Clinical Research Assistant 1 - The Division of Emergency Medicine

Children’s Hospital of PhiladelphiaPhiladelphia, PA
Onsite

About The Position

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 King of Prussia. 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 direct supervision of the Principal Investigator and/or other study team members, this role provides support in the conduct of clinical research. Job responsibilities may include human subject research activities including but not limited to subject enrollment, data/sample collection, data entry, and regulatory submissions support. This position will be for evening and weekend hours.

Requirements

  • High School Diploma / GED Required
  • Previous relevant clinical research experience Required
  • Familiarity with IRB and human subject protection.

Nice To Haves

  • Bachelor's Degree Preferred
  • At least one (1) year of relevant clinical research experience Preferred

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
  • 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
  • Complete case report forms or other study documentation (paper and electronic data capture)
  • Follow-up care
  • Order materials/supplies
  • Schedule research meetings

Benefits

  • Annual influenza vaccine
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