Clinical Research Assistant II

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 does not discriminate on the basis of race, color, sex, national origin, religion, or any other legally protected categories in any employment, training, or vendor decisions or programs. CHOP recognizes the critical importance of a workforce rich in varied backgrounds and experiences and engages in ongoing efforts to achieve that through equally varied and non-discriminatory means.

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.

• Providing technical and clinical support in the conduct of clinical studies
• Filing and office organization
• Patient/research participant scheduling
• Patient/research participant history
• Data collection/extraction from electronic medical record systems and entry into project databases and platforms
• Data management, including assisting with quality control and data review
• 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
• Comply with Institutional policies, SOPs and guidelines
• Comply with federal, state, and sponsor policies
• Additional Responsibilities may include
• Participate in the informed consent process for study subjects
• Document and report adverse events
• Maintain study source documents
• Submit basic IRB reports
• Assist with IRB/regulatory submissions
• Complete case report forms (paper and electronic data capture)
• Follow-up care
• Order materials/supplies
• Schedule research meetings

• High School Diploma / GED Required
• Bachelor's Degree Preferred

• At least one (1) year of relevant clinical research experience Required
• At least two (2) years of relevant clinical research experience Preferred

• Basic knowledge of IRB and human subject protection.

To carry out its mission, CHOP is committed to supporting the health of our patients, families, workforce, and global community. As a condition of employment, CHOP employees who work in patient care buildings or who have patient facing responsibilities must receive an annual influenza vaccine. Learn more. EEO / VEVRAA Federal Contractor | Tobacco Statement

$22.61 - $28.26 Hourly

Salary ranges are shown for full-time jobs. If you're working part-time, your pay will be adjusted accordingly.

At CHOP, we are committed to fair and transparent pay practices. Factors such as skills and experience could result in an offer above the salary range noted in this job posting.  for more information regarding CHOP's Compensation and Benefits.