Clinical Research Assistant I - Center for Autism Research
Children's Hospital of PhiladelphiaAbout the role
SHIFT:
Day (United States of America)Seeking Breakthrough Makers
Children’s Hospital of Philadelphia (CHOP) offers countless ways to change lives. Our diverse community of more than 20,000 Breakthrough Makers will inspire you to pursue passions, develop expertise, and drive innovation.
At CHOP, your experience is valued; your voice is heard; and your contributions make a difference for patients and families. Join us as we build on our promise to advance pediatric care—and your career.
CHOP’s Commitment to Diversity, Equity, and Inclusion
CHOP is committed to building an inclusive culture where employees feel a sense of belonging, connection, and community within their workplace. We are a team dedicated to fostering an environment that allows for all to be their authentic selves. We are focused on attracting, cultivating, and retaining talent who can help us deliver on our mission to be a world leader in the advancement of healthcare for children. We strongly encourage candidates of all races, colors, ethnicities, religions, perspectives, sexes, backgrounds, and lived experiences to apply.
A Brief Overview
The Center for Autism Research (CAR) is conducting a wide range of studies seeking to identify the causes of autism spectrum disorder (ASD), and to explore effective interventions and other supports for families throughout the region who are affected by ASD. Working at CAR provides the opportunity to be a part of innovative, break-through research on a complex developmental disorder that affects 1 in 31 people in the United States. Most studies at CAR involve behavioral evaluations, brain imaging, and genetics aimed at explaining the underlying mechanisms of this complex disorder.
We are seeking a full-time Clinical Research Assistant I (CRA I) to collaborate on a number of clinical research studies at CAR that include (but are not limited to) innovative interventions and/or clinical trials for ASD, language and motor development, and genetic disorders associated with ASD. The ideal candidate is highly organized, has excellent people skills, is self-motivated and curious, and possesses an analytical mind. Project coordination will be a key part of this position, requiring the CRA to organize workflows, guide work-study students, monitor multiple tasks simultaneously, and support progress reports.
CRA duties may include but will not be limited to: assisting in all aspects of participant recruitment, including contacting parents and teachers to obtain their consent, scheduling visits and data collection calls, distributing consent forms, and maintaining accurate records; collecting data on preschool, school-age children, adolescents and adults through various study paradigms in the lab or in homes (videotaping/audiotaping activities, one-on-one testing of children) and administering phone-based standardized screenings or tests; organizing data collected through paper and pencil or online questionnaires and tests, compiling and reducing large quantities of data under the direction of the principal investigator; performing data entry, coding and analysis, entering testing data into databases and/or spreadsheets, assisting with statistical analysis of data using statistical software and Excel; supporting work-study students; assisting with IRB protocol amendments, poster presentations, and assisting with publication preparation (including conducting literature reviews, creating figures, etc.); coordinating with collaborating research groups.
The CRA will work as part of a team composed of developmental psychologists, clinical psychologists, physicians, and computer scientists. CAR is a collaborative environment; we are looking for a self-motivated team player with excellent problem-solving and interpersonal skills to support our research efforts. Prior experience with some or all of these duties is a plus but is not necessary; many Research Assistant duties can be learned on the job. Successful applicants will be fast learners who enjoy working in a bustling research environment.
What you will do
- 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
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