Full-Time Clinical Research Coordinator I – Pediatric IDEAS Research Group
Job Description
Philadelphia, PA, US, 19146
Location: LOC_ROBERTS-Roberts Ctr Pediatric Research
Req ID: 117441
Shift: Days
Employment Status: Regular – Full Time
Job Summary
The successful candidate will join the research team of Dr. Jeffrey Gerber in the Pediatric IDEAS Research Group at Children’s Hospital of Philadelphia. Dr. Gerber’s research focuses on the epidemiology and outcomes of antimicrobial use in children with the goal of improving clinical outcomes while limiting the emergence of antimicrobial resistance. His approach benchmarks antimicrobial use across clinical settings to identify high-impact targets for improvement, followed by 1) comparative effectiveness studies for clinical scenarios where practice variability exists in the absence of evidence; 2) interventions to implement and disseminate evidence- based practice where prescribing guidelines do exist; and 3) qualitative assessments of the clinician, practice, or institution-level factors that might drive antimicrobial prescribing.
The candidate will be a member of the Pediatric IDEAS Research Group, a collaborative group of investigators within the Center for Pediatric Clinical Effectiveness (CPCE) at CHOP. The mission of the Pediatric IDEAS Research Group is to perform rigorous clinical and translational research that generates evidence on the prevention and treatment of infections to inform best practices and improve the health of children, families, and communities.
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
Required Licenses, Certifications, Registrations
Required Education and Experience
Required Education:
- Associates Degree or active enrollment in a Bachelor’s Degree Program
Required Experience:
- Three (3) years of coordination related, clinical related or research related experience.
How to Apply
https://careers.chop.edu/job/Philadelphia-Clinical-Research-Coordinator-I-Pediatric-IDEAS-Research-Group-PA-19146/745242800/?locale=en_US173 total views, 0 today