Koreatown/LA, CA- Clinical Research Coordinator

Actalent

Los Angeles (CA)

Hybrid

USD 34,000 - 48,000

Part time

17 hours ago
Be an early applicant

A complete application in a minute

Tailored resume and cover letter, ready to send.

Get past ATS filters

Benefits offered by this job

Medical, dental & vision
401(k) Retirement Plan
Pre-tax and Roth post-tax options
Life Insurance (Voluntary)
Short and long-term disability
Health Spending Account (HSA)
Transportation benefits
Employee Assistance Program
PTO / Vacation or Sick Leave

Job summary

Actalent is seeking a Hybrid Clinical Research Coordinator to support a nasal polyps trial in Koreatown, Los Angeles. The role involves recruiting eligible participants, educating them about the study, and ensuring ongoing engagement and compliance, with a flexible part-time schedule of about 20 hours per week.

Responsibilities include outreach to community and clinics for referrals, pre-screening, and maintaining study documentation, while adhering to HIPAA and GCP standards in a fast-paced

Qualifications

  • Must have proven experience as a Clinical Research Coordinator.
  • Minimum 2 years of patient recruitment experience for clinical trials.
  • Hands-on experience with clinical research processes and trial conduct.
  • Strong recruitment skills including outreach to community and clinical partners.
  • Training in HIPAA regulations and patient privacy requirements.
  • Training in Good Clinical Practice (GCP) guidelines.
  • Excellent verbal and written communication with participants and healthcare professionals.
  • Solid organizational skills with attention to detail for multiple recruitment activities.

Responsibilities

  • Recruit participants through targeted community outreach to raise awareness of the nasal polyps trial.
  • Partner with local clinics and healthcare providers to generate referrals.
  • Educate providers and clinic staff about trial objectives and eligibility.
  • Attend community locations/events to promote the study and identify participants.
  • Pre-screen patients to assess enrollment eligibility.
  • Explain study procedures and expectations to participants clearly.
  • Collaborate with the research team to support study operations and engagement.
  • Maintain accurate documentation per regulatory/site requirements.
  • Apply HIPAA and GCP compliance in all coordination activities.

Skills

Clinical Research Coordinator
Patient recruitment
Clinical trial processes
Recruitment outreach & partnerships
HIPAA training
GCP training
Verbal & written communication
Organizational skills

Job description

Job Title: Hybrid Clinical Research Coordinator
Job Description

This Clinical Research Coordinator role supports a nasal polyps clinical trial at a dedicated research site in Koreatown, Los Angeles. You will focus on identifying and recruiting eligible participants, educating them about the study, and helping ensure their continued engagement and compliance throughout the trial. The position calls for strong clinical research experience, excellent organizational skills, and the ability to communicate confidently and professionally with both participants and research staff. This is a very flexible part-time opportunity, around 20 hours per week.

Responsibilities
  • Perform patient recruitment activities through targeted community outreach efforts to raise awareness of the nasal polyps clinical trial.
  • Partner with local clinics, healthcare providers, and medical professionals to generate patient referrals for the study.
  • Educate providers and clinic staff about the clinical trial objectives, eligibility criteria, and participant qualifications.
  • Visit local community locations and attend community events to promote the study and identify potential participants.
  • Conduct pre-screening of patients to assess eligibility for enrollment in the clinical trial.
  • Communicate clearly with potential participants to explain study procedures, expectations, and the importance of adherence.
  • Collaborate closely with the research team to support smooth study operations and maintain high standards of participant engagement.
  • Maintain accurate documentation related to recruitment, pre-screening, and participant interactions in accordance with regulatory and site requirements.
  • Apply clinical research best practices and compliance standards, including HIPAA and GCP, in all aspects of study coordination.
Essential Skills
  • Proven experience working as a Clinical Research Coordinator.
  • At least 2 years of experience in patient recruitment for clinical trials.
  • Hands-on experience with clinical research and clinical trial processes.
  • Strong skills in patient recruitment, including outreach and relationship-building with community and clinical partners.
  • Training in HIPAA regulations and patient privacy requirements.
  • Training in Good Clinical Practice (GCP) guidelines.
  • Excellent verbal and written communication skills for interacting with participants and healthcare professionals.
  • Solid organizational skills with strong attention to detail in managing multiple recruitment activities.
Additional Skills & Qualifications
  • Experience conducting pre-screening of patients for clinical studies.
  • Experience in community outreach or public-facing roles within healthcare or research settings.
  • Ability to educate and engage medical providers and community members about clinical research studies.
  • Comfort working in a fast-paced research environment with shifting priorities.
  • Strong interpersonal skills and the ability to build trust with diverse participant populations.
Job Type & Location

This is a Contract position based out of Los Angeles, CA.

Pay And Benefits

The pay range for this position is $25.00 - $35.00/hr.

Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.

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)
Job Type & Location

This is a Contract position based out of Los Angeles, CA.

Application Deadline

This position is anticipated to close on Oct 26, 2026.

Workplace Type

This is a hybrid position in Los Angeles,CA.

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 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

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 process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

San Francisco Fair Chance Ordinance

Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

Massachusetts Lie Detector

It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Use of Artificial Intelligence (AI)

We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

Get your free, confidential resume review.

or drag and drop your file here.

Similar jobs

Similar jobs worth comparing

Part-Time Clinical Research Coordinator
Part-Time Clinical Research Coordinator

Actalent • Los Angeles (CA)

On-site
USD 34,000 - 45,000
Competitive hourly pay
On-site work in Los Angeles
Healthcare benefits (eligibility)
Oklahoma City, OK- Clinical Research Coordinator
Oklahoma City, OK- Clinical Research Coordinator

Actalent • United States

Hybrid
USD 34,000 - 48,000
Medical dental vision
401(k) plan
Life Insurance
+2
Clinical Research Coordinator
Clinical Research Coordinator

Actalent • Overland Park (KS)

On-site
USD 34,000 - 48,000
Medical, dental & vision
401(k) Retirement Plan
PTO (Paid Time Off)
+1
Clinical Research Coordinator
Clinical Research Coordinator

Actalent • Rochester (MN)

On-site
USD 52,000 - 62,000
Oklahoma City, OK- Clinical Research Coordinator
Oklahoma City, OK- Clinical Research Coordinator

Actalent • Oklahoma City (OK)

Hybrid
USD 34,000 - 48,000
Medical coverage
Dental/Vision
401(k) plan
+6
Clinical Research Coordinator
Clinical Research Coordinator

Actalent • San Francisco (CA)

On-site
USD 45,000 - 47,000
Medical, dental & vision
401(k) Retirement Plan
Time Off/Leave
Clinical Research Coordinator-hematology
Clinical Research Coordinator-hematology

Actalent • United States

Hybrid
USD 37,195,000 - 48,216,000
Medical, dental & vision
401(k) retirement plan
Life Insurance
Clinical Site Manager
Clinical Site Manager

Actalent • Pasadena (MD)

On-site
USD 62,000 - 96,000
Medical, dental & vision
401(k) Retirement Plan
Paid time off (PTO)
Clinical Research Coordinator
Clinical Research Coordinator

Actalent • Raleigh (NC)

On-site
USD 45,000 - 48,000
Medical, dental & vision
401(k) Retirement Plan
Life Insurance
+5
Clinical Research Coordinator
Clinical Research Coordinator

Talentify • Edison (NJ)

On-site
USD 44,000 - 48,000
Medical, dental & vision
401(k) Retirement Plan
Life Insurance
+1