Clinical Research Assistant - Center for Autism Research

Children's Hospital of PhiladelphiaPhiladelphia, PA
$21 - $26Onsite

About The Position

The Emotion and Neurodiversity Laboratory (ENL) led by Dr. John Herrington at the Center for Autism Research at the Children’s Hospital of Philadelphia studies the social and emotional experiences of neurodivergent youth. A central component of this position involves working on a new NIH grant focused on the identification facial expressions and other non-verbal behavior that can predict conversational success and satisfaction among autistic and non-autistic adolescents. Working at ENL provides the opportunity to collaborate with a wide range of collaborators to conduct innovative, breakthrough scientific research that improves the lives of stakeholders and families. We are seeking a full-time Clinical Research Assistant I (CRA I). A 2-year commitment is preferred. The CRA will organize data processing workflows, monitor undergraduate students, and support clinical study tasks simultaneously.

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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