University of Southern California Logo

University of Southern California

Research Coordinator I

Posted 24 Days Ago
Be an Early Applicant
In-Office
Los Angeles, CA, USA
32-35 Hourly
Junior
In-Office
Los Angeles, CA, USA
32-35 Hourly
Junior
Coordinates daily clinical research activities in Cardiology under the supervision of the principal investigator and research leadership. Responsibilities include preparing IRB and regulatory submissions, organizing study files, screening and consenting participants, coordinating tests and registrations, collecting data, completing case report forms, maintaining supplies and records, communicating with sponsors and participants, supporting compliance reporting and ClinicalTrials.gov registration, assisting with study closeout, and coordinating participant payments.
The summary above was generated by AI

USC’s Keck School of Medicine, Department of Medicine, is seeking a  Research Coordinator I to join its Cardiology team. The Research Coordinator’s role is to support, facilitate and coordinate the daily activities of clinical research in Cardiology. The Research Coordinator works with and under the supervision of the Director of the Clinical Research Program and the clinical principal investigator (PI), as well as with the department, sponsor, and institution to assist with recruitment, data collection, IRB submission and other related aspects of clinical studies.

Specific job accountabilities will be:

General Administrative

  • Coordinates with Principal Investigator(s), department, and central administration to help ensure that clinical research and related activities are performed in accordance with Federal regulations and University and sponsoring agency policies and procedures.

Protocol Preparation & Review

  • Collaborates with the PI to prepare IRB and any other regulatory submission documents.
  • Prepares other study materials as requested by the PI. These study materials include, but are not limited to, informed consent documents, case report forms (CRFs), enrollment logs, and data collection forms.
  • Establishes and organizes study files, including but not limited to, regulatory binders, study specific source documentation and other materials.

Conduct of Research

  • Reviews and develops knowledge of the protocol, e.g. timelines, inclusion/exclusion criteria, confidentiality, privacy protections.
  • Assists in communication of study requirements to all individuals involved in the study.
  • Collects documents needed to initiate study and submit to sponsor (ie FDA Forms, CVs, etc)
  • Assists in the informed consent process including interactions with the IRB and discussions with research participants, including answering any questions related to the study. Assures that amended consent forms are appropriately implemented and signed.
  • Screens subjects for eligibility using protocol specific inclusion and exclusion criteria, documenting each potential participant’s eligibility or exclusion.
  • Registers participants to the appropriate coordinating center
  • Registers each participant in the billing matrix to ensure billing of study procedures to the appropriate funding source. Coordinates participant tests and procedures.
  • Collects data as required by the protocol and completes Case Report Forms.
  • Maintains adequate inventory of study supplies. If handling investigational drugs/devices, follows the sponsor protocol and USC Investigational Drug/Device Accountability.
  • Retains all study records in accordance with sponsor requirements and University policies.
  • Maintains effective and ongoing communication with sponsor, research participants and PI during the course of the study.
  • Works with the PI to manage the day to day activities of the study including problem solving, communication and protocol management.

Reporting

  • Promotes the ethical conduct of research by reporting good faith suspicions of misconduct in research as defined within Code of Conduct.
  • Assists PI with scientific and compliance reporting requirements in accordance with Federal regulations and University and sponsoring agency policies and procedures. Assists in the registration (if required) of the study at ClinicalTrials.gov and maintains current information on the site.

Project Closeout

  • Assists PI in submission of accurate and timely closeout documents to applicable Federal agencies, University entities, and the sponsoring agency in accordance with Federal regulations and University and sponsoring agency policies and procedures.
  • Arranges secure storage of study documents that will be maintained according to University policy or for the contracted length of time, whichever is longer.

Financial Management

  • Coordinates appropriate and timely payments to participants (if applicable) in accordance with University policies and procedures.

This is a Non-Exempt position - On-Site

Hourly range

The hourly rate range for this position is $32.01 - $35.00. 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.
Preferred Education: Bachelor's degree
Preferred Experience: 2 Years
Preferred Field of Expertise: Coordinator Training, Knowledge of medical environment and terminology.

                                                  

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$152892.htmld
HQ

University of Southern California Los Angeles, California, USA Office

Los Angeles, CA, United States

University of Southern California Alhambra, California, USA Office

Alhambra, United States

University of Southern California Beverly Hills, California, USA Office

Beverly Hills, United States

University of Southern California Culver City, California, USA Office

Culver City, United States

University of Southern California East Los Angeles, California, USA Office

East Los Angeles, United States, 0

University of Southern California La Habra, California, USA Office

La Habra, United States

University of Southern California Marina del Rey, California, USA Office

Marina del Rey, United States, 0

Similar Jobs

3 Days Ago
In-Office
25-30 Hourly
Junior
25-30 Hourly
Junior
Healthtech • Biotech
Supports clinical study logistics, participant screening and scheduling, study visits, source documentation, data digitization, biospecimen processing, regulatory files, and participant communications. The role also assists with protocol compliance, safety escalation, data analysis, and dissemination while maintaining confidentiality. Work is conducted under senior staff guidance with increasing independence and includes in-person visits at campus and community locations.
Top Skills: Asa24 Diet LogFitbit AppGoogle DriveExcelRedcap
18 Days Ago
In-Office
22-27 Hourly
Entry level
22-27 Hourly
Entry level
Healthtech
Coordinates and administers multiple clinical research studies under general supervision. Supports principal investigators and research staff, implements study protocols, maintains administrative systems, screens and recruits participants, follows study participants, and collects and reports clinical data in accordance with regulatory and institutional requirements. Interacts compassionately with participants diagnosed with various medical conditions and may travel nationally to research sites, investigator meetings, and conferences.
Top Skills: Web-Based Applications
24 Days Ago
In-Office
Los Angeles, CA, USA
32-35 Hourly
Junior
32-35 Hourly
Junior
Big Data
Supports and coordinates clinical cardiology research studies under the direction of principal investigators. Responsibilities include preparing IRB and regulatory submissions, organizing study records, screening and consenting participants, collecting data, completing case report forms, coordinating study procedures, maintaining supplies and compliance documentation, communicating with sponsors and participants, supporting ClinicalTrials.gov registration, assisting with reporting and closeout, and coordinating participant payments.
Top Skills: Clinicaltrials.GovMS Office

What you need to know about the Los Angeles Tech Scene

Los Angeles is a global leader in entertainment, so it’s no surprise that many of the biggest players in streaming, digital media and game development call the city home. But the city boasts plenty of non-entertainment innovation as well, with tech companies spanning verticals like AI, fintech, e-commerce and biotech. With major universities like Caltech, UCLA, USC and the nearby UC Irvine, the city has a steady supply of top-flight tech and engineering talent — not counting the graduates flocking to Los Angeles from across the world to enjoy its beaches, culture and year-round temperate climate.

Key Facts About Los Angeles Tech

  • Number of Tech Workers: 375,800; 5.5% of overall workforce (2024 CompTIA survey)
  • Major Tech Employers: Snap, Netflix, SpaceX, Disney, Google
  • Key Industries: Artificial intelligence, adtech, media, software, game development
  • Funding Landscape: $11.6 billion in venture capital funding in 2024 (Pitchbook)
  • Notable Investors: Strong Ventures, Fifth Wall, Upfront Ventures, Mucker Capital, Kittyhawk Ventures
  • Research Centers and Universities: California Institute of Technology, UCLA, University of Southern California, UC Irvine, Pepperdine, California Institute for Immunology and Immunotherapy, Center for Quantum Science and Engineering

Sign up now Access later

Create Free Account

Please log in or sign up to report this job.

Create Free Account