Clinical Research Coordinator I – CHPS Nutrition and Growth Lab

Found in: Talent US C2 - 2 weeks ago


Philadelphia, United States The Children’s Hospital of Philadelphia Full time
JOB DESCRIPTION

SHIFT:

Day (United States of America)

The Clinical Research Coordinator I for NGL provides testing of research participants on 1) growth (using various hands-on anthropometric measurements); 2) tests for body composition; 3) scans for bone health (DXA, peripheral
quantitative computed tomography); 4) tests to measure muscle strength: and 4) energy expenditure. In addition to data acquisition, the Clinical Research Coordinator I will assist with data analysis and coordinating lab scheduling. NGL provides a comprehensive training and certification program on all equipment and measures used in the NGL.

Under the supervision of the Administrative Manager and the Director of the CHPS NGL, the Clinical Research Coordinator I works with the NGL team to coordinate and complete clinical research activities within the scope of
clinical research protocols, interacting and communicating with patients, families and other research staff for study visit completion.

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
• Report adverse events
• Understandgood 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 Related responsibilities • Manage essential regulatory documents • Register study on ClinicalTrial.gov
• 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
• Facilitate study close out activities
• Coordinate research/project team meetings
• Collect, process and ship laboratory specimens
• Schedule subject visits and procedures
• Retain records/archive documents after study close out

Education Qualifications

High School Diploma / GED Required Bachelor's Degree Preferred Bachelor's Degree Biology, exercise physiology, or nutrition 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.

Employees may request exemptions for valid religious and medical reasons. Start dates may be delayed until candidates are immunized or exemption requests are reviewed.

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