Clinical Research Assistant II -Neurosurgery & the Center for Data Driven Discovery

Children’s Hospital of Philadelphia•Philadelphia, PA

5d•$23 - $28

About The Position

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. A Brief Overview Under the direct supervision of the Principal Investigator and/or other study team members, this role provides experienced 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.

Requirements

High School Diploma / GED Required
At least one (1) year of relevant clinical research experience Required
Basic knowledge of IRB and human subject protection.

Nice To Haves

Bachelor's Degree Preferred
At least two (2) years of relevant clinical research experience Preferred

Responsibilities

Collects and delivers intraoperative specimens to pathology and research laboratories, ensuring accurate documentation and compliance with regulatory standards
Participate in the informed consent process for study subjects
Maintain study source documents
Filing and office organization
Data collection/extraction from EPIC (electronic medical record system) and entry into project databases and platforms
Data management, including assisting with quality control and data review
Assist with the redaction of pathology, operative, or MRI reports
Schedule research meetings and rooms when needed
Comply with Institutional policies, study SOPs and guidelines
Must comply with federal, state, and sponsor policies
Submit basic IRB reports
Must possess knowledge of IRB and human subject protection and must adhere to an IRB approved protocol (through Citi Program Certification performed following hiring)
Other tasks as assigned
Patient/research participant scheduling
Patient/research participant history
Laboratory procedures
Research Study Compliance
Adhere to IRB approved protocols and compliance with HIPAA and handling confidential materials
Support the safety of clinical research patients/research participants
Document and report adverse events
Assist with IRB/regulatory submissions
Complete case report forms (paper and electronic data capture)
Follow-up care
Order materials/supplies