Clinical Research Coordinator supporting pediatric research initiatives at Shriners Children's in Pasadena. Ensuring compliance with protocols and managing research data collection.
Responsibilities
Supports the implementation and conduct of approved research protocols
Performs study-specific research activities and/or interventions
Assists with participant recruitment, screening, informed consent/assent
Coordinates the collection and documentation of research data
Maintains regulatory documentation and study records
Supports communication between investigators, sponsors, monitors, and institutional departments
Assists investigators with the development and submission of research protocols
Contributes to study progress reports, monitoring visits, and audits
Requirements
Bachelor’s degree in Clinical Research, Life Sciences, Public Health, or another healthcare-related field
Working knowledge of regulations and guidance related to clinical research (e.g., GCP, FDA regulations, IRB requirements)
Experience coordinating intergroup or multi-site clinical studies
CCRP or CCRC certification
1 or more years of relevant research experience (e.g., study coordination, site management, regulatory submissions, or clinical data management)
Benefits
Medical coverage available on first day
403(b) Retirement Saving Plan with matching contributions of up to 6%
Clinical Research Fellow conducting clinical research in cardiothoracic surgery and cardiovascular disease at Emory University. This fellowship offers comprehensive training and mentorship in clinical research methodology.
Clinical Research Nurse providing nursing support for research trials at Emory University. Involves clinical patient contact and participation in research studies at School of Medicine.
Lead biostatistician consulting on clinical research studies at Winship Cancer Institute. Requires expertise in R, SAS, and statistical analysis with extensive experience.
Senior Principal Scientist managing clinical research activities involving investigational compounds in Immunology. Focusing on late - stage development and comprehensive clinical trial management.
Clinical Research Coordinator II coordinating research visits and participant eligibility for movement disorders and stroke studies. Involves regulatory compliance and data management.
Clinical Trial Manager overseeing global Phase 3 program for cardiovascular drug development. Responsible for regional study and vendor management while collaborating with clinical operations teams.
Clinical Research Nurse Supervisor leading coordination of clinical studies at the Perelman School of Medicine. Overseeing study conduct, compliance, and supervising clinical staff in a hybrid role.
Clinical Research Nurse coordinating complex clinical trials for RadOnc CRU at University of Pennsylvania. Responsible for patient care and collaboration with research team on clinical activities.
Clinical Research Coordinator managing complex clinical trials in the Neurosurgery department at University of Pennsylvania. Ensures compliance and promotes good clinical practice in research protocols with mentorship responsibilities.
Clinical Research Coordinator overseeing data collection and research tasks at University of Arkansas for Medical Sciences. Analyzing data and training staff in adherence to protocols and quality standards.