U

University of Southern California

Research university in Los Angeles, CA

Research Coordinator 1

Full-Time
$32.45 - $42.48/hr
Junior
Bachelor's, Master's
Los Angeles, CA, USA
In Person
Biology & BiotechClinical Research Operations

About the job

Requirements
  • A bachelor's degree in life sciences, health sciences, pharmacy, psychology, neuroscience, public health, regulatory science, clinical research, or a related field, or an equivalent combination of education and experience.
  • At least one year of administrative or research experience.
  • Proficiency with Microsoft Office applications.
  • Strong attention to detail and ability to multitask and prioritize.
  • Ability to work independently and collaboratively.
Responsibilities
  • Coordinate assessments, tests, and other assigned clinical trial activities to meet research objectives and comply with study protocols.
  • Support participant recruitment, screening, eligibility tracking, orientation, scheduling, and correspondence.
  • Collect, record, manage, and analyze research data; prepare and submit accurate, complete, and timely reports according to project schedules or on an ad hoc basis.
  • Maintain regulatory documentation, including submissions, amendments, and informed consent, in compliance with FDA, GCP, IRB, HIPAA, SOPs, sponsor policies, and institutional policies.
  • Prepare sites for sponsor monitor visits and internal reviews, quality assurance checks, and audit-readiness activities.
  • Organize project-related meetings and events to increase knowledge about clinical trials and regulations.
  • Provide ongoing guidance to research personnel and study participants to maintain compliance.
  • Perform other related duties as assigned or requested.
Desired Qualifications
  • A master's degree or two or more years of relevant experience.
  • Experience in Alzheimer's disease, dementia, neurodegenerative disease, neurology, psychiatry, geriatrics, or CNS clinical trials.
  • Experience coordinating research activities, including clinical trials and human subjects research.
  • Knowledge of the medical environment and terminology.
  • Familiarity with USC systems and workflows, including OnCore, IRB submissions, REDCap, SharePoint, sponsor portals, other Electronic Data Capture (EDC) systems, and Clinical Trial Management Systems (CTMS).

About the company

U

University of Southern California

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The University of Southern California is a private research university with academic programs across the arts, sciences, business, engineering, law, health, and other professional fields.

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