment and enrollment of research participants, complete data entry, and follow up with participants as required by the study protocol. Other tasks may be assigned as needed.

Responsibilities

• Provide technical and administrative support in the conduct of clinical research:
  • Patient/research participant scheduling
  • Patient/Research Participant screening for inclusion/exclusion criteria or case history
  • Data collection
  • Data entry
  • Data management
  • Laboratory sample processing
  • Clinical research study procedures or questionnaire administration
  • Organization of research records and/or other study related documentation
• Research Study Compliance:
  • Adhere to IRB approved protocols and compliance with HIPAA and handling confidential materials
  • Comply with Institutional policies, SOPs and guidelines
  • Comply with federal, state, and sponsor policies
• Additional Responsibilities may include:
  • Consent subjects, with appropriate authorization and training
  • Document and report adverse events
  • Maintain study source documents
  • Complete case report forms (paper and electronic data capture)
  • Assist with IRB/regulatory submissions
  • Follow-up care
  • Order materials/supplies
  • Schedule research meetings

Requirements

• High School Diploma / GED Required
• Bachelor's Degree Preferred

Qualifications

• Previous relevant clinical research experience Required
• At least one (1) year of relevant clinical research experience Preferred

Skills

• Familiarity with IRB and human subject protection

Pay

$21.05 - $26.35 hourly. Salary ranges are shown for full-time jobs. If you're working part-time, your pay will be adjusted accordingly.