Clinical Research Assistant II-Cellular Therapy and Transplant Section

A Brief Overview

The CHOP Cellular Therapy and Transplant Section (CTTS) is seeking candidates with relevant experience to join its Clinical Research Team.This is an exciting area of growth in CTTS @ CHOP which is one of the most active pediatric cell therapy programs in the world.

The successful candidate will be joining a team that implements outstanding cutting edge clinical, translational and outcomes research while providing outstanding clinical care to the patients we serve. Areas of research include CAR-T, and other cell and gene therapies.Your work will directly impact how we treat children with various cancers and other devastating diseases!

The Cellular Therapy Clinical Research Assistant II serves in a supportive role and interacts professionally with our clinical teams and directly with patients and families seeking Oncology services at The Children's Hospital of Philadelphia. Under supervision of the principal investigator and primary clinical research coordinate, they will manageand perform various aspects of clinical research activities within the scope of clinical research protocols.

We offer a unique and exciting multi-disciplinary environment in which to work. You can learn more about CTTS at: https://www.chop.edu/centers-programs/cellular-therapy-and-transplant-section.

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

• 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: Experience in REDCap and EPIC

Skills and Abilities

• Basic knowledge of IRB and human subject protection