Full-Time Clinical Research Coordinator I
Job Description
Philadelphia, PA, US, 19104
Location: LOC_ROBERTS-Roberts Ctr Pediatric Research
Req ID: 97659
Shift: Any
Employment Status: Regular – Full Time
Job Summary
This is a full time Clinical Research Coordinator (CRC) position offered through PolicyLab and the Division of General Pediatrics at Children’s Hospital of Philadelphia. The CRC will assist the Principal Investigator in activities related to PriCARE and CAPNET. Under minimal supervision, the CRC will facilitate all clinical research activities within the scope of the clinical research protocols. The CRC will also be responsible for training and overseeing more junior staff and research assistants. The ideal candidate will possess at least 2 years of related research experience.
PriCARE is a group parent training program for caregivers of children ages 2-6 who have some behavioral problems. The program aims to strengthen parent-child relationships and improve the children’s behaviors. To support the implementation of this intervention and research study, the ideal candidate will have some flexibility of hours, experience working with diverse, low-income families, experience with research study management, and excellent interpersonal skills.
Child Abuse Pediatrics Research Network (CAPNET) is a multi-site research collaborative that was established to facilitate robust, multi-center research focused on the diagnosis, treatment, and prevention of child physical abuse. The ideal candidate will have experience in REDCap data collection, entry, maintenance, and analysis.
Link for PriCARE: https://www.chop.edu/centers-programs/pricare-parenting-program
Link for CAPNET: https://policylab.chop.edu/project/capnet-improving-child-abuse-care-and-outcomes-through-multi-center-research
Job Responsibilities
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
- 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
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
How to Apply
https://careers.chop.edu/job/Philadelphia-Clin-Research-Coordinator-I-65002-PA-19104/731449900/162 total views, 0 today