Clinical Research Coordinator I-Center for Data-Driven Discovery in Biomedicine

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

We are the Center for Data-Driven Discovery in Biomedicine (D3b - d3b.center), an ambitious and unique blend of experts in the field of pediatric brain tumor research. Our mission is to empower researchers to analyze biological and genomic data, so that they may discover insights that lead to cures or dramatically improved treatment options. We want creative problem solvers that are passionate about clinical research operations, biospecimen management and biobanking operations, and are excited to learn whatever is needed to empower our mission. As a Clinical Research Coordinator I, you will work with other study team members on project activities, primarily for consenting, clinical data management, biospecimen handling and accessioning, biospecimen data management, and quality control, for projects in our D3b portfolio.

What you will do

• Adhere to an IRB approved protocol

• Participate in the informed consent process of study subjects

• Support the safety of clinical research patients/research participants

• Coordinate protocol related research procedures, study visits, and follow-up care

• Screen, recruit and enroll patients/research participants

• Maintain study source documents

• Understand good clinical practice (GCP) and regulatory compliance

• Educate subjects and family on protocol, study intervention, etc.

• Comply with Institutional policies, standard operating procedures (SOPs) and guidelines

• Must comply with federal, state, and sponsor policies

• Manage essential regulatory documents

• Complete case report forms (electronic data capture) and address queries

• Submit documents to regulatory authorities (e.g. IRB, FDA, etc.) and/or review/monitoring boards (ie, DSMB, independent safety officer)

• Coordinate research/project team meetings

• Collect samples as applicable to the protocol such as saliva from subjects and relatives Schedule subject visits and procedures

• Retain records/archive documents after study close out

• Tracks biospecimens across platforms and performs biospecimen data entry

• Accessions biospecimens into a LIMS (Laboratory Information Management System) for integration into a biobank.

• Performs tasks that require familiarity with fundamental laboratory techniques and equipment, such as weighing tissue samples, evaluating specimens for deviations, handling biospecimens, and the storage of biospecimens

• Communicates with study collaborators about biobanking operations at CHOP and at external institutions

• Monitors supply levels at pathology and coordinates restocking supplies as needed

• Assists with planning specific research protocols and workflow optimization

• Provides required metrics for reports as needed

• Ensures all standard operating procedures and workflows are current and updated as needed

• Submits requests to the Biorepository Resource Center through iLab and coordinates execution of the requests

• Performs routine quality control on biospecimen inventory and data in the LIMS, specimen associations to patients in platforms, biospecimen documentation, and other biospecimen tracking

• Other biospecimen operational activities to support new research projects or initiatives as needed

Education Qualifications

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

Experience Qualifications

• At least two (2) years of clinical or research related experien