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Clinical Research Coordinator I - Nephrology
Location:
Philadelphia, PA
Description:
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 The Division of Nephrology at the Children's Hospital of Philadelphia conducts many research studies to understand kidney disease, advance current treatments, improve quality of life, and develop new therapies. We are seeking an enthusiastic individual to join our research team as a Clinical Research Coordinator. The coordinator will primarily work on the IMPAKT study, Imaging Modalities in Pediatric Assessment of Kidney Transplants, led by Dr. Bernarda Viteri. In this study, we are developing new magnetic resonance imaging (MRI) and ultrasound methods to determine if it is effective in diagnosing complication in kidney transplant patients. The project is funded by the National Institutes of Health. The candidate for this position will play a critical role in implementing study protocols, recruiting participants, scheduling in-person study visits, and assisting with data management. An ideal candidate is highly organized, diligent, has strong communication and management skills, empathetic to patients and families, and has experience working in clinical research. The candidate may also assist with other ongoing projects in the Division or with new projects that are initiated after their start date. What you will do Core responsibilities 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 Under the supervision of PI Report adverse events 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, and with HIPAA and management of confidential materials Must comply with federal, state, and sponsor policies For multi-site studies or collaborations, support communication and meeting scheduling across teams Related responsibilities Manage essential regulatory documents Register study on ClinicalTrials.gov as appropriate Complete case report forms (paper & 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) Facilitate pre-study, site qualification, study initiation, and monitoring visit as appropriate Facilitate study close out activities as appropriate Coordinate research/project team meetings Collect, process and ship samples as applicable to the protocol Schedule subject visits and procedures Retain records/archive documents after study close out Education Qualifications High School Diploma / GED Required Bachelor's Degree Preferred Experience Qualifications At least two (2) years of clinical or clinical related or research related experience Required At least three (3) years of clinical or clinical related or research related experience Preferred Skills and Abilities Basic knowledge of IRB and human subject protection Strong verbal and written communications skills Strong time management 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 be fully vaccinated against COVID-19 and receive an annual influenza vaccine. Learn more. 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
Company:
Children's Hospital Of Philadelphia
Industry:
Other
Posted:
March 24 on Professional Diversity Network
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More About this Listing: Clinical Research Coordinator I - Nephrology
Clinical Research Coordinator I - Nephrology is a Nurse & Healthcare Clinical Coordinator, Clinical Research Coordinator, Research Associate Job at Children's Hospital of Philadelphia located in Philadelphia PA. Find other listings like Clinical Research Coordinator I - Nephrology by searching Oodle for Nurse & Healthcare Clinical Coordinator, Clinical Research Coordinator, Research Associate Jobs.
Clinical Research Coordinator I - Nephrology is a Nurse & Healthcare Clinical Coordinator, Clinical Research Coordinator, Research Associate Job at Children's Hospital of Philadelphia located in Philadelphia PA. Find other listings like Clinical Research Coordinator I - Nephrology by searching Oodle for Nurse & Healthcare Clinical Coordinator, Clinical Research Coordinator, Research Associate Jobs.