What are the responsibilities and job description for the Clinical Research Coordinator - GI Nutrition position at Children's Hospital of Philadelphia?
SHIFT:
Day (United States of America)
Clinical Research Coordinator III
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
This study aims to define the composition of the human virome (the viruses that inhabit the human body) in early life. The human virome is vast, differs among human individuals, and changes over the lifespan. This study will enroll children who previously participated in a birth cohort study at CHOP and follow them longitudinally over three years.
This role functions independently in a clinical research setting and is responsible for the complete coordination of assigned clinical research activities within the scope of clinical research protocols. May have supervisory responsibilities of study team staff.
What You Will Do
Employees may request exemptions for valid religious and medical reasons. Start dates may be delayed until candidates are immunized or exemption requests are reviewed.
EEO / VEVRAA Federal Contractor | Tobacco Statement
Day (United States of America)
Clinical Research Coordinator III
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
This study aims to define the composition of the human virome (the viruses that inhabit the human body) in early life. The human virome is vast, differs among human individuals, and changes over the lifespan. This study will enroll children who previously participated in a birth cohort study at CHOP and follow them longitudinally over three years.
This role functions independently in a clinical research setting and is responsible for the complete coordination of assigned clinical research activities within the scope of clinical research protocols. May have supervisory responsibilities of study team staff.
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/project team meetings
- 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
- Bachelor's Degree Required
- Master's Degree in a related field Preferred
- At least four (4) years of clinical/research coordination experience Required
- At least five (5) years of clinical/research coordination experience Preferred
- 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
Employees may request exemptions for valid religious and medical reasons. Start dates may be delayed until candidates are immunized or exemption requests are reviewed.
EEO / VEVRAA Federal Contractor | Tobacco Statement
