Children's Hospital of Philadelphia

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 diverse talent who can help us deliver on our mission to be a world leader in the advancement of healthcare for children.

We strongly encourage all candidates of diverse backgrounds and lived experiences to apply.

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.

What you will do

• 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

Education Qualifications

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

Experience Qualifications

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

Skills and Abilities

• Basic knowledge of IRB and human subject protection. (Required proficiency)

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 be fully vaccinated against COVID-19 and receive an annual influenza vaccine. Learn more.

Employees may request exemptions for valid religious and medical reasons. Start dates may be delayed until candidates are immunized or exemption requests are reviewed.

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