Clinical Research Coordinator

Lensa; Los Angeles (CA); On-site; USD 50,000 - 85,000; Full time

Job summary

A leading career site seeks a Clinical Research Coordinator in Los Angeles to oversee clinical studies across several therapeutic areas. Ideal candidates will have at least two years of clinical research experience, a bachelor's degree, and certification. Responsibilities include patient recruitment, regulatory management, and coordinating study activities. This is a fully onsite, entry-level position with comprehensive benefits.

Benefits

Medical, dental & vision

401(k) Retirement Plan

Life Insurance

Short and long-term disability

Transportation benefits

Employee Assistance Program

Paid Time Off (PTO)

Qualifications

• 2 years of Clinical Research experience required.
• Experience with multi-site clinical trials or decentralized trials valued.
• Familiarity with regulatory platforms is a plus.

Responsibilities

• Coordinate daily activities for clinical research studies.
• Perform patient-facing duties including consent and recruitment.
• Manage study documentation and support audits.

Skills

Clinical Research

Phlebotomy

Patient Recruitment

Spanish Fluency

Education

Bachelor’s degree

Certified Clinical Research Coordinator (CCRC)

Tools

Clinical Trial Management Systems (CTMS)

Job description

1 week ago Be among the first 25 applicants

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

Clinical Research Coordinator (CRC) to coordinate day-to-day activities for clinical research studies across various therapeutic areas, including ophthalmology, dermatology, and pulmonology.

• Coordinate daily activities for clinical research studies across multiple therapeutic areas.
• Perform direct patient-facing duties, including informed consent, visit scheduling, and follow-up.
• Manage all aspects of patient recruitment and enrollment, including database reviews, outreach, pre-screening, and communications.
• Confidently perform blood draws and handle biospecimen processing and shipping according to protocol requirements.
• Maintain and manage study documentation, source data, and regulatory binders across various systems, including client's CTMS and sponsor EDC systems.
• Support monitoring visits and participate in both internal and external audits.
• Communicate effectively with sponsors, CROs, investigators, and internal departments.
• Provide general support to the team and step in across functions as needed to meet study goals.
  
  

Qualifications

2 years of Clinical Research experience

Bachelor’s degree

Phlebotomy

Certified Clinical Research Coordinator (CCRC) certification

Prior experience with multi-site clinical trials or decentralized trial models

Familiarity with clinical trial management systems (CTMS) and electronic regulatory platforms

Background in therapeutic areas such as Ophthalmology, Dermatology, or Pulmonology

Fluent in Spanish (spoken and written)

Pay and Benefits

The pay range for this position is $50000.00 - $85000.00/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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