Clinical Research Coordinator I

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

Job summary

Lensa is seeking a Clinical Research Coordinator I for entry-level support of clinical trials in Los Angeles. The ideal candidate will gain valuable hands-on experience and mentorship within a clinical operations team, facilitating patient interaction and contributing to study coordination. Strong interpersonal and organizational skills are essential.

Benefits

Medical, dental & vision

401(k) Retirement Plan

Short and long-term disability

Health Spending Account (HSA)

Employee Assistance Program

Time Off/Leave (PTO, Vacation or Sick Leave)

Qualifications

• Experience as a medical assistant, phlebotomist, EMT, CNA, or LPN.
• Ability to multitask in a detail-oriented environment.
• Comfort with technology and learning EDC systems.

Responsibilities

• Support patient scheduling, check-ins and follow-up communications.
• Assist in executing clinical trial activities under guidance.
• Enter and maintain accurate study data.

Skills

Interpersonal skills

Organizational skills

Basic medical terminology knowledge

Education

Prior medical or clinical experience

Job description

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Description

Overview:

We are seeking a driven and adaptable Clinical Research Coordinator I (CRC I) to support clinical trials across multiple locations. This is an entry-level role designed for candidates with a hands-on medical background and strong patient interaction experience, such as medical assistants, phlebotomists, EMTs, or similar roles. As a CRC I, you will be part of a growing clinical operations team, gaining direct experience in the coordination of clinical trials. This position offers hands-on learning, mentorship, and full support in developing your clinical research skills.

Key Responsibilities Include (but Are Not Limited To)

• Assist in executing clinical trial activities under the guidance of experienced team members
• Support patient-facing responsibilities including scheduling, check-ins, and follow-up communication
• Participate in subject screening, enrollment, and retention efforts
• Enter and maintain accurate study data, and assist with resolving queries in electronic data capture (EDC) systems
• Attend site initiation visits and investigator meetings as needed
• Prepare and organize study documentation, source materials, and regulatory files
• Coordinate appointment scheduling and assist in ensuring visit compliance
• Communicate with site staff, patients, and sponsor or CRO representatives
• Travel between locations and satellite sites as needed
  
  

Required Qualifications

Additional Skills & Qualifications

• Prior medical or clinical experience in a patient-facing role (e.g., MA, phlebotomist, EMT, CNA, LPN, etc.)
• Strong interpersonal and organizational skills
• Basic familiarity with medical terminology or healthcare procedures
• Comfort with technology and ability to learn EDC systems
• Ability to multitask in a dynamic, detail-oriented environment
• Willingness to travel to support multiple study sites
  
  

Preferred Qualifications

• Fluent in Spanish (spoken and written)
• Familiarity with clinical trial management systems (CTMS) and electronic regulatory platforms
• Background in therapeutic areas such as Ophthalmology, Dermatology, or Pulmonology
  
  

Pay and Benefits

The pay range for this position is $24.00 - $26.00/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 13, 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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