Clinical Research Assistant II - Division of Adolescent Medicine

A Brief Overview
Provide technical and clinical support as a Clinical Research Assistant at CHOP. Under the supervision of the study team, you'll coordinate details of the human research subject and document concerning protocols.

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.

Responsibilities

• Supports Adolescent Initiative [AI] research projects by:
• Recruiting participants for intervention sessions using social media and venue-based methods.
• Is trained in and delivers study intervention providing health coaching.
• Completes data collection and entry.
• Strategizes for participant retention.
• Attends protocol meetings as needed.
• Other AI research duties as assigned.
• Assist in participant scheduling, history intake, and follow-up care.
• Collect, enter, and manage data.
• Adhere to IRB-approved protocols, laboratory procedures, and institutional, federal, state, and sponsor policies.
• Complete administrative duties, including filing, organizing, ordering supplies, and scheduling meetings.
• Participate in the informed consent process for study subjects.
• Document and report adverse events.
• Maintain study source documents, submit IRB reports, and complete case report forms.

Education

• Required: Associate degree

• Preferred: Bachelor's degree

Experience

• Required: At least two (2) years relevant clinical research experience

• Preferred: Previous experience in community-based work

Skills and Abilities

• Basic knowledge of IRB and human subject protection