Clinical Research Assistant I (Bilingual/Spanish Speaking) - Center for Autism Research (CAR)

Children's Hospital of Philadelphia • Philadelphia, PA

87d

About The Position

The Center for Autism Research (CAR) is conducting a wide range of studies seeking to understand autism spectrum disorder and to explore effective interventions and other supports for families throughout the region who have a family member with an autism diagnosis. Working at CAR provides the opportunity to be a part of innovative, breakthrough research on this complex developmental condition that affects 1 in 31 people in the United States. Most studies at CAR involve behavioral evaluations, brain imaging, and/or genetics aimed at identifying the fundamental mechanisms of ASD. We are seeking a full-time bilingual Spanish-speaking Clinical Research Assistant I (CRA I) to collaborate on different projects at CAR, including social and emotional development, non-social features of autism, supporting the transition to adulthood, clinical trials, and the relationship of motor and social development among youth with and without an autism diagnosis.

Requirements

• High School Diploma / GED - Required
• Previous relevant clinical research experience - Required
• At least one (1) year of relevant clinical research experience - Preferred
• Experience with project coordination and oversight of volunteers or undergrad students a plus
• Experience working with children and adolescents with an autism spectrum disorder or other developmental disorder and their families is preferred
• Statistical knowledge and interest; ability to use/learn a statistical software package (e.g., SPSS, R) is preferred
• Computer skills including Word, Excel, stimulus presentation software (e.g., python, MATLAB), and database software are preferred

Nice To Haves

• Bachelor's degree in psychology, child development, pre-med, or similar, with some prior 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
• Follow-up care
• Order materials/supplies
• Schedule research meetings

Benefits

• Diversity, Equity, and Inclusion commitment
• Opportunity to work in a collaborative environment
• Support for professional development

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Industry: Hospitals
• Education Level: High school or GED
• Number of Employees: 5,001-10,000 employees