Research Coordinator II

University of Southern CaliforniaLos Angeles, CA
Hybrid

About The Position

The Department of Population and Public Health Sciences is seeking a dependable, flexible, detail-oriented Research Coordinator II to join a research team at the University of Southern California. The Research Coordinator will support the implementation and day-to-day operations of several NIH-funded research grants. The position requires strong problem-solving skills, professionalism, and the ability to communicate effectively with diverse participant populations and research team members. USC is a leading private research university located in the heart of downtown Los Angeles – a global center for arts, technology and international business. As the largest private employer in the city – responsible for more than $5 billion annually in economic activity in the region – we offer the opportunity to work in a dynamic and diverse environment, in careers that span a broad spectrum of talents and skills. As a USC employee, you will enjoy excellent benefits and perks, and you will be a member of the Trojan Family - the faculty, staff, students and alumni who make USC a great place to work.

Requirements

  • Bachelor’s degree in a health-related or social science field
  • Minimum 2 years of administrative or research experience
  • Knowledge of medical environment and terminology
  • Knowledge and understanding of federal, state, and institutional research regulations as well as Good Clinical Practices (GCP) and HIPPA regulations
  • Proficient with MS Office applications
  • Demonstrated effective communication and writing skills
  • Ability to multi-task
  • Demonstrated ability to work as part of a team as well as independently
  • Strong organizational and interpersonal skills
  • Excellent attention to detail
  • Ability to work both independently and collaboratively while managing multiple competing priorities

Nice To Haves

  • Prior experience in a research environment
  • Staff education and orientation experience
  • Knowledge of Electronic Data Capture (EDC) systems and Clinical Trial Management Systems (CTMS)

Responsibilities

  • Coordinating study activities across multiple projects
  • Maintaining communication with study participants and scheduling research visits
  • Assisting with participant recruitment, screening, enrollment, and retention
  • Conducting interviews and administering questionnaires
  • Collecting and processing study data and biological specimens, as applicable
  • Entering and managing data in research databases
  • Ensuring compliance with study protocols and regulatory requirements
  • Providing overall project support to research staff and faculty investigators

Benefits

  • Excellent benefits and perks
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