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  1. Home
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  3. scientific & qa
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  5. Clinical Research Coordinator
Actalent logo

Clinical Research Coordinator

Not Disclosed•ContractorOn-site

location_onWest Centennial Road, Santa Ana Gardens, Santa Ana, Orange County, California, 92704, United States

Apply Now

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.

About the Role

As a Clinical Research Coordinator, you will lead and manage clinical trials in strict compliance with regulatory standards. Working closely with the investigative team, pharmaceutical sponsors, and research participants, you will ensure the integrity of the study from start to finish. This role is designed for professionals with strong medical experience who are committed to ethical research standards and proficient in Good Clinical Practices (GCP) and FDA regulations.

In this fully onsite position based in Fountain Valley, CA, you will serve as a vital link between the Principal Investigator, the site, and the participants. Your day-to-day involves conducting patient visits, collecting and processing biological specimens, and performing procedures such as ECGs and vital signs monitoring. You will coordinate research visits and assessments, ensuring all protocol requirements are met while maintaining accurate case report forms and cross-referencing patient medical records for completeness.

Beyond clinical execution, you will manage investigational medications, collaborate with laboratories for specimen processing, and actively participate in recruiting and screening study participants. Your work ensures that all regulatory documentation is up to date, supplies are functional, and the study adheres to company policies, HIPAA, OSHA regulations, and Standard Operating Procedures (SOPs).

Hiring Process & Application

This is a contract position with an anticipated application deadline of June 5, 2026. We utilize 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.

Equal Opportunity & Culture

Actalent 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.

We are committed to inclusivity and reasonable accommodations. 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.

Note: 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. Additionally, it is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment.

Work location

Work model: On-site

location_on

West Centennial Road, Santa Ana Gardens, Santa Ana, Orange County, California, 92704, United States

Santa Ana, California

Key Responsibilities

  • check_circleManage and oversee the execution of clinical trials under the direction of the Principal Investigator
  • check_circlePerform clinical procedures including ECGs and vital signs monitoring
  • check_circleSchedule and coordinate research visits, assessments, and procedures for participants
  • check_circleCollect, enter, and manage clinical data while ensuring participant confidentiality
  • check_circleManage investigational medications including receiving, dispensing, and drug accountability
  • check_circleCollaborate with laboratories to process, ship, and review investigational reports
  • check_circleParticipate in recruiting and screening study participants
  • check_circleEnsure necessary supplies and equipment are available and functional for each study
  • check_circleComply with HIPAA, OSHA regulations, and Standard Operating Procedures to deliver high-quality services

Requirements

  • verifiedHigh School Diploma or GED
  • verifiedPrevious experience conducting clinical trials
  • verifiedCertification as a Clinical Research Coordinator (CCRC) preferred
  • verifiedProficiency in Good Clinical Practices (GCP)
  • verifiedKnowledge of FDA regulations
  • verifiedKnowledge of HIPAA regulations
  • verifiedKnowledge of OSHA regulations

Nice to Have

Bachelor's or Master's degree in a related field. Certification as a Clinical Research Coordinator (CCRC).

Benefits & Perks

check_circleMedical, dental, and vision insurancecheck_circleCritical Illness, Accident, and Hospital insurancecheck_circle401(k) Retirement Plan with pre-tax and Roth post-tax contributionscheck_circleVoluntary Life and AD&D insurance for employee and dependentsShort and long-term disability insurance
Actalent logo
Company

Actalent

Industry

scientific & qa

View company profilearrow_forward
Quick Overview

Experience

Mid Level

Education

High School Diploma or GED required

Job Type

Contractor

Skills Required

Good Clinical Practices

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Skills, education and keywords

Skills: Good Clinical Practices, GCP, Fda Regulations, Ecgs, Hipaa, Osha, Standard Operating Procedures, Sops, CCRC.

Education: High School Diploma or GED required; Bachelor's degree in a related field preferred; Master's degree in a related field preferred.

Frequently asked questions about Clinical Research Coordinator at Actalent

What does a Clinical Research Coordinator at Actalent do?expand_more
A Clinical Research Coordinator at Actalent is responsible for the following: Manage and oversee the execution of clinical trials under the direction of the Principal Investigator; Perform clinical procedures including ECGs and vital signs monitoring; Schedule and coordinate research visits, assessments, and procedures for participants; and Collect, enter, and manage clinical data while ensuring participant confidentiality.
What are the requirements for this Clinical Research Coordinator role?expand_more
Actalent is looking for candidates who meet the following requirements: High School Diploma or GED; Previous experience conducting clinical trials; Certification as a Clinical Research Coordinator (CCRC) preferred; Proficiency in Good Clinical Practices (GCP); Knowledge of FDA regulations; and Knowledge of HIPAA regulations.
Where is the Clinical Research Coordinator role at Actalent located?expand_more
Clinical Research Coordinator at Actalent is based in West Centennial Road, Santa Ana Gardens, Santa Ana, Orange County, California, 92704, United States. This is a on-site role.
Is this Clinical Research Coordinator job remote, hybrid, or on-site?expand_more
Actalent has listed this Clinical Research Coordinator role as on-site.
How much experience is required for this Clinical Research Coordinator role?expand_more
Candidates for Clinical Research Coordinator at Actalent should have mid level.
What skills do you need for the Clinical Research Coordinator role at Actalent?expand_more
Key skills for Clinical Research Coordinator at Actalent include Good Clinical Practices; GCP; Fda Regulations; Ecgs; Hipaa; Osha; Standard Operating Procedures; and Sops.
What education is required for Clinical Research Coordinator at Actalent?expand_more
Educational requirements for this role: High School Diploma or GED required; Bachelor's degree in a related field preferred; and Master's degree in a related field preferred.
What category does the Clinical Research Coordinator role belong to?expand_more
Clinical Research Coordinator at Actalent is part of the scientific & qa job category on Recrutus.
Recrutus

Curating the world's most innovative career opportunities. We bridge the gap between visionary talent and industry-leading companies.

Search roles by city, category, skill, or job type — explore verified US employers, salary benchmarks, and remote-friendly teams hiring nationwide.

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  • check_circleConduct patient visits and collect biological specimens such as blood and urine samples
  • check_circleMaintain accurate case report forms and cross-reference patient medical records for FDA compliance
  • check_circle
    check_circleHealth Spending Account (HSA)
    check_circleTransportation benefits
    check_circleEmployee Assistance Program
    check_circleTime Off/Leave including PTO, Vacation, or Sick Leave
    GCP
    Fda Regulations
    Ecgs
    Hipaa
    Osha
    Standard Operating Procedures
    Sops
    CCRC
    Accessibility