Pediatric GI Clinical Research Assistant — Data-Driven Impact

Children's Hospital of Philadelphia; Alaska; On-site; USD 8,300 - 25,000; Full time

Job summary

Children's Hospital of Philadelphia (CHOP) seeks a GI Clinical Research Assistant to support pediatric studies. You will assist in subject recruitment, confirm eligibility, obtain informed consent, and help with case report forms and data clarification across studies.

You will maintain regulatory documents, prepare materials for IRB approvals, and collaborate with teams to ensure protocol compliance, data integrity, and timely study reporting. Prior research exposure is preferred.

Qualifications

• High School Diploma or GED required; enrollment in school acceptable.
• Bachelor's degree preferred.
• Internships or paid experiences coordinating research activities varying size and complexity required/preferred (as applicable).

Responsibilities

• Adheres to recruitment/enrollment strategies
• Maintains regulatory documents per the established protocol or sponsor requirements
• Creates/reviews source documents and sets up study files
• Ensure compliance with protocol guidelines and requirements of regulatory agencies
• Analyzes data through the use of memos, coding and qualitative analytic software
• Assist in the preparation of reports and professional research papers
• Assist in preparation of materials to submit for IRB approval
• Renders age appropriate care & services based on the patient and/or their developmental needs

Skills

Written communication

Organizational skills

Attention to detail

Teamwork

GCP training

IRB knowledge

Age-appropriate care

Education

High School Diploma / GED

Bachelor's degree

Tools

Microsoft Office

Job description

Children's Hospital of Philadelphia (CHOP) seeks a GI Clinical Research Assistant to support pediatric studies. You will assist in subject recruitment, confirm eligibility, obtain informed consent, and help with case report forms and data clarification across studies.

You will maintain regulatory documents, prepare materials for IRB approvals, and collaborate with teams to ensure protocol compliance, data integrity, and timely study reporting. Prior research exposure is preferred.