Principal Clin Research Coord

Principal Clin Research Coord City of Hope - 3.6 Duarte, CA Job Details Full-time $44.90 - $69.60 an hour 10 hours ago Qualifications EMR/EHR Clinical research compliance Bachelor's degree Research regulatory compliance IRB compliance FDA regulations Full Job Description Join the transformative team at City of Hope, where we're changing lives and making a real difference in the fight against cancer, diabetes, and other life-threatening illnesses. City of Hope's growing national system includes its Los Angeles campus, a network of clinical care locations across Southern California, a new cancer center in Orange County, California, and treatment facilities in Atlanta, Chicago and Phoenix. Our dedicated and compassionate employees are driven by a common mission: To deliver the cures of tomorrow to the people who need them today. The System Clinical Trial Office (SCTO) supports COH investigators in managing human-subjects research by coordinating multi-phase clinical studies under the direction of SCTO leadership, Disease/Modality Team Chairs, and Study Investigators. Principal Clinical Research Coordinators/Clinical Trial Portfolio Leads (CTPLs) serve as leads within their disease teams, mentoring staff, providing guidance to Clinical Trial Data Coordinators, and acting as subject matter experts while ensuring strict compliance with research protocols, GCP, FDA, NIH, HIPAA, and institutional policies. CTPLs manage complex portfolios of approximately 30-50 oncology trials, oversee administrative and operational execution, support regulatory compliance and patient safety, and ensure studies meet quality, timeline, and resource expectations. They collaborate closely with managers, disease team leadership, and coordinators, maintain effective communication across teams, and function as Lead Central Coordinators and primary contacts for sponsors, investigators, national clinical trials, Hope Pathways, portfolio updates, and study-related inquiries. As a successful candidate, you will: Serves as the primary point of contact and liaison between study sponsors, investigators, and research teams, including managing Hope Pathways inquiries, eligibility criteria, and National Trial coordination. Oversees operational execution of studies, including patient registration, randomization, slot management, and study close-out activities, while supporting protocol implementation and troubleshooting issues. Ensures regulatory compliance and accurate documentation across systems (Florence, OnCore, iRIS, sponsor portals), including eRegulatory binders, study status updates, and required filings. Manages safety and sponsor reporting requirements, including AE/SAE collection, submission, and resolution of protocol deviations or unanticipated problems. Coordinates and participates in monitoring visits, audits, and inspections; addresses findings, communicates deadlines, prioritizes work, and contributes to process improvement initiatives. Qualifications - External Your qualifications should include:

Minimum Education:

• Bachelor's degree in science, Health or related field from an accredited university

Minimum Experience:

• Minimum of 5-7 years research or relevant experience Experience with CTMS, EMR and eRegulatory Systems Working knowledge of clinical trials, Federal, State, and Local regulations, and FDA/IRB regulations and requirements

Required Courses/Training:

Req.

Certification/Licensure:

• Good Clinical Practice (GCP) within 1 month of employment Human Subjects Protection (HSP) within 1 month of employment SOCRA or ACRP Certification within two years of employment City of Hope employees pay is based on the following criteria: work experience, qualifications, and work location. City of Hope is an equal opportunity employer. To learn more about our Comprehensive Benefits, please

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