Clinical Research Coordinator III - PEDSnet

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A Brief Overview

PEDSnet is seeking a highly motivated Clinical Research Coordinator III who will join an internationally recognized group at the Children's Hospital of Philadelphia working to transform the health of children. He or she will work within a dynamic team of researchers, data scientists, and programmers, as part of PEDSnet (https://www.pedsnet.org), and the Research Institute's Applied Clinical Research Center (ACRC), to understand predictors of childhood diseases, improve the quality of children's healthcare, and rapidly advance knowledge through the creation and development of learning health systems.

The Clinical Research Coordinator III will apply in-depth knowledge of clinical research and independently coordinate the activities of one or more large-scale, complex multi-center/multi-institutional studies within the PEDSnet network. The Coordinator will be responsible for managing and coordinating individual PEDSnet research projects-working with study teams to create and monitor project timelines, ensuring all regulatory and contractual agreements are in place, ensuring all project deliverables are met, and updating project status and tasks in the PEDSnet project management system. The Coordinator will be accountable for study oversight at one or more sites/institutions and will provide oversight in the preparation, management, and monitoring of study budgets.

The Coordinator will provide critical support for PEDSnet Operations and Governance work, including organizing meetings and providing administrative support for PEDSnet Committee and Workgroup meetings. Responsibilities include managing PEDSnet IRB and other regulatory approvals, preparing grant documents and letters of support, tracking and creating reports on project deliverables and metrics, and providing general support to the PEDSnet PIs as needed.

The Coordinator will collaborate internal and external clinical staff, research teams, and other coordinators, providing resources and consulting on difficult protocols or projects. Independent of the PI, the Coordinator will assess and critique protocol feasibility and provide recommendations to improve study design and implementation. As a front-facing representative of PEDSnet, the Coordinator plays a critical role in external engagement and relationship management, managing communications, coordinating data access requests, and managing account access for PEDSnet collaborators across multiple institutions.

Must be able to maintain confidentiality of information, meet deadlines, work on several projects simultaneously, and work independently while understanding the goals and concepts involved in the work performed. Must be able to establish and maintain a shared work environment and consistently achieve open, effective communication with staff within the Center and across participating PEDSnet sites.

What you will do

• Applies in depth knowledge of clinical research and independently coordinates the activities of 1 or more large-scale, complex multi-center / multi-institutional studies
• Provides oversight in the preparation, management and monitoring of study budgets
• Accountable for study oversight at one or more sites/institutions
• May be responsible for conducting monitoring activities at one or more sites/institutions
• Prepares study sites for internal/external regulatory audits (sponsor, FDA, NIH, etc)
• Facilitates and/or leads research/projectteammeetings
• Educates and mentors internal and external clinical staff, research teams and other coordinators; provides resources, and consulting on difficult protocols or projects
• Independent of the PI assesses and critiques protocol feasibility and provides recommendations
• May support 1 or more PI sponsored INDs or IDEs
• Liaises between Research billing (CTFM) and the research team
• Participate in the informed consent process of study subjects
• Scheduling, facilitating and/or leading research/project team meetings
• Screen, recruit and enroll patients/research participants
• Report adverse events
• Comply with Institutional policies, standard operating procedures (SOPs) and guidelines
• Must comply with federal, state, and sponsor policies

Education Qualifications

• Bachelor's Degree Required
• Master's Degree in a related field Preferred

Experience Qualifications

• At least four (4) years of clinical/research coordination experience Required
• At least five (5) years of clinical/research coordination experience Preferred

Skills and Abilities

• Intermediate knowledge of IRB and human subject protection
• Basic proficiency in data management systems/tools
• Excellent verbal and written communications skills
• Excellent time management skills
• Solid analytical skills
• Ability to collaborate with stakeholders at all levels

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.

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SALARY RANGE:

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

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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. Click here for more information regarding CHOP's Compensation and Benefits.