Research Coordinator I

Posted 16 Days Ago
Be an Early Applicant
Los Angeles, CA, USA
In-Office
32-42 Hourly
Junior
Edtech
The Role
Coordinates clinical trials and observational research in Alzheimer’s disease and related disorders. Responsibilities include participant recruitment and scheduling, clinical assessments, data collection and analysis, regulatory documentation, informed consent, study monitoring, audit readiness, sponsor visits, reporting, and research team guidance. The role requires maintaining protocol compliance and high-quality documentation while supporting operational and regulatory improvements.
Summary Generated by Built In

The Department of Psychiatry and Behavioral Sciences at the Keck School of Medicine of USC is seeking a detail-oriented and highly motivated Research Coordinator I to support clinical trials and observational research in Alzheimer's disease, related dementias, and neurodegenerative disorders.

Working directly under the supervision of Dr. Lon Schneider, Professor of Psychiatry, Neurology, and Gerontology, the Research Coordinator I will support the day-to-day coordination of study activities, including participant recruitment, regulatory documentation, and data management. The successful candidate will be able to work independently on assigned responsibilities, maintain high-quality study documentation, support ongoing monitoring, and audit readiness, and contribute to improved regulatory and operational processes across the research program.

Essential job duties include, but are not limited to:

  • Coordinate assessments, tests, and other assigned clinical trial activities to meet research objectives and study protocol compliance.
  • Support participant recruitment, screening, eligibility tracking, orientation, scheduling, and correspondence.
  • Collect, record, manage, and analyze data for research studies. 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 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. The University reserves the right to add or change duties at any time. 

Required Qualifications:

  • Bachelor’s degree (in life sciences, health sciences, pharmacy, psychology, neuroscience, public health, regulatory science, clinical research, or a related field) or equivalent combination of education and experience.
  • Minimum one-year of administrative or research experience.
  • Proficiency with MS Office applications
  • Excellent written and oral communication skills
  • Strong attention to detail
  • Ability to multi-task and prioritize.
  • Demonstrated ability to work independently and collaboratively.

Preferred Qualifications:

  • 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 medical environment and terminology
  • Familiarity with USC systems and workflows, including OnCore, IRB submissions, REDCap, SharePoint, sponsor portals, and other Electronic Data Capture (EDC) systems and Clinical Trial Management Systems (CTMS).

Work Location

This position is full-time on-site and employee must report to work at the USC Health Science Campus in Los Angeles, CA when scheduled. Work hours and on-site days may be subject to change depending on business needs.

The hourly rate range for this position is $32.45 - $42.48. When extending an offer of employment, the University of Southern California considers factors such as (but not limited to) the scope and responsibilities of the position, the candidate's work experience, education/training, key skills, internal peer equity, federal, state and local laws, contractual stipulations, grant funding, as well as external market and organizational considerations.

Minimum Education: Bachelor's degree, Combined experience/education as substitute for minimum education
Minimum Experience: 1 year
Minimum Field of Expertise: Administrative or research experience. Working knowledge of MS Office applications. Demonstrated effective communication and writing skills. Ability to multi-task and prioritize. Demonstrated ability to work as part of a team as well as independently.

                                                  

USC is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other characteristic protected by law or USC policy. USC observes affirmative action obligations consistent with state and federal law. USC will consider for employment all qualified applicants with criminal records in a manner consistent with applicable laws and regulations, including the Los Angeles County Fair Chance Ordinance for employers and the Fair Chance Initiative for Hiring Ordinance, and with due consideration for patient and student safety. Please refer to the Background Screening Policy Appendix D for specific employment screen implications for the position for which you are applying. 

We provide reasonable accommodations to applicants and employees with disabilities. Applicants with questions about access or requiring a reasonable accommodation for any part of the application or hiring process should contact USC Human Resources by phone at (213) 821-8100, or by email at [email protected]. Inquiries will be treated as confidential to the extent permitted by law.

  • Notice of Non-discrimination
  • Employment Equity
  • Read USC’s Clery Act Annual Security Report
  • USC is a smoke-free environment
  • Digital Accessibility

                                                  

If you are a current USC employee, please apply to this  USC job posting in Workday by copying and pasting this link into your browser:

https://wd5.myworkday.com/usc/d/inst/1$9925/9925$152349.htmld

Skills Required

  • Bachelor's degree in life sciences, health sciences, pharmacy, psychology, neuroscience, public health, regulatory science, clinical research, or a related field, or equivalent education and experience
  • At least one year of administrative or research experience
  • Proficiency with Microsoft Office applications
  • Excellent written and oral communication skills
  • Strong attention to detail
  • Ability to multitask and prioritize
  • Ability to work independently and collaboratively
  • 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 a medical environment and terminology
  • Familiarity with USC systems and workflows, including OnCore, IRB submissions, REDCap, SharePoint, sponsor portals, EDC systems, and CTMS platforms
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