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CHA Hollywood Presbyterian Medical Center · 1 day ago

Associate Clinical Research Coordinator

United States-California-Duarte

Full-time

Onsite

Entry Level

$26.81/hr - $41.55/hr

1+ years exp

CHA Hollywood Presbyterian Medical Center is part of City of Hope, a transformative team dedicated to fighting cancer and other life-threatening illnesses. The Associate Clinical Research Coordinator will ensure the integrity of research studies, oversee laboratory kit readiness, coordinate biospecimen collection, and maintain updated patient data in the clinical research management system.

Health CareHospitalMedical

Responsibilities

Work under the supervision of the Manager, Study Investigators, and Senior Manager, with a focus on protocol-specific duties required by research protocols

Ensure adherence to protocol for specimen collection and sponsor-specific equipment procedures, guaranteeing accurate documentation

Identify and promptly communicate important protocol and data management issues to the supervisor

Uphold Good Clinical Practices, FDA Rules, NIH guidelines, HIPAA regulations, ICH guidelines, and institutional policies for clinical trials

Enter accurate and up-to-date data into the clinical research management system (CRMS) for study patients

Collaborate within the clinical research team, maintaining positive and effective communication while seeking ways to improve job performance and surroundings

Qualification

Oncology clinical trialsClinical trial managementClinical Practice (GCP)Clinical research management systemFederalState RegulationsCommunication skillsTeam collaborationAttention to detail

Required

Bachelor's degree. Experience may substitute for minimum education requirements. (Associate Degree plus minimum of 2 years of experience)

At least one year of experience related to the management and conduct of oncology clinical trials in an academic setting, or six months experience as a Project Coordinator or Biospecimen Coordinator in the CTO

Working knowledge of clinical trials, Federal, State, and Local Regulations, IRB requirements, consent form and protocol development

Good Clinical Practice (GCP) and Health Information Portability and Accountability ACT (HIPAA)-to be provided by COH if not already completed