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Non-Clinical Research Associate

Job in California, Moniteau County, Missouri, 65018, USA
Listing for: 6AM City, LLC
Full Time position
Listed on 2026-07-23
Job specializations:
  • Research/Development
    Clinical Research
  • Healthcare
    Clinical Research
Salary/Wage Range or Industry Benchmark: 25 - 30 USD Hourly USD 25.00 30.00 HOUR
Job Description & How to Apply Below
Location: California

Job Description

Non-Clinical Research Associate

Onsite in Los Angeles, CA 90024

Monday to Friday, 8:00 AM to 5:00 PM

Contract - Approximately (12 weeks)

Compensation: $25 - $30 per hour (based on experience)

LHH is seeking a highly skilled and experienced Research Associate to join our dynamic team in Los Angeles, CA. As a Non-Clinical Research Associate, you will play a key role in managing and coordinating research projects, ensuring compliance with regulatory standards, and mentoring junior research staff. This is an excellent opportunity for individuals with a strong background in data management, clinical research coordination, and administrative tasks to contribute to meaningful scientific advancements.

Responsibilities
:

  • Oversee and manage research projects, ensuring adherence to timelines and protocols

  • Perform data management tasks, including data collection, entry, cleaning, and analysis

  • Conduct basic clinical research activities, including subject recruitment, informed consent processes, and data monitoring

  • Coordinate and support study logistics, such as scheduling appointments, arranging site visits, and coordinating with study participants and investigators

  • Assist in the preparation and submission of regulatory documents for Institutional Review Board (IRB) approvals

  • Train and mentor junior research staff, providing guidance on research methodologies, data management, and Good Clinical Practice (GCP) guidelines

  • Collaborate with cross-functional teams, including investigators, sponsors, and external partners

  • Maintain accurate and up-to-date study documentation, ensuring compliance with regulatory requirements

  • Participate in study-related meetings, conferences, and presentations as necessary

Qualifications
:

  • Minimum of 5 years of experience in data management, basic clinical research coordination, AND administrative tasks within a research or healthcare setting

  • Strong knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirements

  • Proficiency in data management and statistical analysis software (e.g., Microsoft Excel, SPSS, SAS)

  • Excellent organizational and time management skills with the ability to prioritize tasks effectively

  • Strong attention to detail and ability to maintain accurate and complete records

  • Effective communication and interpersonal skills, with the ability to work collaboratively in a team-oriented environment

  • Demonstrated ability to mentor and train others

  • Bachelor's degree in a relevant field (e.g., life sciences, public health, nursing) is required; advanced degree is preferred

Pay Details: $25.00 to $30.00 per hour

Search managed by: Katherine Geanetta

Benefit offerings available for our associates include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, EAP program, commuter benefits and a 401K plan. Our benefit offerings provide employees the flexibility to choose the type of coverage that meets their individual needs. In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other paid leave required by Federal, State, or local law, as well as Holiday pay where applicable.

Equal Opportunity Employer/Veterans/Disabled

To read our Candidate Privacy Information Statement, which explains how we will use your information, please navigate to

The Company will consider qualified applicants with arrest and conviction records subject to federal contractor requirements and/or security clearance requirements.

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Position Requirements
10+ Years work experience
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