Clinical Research Coordinator

Lensa; Los Angeles (CA); On-site; USD 60,000 - 80,000; Full time

Job summary

A leading career site is looking for a Clinical Research Coordinator in Los Angeles, CA. In this fully onsite role, you will support clinical trials by performing various administrative tasks, scheduling interviews, and ensuring compliance with research protocols. The ideal candidate will have a strong background in clinical research, with a minimum of one year of experience, and proficiency in EHR systems and Microsoft Office.

Benefits

Medical, dental & vision

401(k) Retirement Plan

Employee Assistance Program

Time Off/Leave

Qualifications

• Minimum 1 year of experience as a Clinical Research Coordinator.
• Experience with EHR/EMR systems and Microsoft Office Suite required.

Responsibilities

• Assists CRCs and PIs with administrative tasks related to clinical trials.
• Conducts participant interviews and manages appointment scheduling.
• Enters participant data into a database and assists with regulatory management.

Skills

Clinical Research Coordination

EHR/EMR Systems

Customer Service

Microsoft Office Suite

Education

High school diploma or GED

Job description

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Lensa is the leading career site for job seekers at every stage of their career. Our client, Actalent, is seeking professionals in Los Angeles, CA. Apply via Lensa today!

Clinical Research Coordinator

Schedule & Travel

Onsite Monday-Friday 8 am-5 pm

Duties

• Assists the CRCs and PIs with all administrative tasks related to clinical research trials
• Conducts telephone or in-person interviews with participants including screening for eligibility
• Performs follow-up for appointments and manages scheduling of appointments (by telephone, e-mail, and/or mail) with study participants
• Prepares, mails and processes questionnaires and other study correspondence
• Assist in tracking study participants using MS Excel
• Keeps accurate and detailed records and files of work
• Reviews, edits, cleans, and enters participant data into a database
• Assists with regulatory management
• May assist with literature reviews for proposal submissions and manuscript preparation
• Bookkeeping related to study budgets (ordering supplies, requesting checks for payment & participant incentives)
• Miscellaneous administrative tasks (typing labels, copying, faxing, meeting preparation, note-taking, transcribing audio files, etc.)
  
  

Qualifications

• MUST have a minimum of 1 year of Clinical Research Coordinator
• MUST have experience with EHR/EMR systems
• MUST have experience with Microsoft Office Suite (Outlook, Excel, Word, etc.)
• Customer service experience
• High school diploma or General Education Development (GED) required
  
  

Pay and Benefits

The pay range for this position is $25.00 - $30.00/hr.

Requirements

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:

• Medical, dental & vision
• Critical Illness, Accident, and Hospital
• 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
• Life Insurance (Voluntary Life & AD&D for the employee and dependents)
• Short and long-term disability
• Health Spending Account (HSA)
• Transportation benefits
• Employee Assistance Program
• Time Off/Leave (PTO, Vacation or Sick Leave)
  
  

Workplace Type

This is a fully onsite position in Los Angeles,CA.

Application Deadline

This position is anticipated to close on Jun 6, 2025.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email [e-mail] ([e-mail]) for other accommodation options.

Seniority level

• Seniority level

  Entry level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Research, Analyst, and Information Technology

• Industries

  IT Services and IT Consulting

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