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  1. Home
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  5. Clinical Research Coordinator
Actalent logo

Clinical Research Coordinator

Not Disclosed•ContractorOn-site

location_on10463, Slater Avenue, Colonia Juarez, Fountain Valley, Orange County, California, 92708, United States

Apply Now

About the Team

Actalent is a global leader in engineering and sciences services, connecting visionary companies with specialized experts to drive scale, innovation, and speed to market. With a network of nearly 30,000 consultants and over 4,500 clients across the U.S., Canada, Asia, and Europe, we serve many Fortune 500 organizations. This role is based within a private practice and clinical research site established for over 30 years, known for handling a high volume of sponsor-initiated research studies.

About the Role

As a Clinical Research Coordinator specializing in Dermatology Industry-Initiated Clinical Trials, you will lead and manage the execution of clinical studies under the direction of the Principal Investigator and Site Manager. This position serves as a vital bridge between investigative teams, pharmaceutical sponsors, and research participants, requiring a strong medical background and a deep proficiency in Good Clinical Practices (GCP), FDA regulations, and ethical research standards.

In this fully on-site role, you will work alongside a dedicated team of 7-10 Clinical Research Coordinators and 3-4 Research Assistants, reporting to the Director of Operations. Your day will involve conducting patient visits, collecting and processing biological specimens, performing procedures such as ECGs and vital signs monitoring, and administering study-specific questionnaires. You will ensure strict adherence to study protocols while maintaining accurate case report forms and managing investigational medications with full accountability.

The work environment is designed for collaboration and efficiency, operating from 8 AM to 5 PM with a catered lunch break. The site offers convenient access with a full parking lot, fostering a supportive atmosphere where you can utilize your strong bedside manner to make patients feel comfortable and confident throughout their research journey.

Hiring Process

Applications for this contract position are reviewed on a rolling basis until the anticipated closing date of June 5, 2026. Actalent utilizes Artificial Intelligence (AI) to support parts of the hiring process, including sourcing, screening, and evaluating candidates. While AI tools assist in assessing applications and qualifications, all final hiring decisions are made by the human hiring team. By applying, you acknowledge that your application may be reviewed using these tools.

Equal Opportunity & Culture

Actalent is an equal opportunity employer and considers all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information, or any other characteristic protected by law. We are committed to fostering an inclusive environment where diverse backgrounds are valued.

We adhere to specific legal standards, including the San Francisco Fair Chance Ordinance for relevant positions and Massachusetts laws prohibiting lie detector tests as a condition of employment. If you require a reasonable accommodation due to a disability during the application or interviewing process, please contact actalentaccommodation@actalentservices.com.

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Skills, education and keywords

Skills: Good Clinical Practices, GCP, Fda Regulations, Ecgs, Hipaa, Osha, Sops, Iwrs, Edc Systems, Phlebotomy.

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 for study participants; Schedule and coordinate research visits, assessments, and procedures to ensure protocol adherence; and Manage investigational medications including receiving, dispensing, and performing drug accountability.
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; Bachelor's or Master's degree in a related field; Seasoned experience in clinical research, specifically interventional clinical trials; Proficiency in Good Clinical Practices (GCP); Proficiency in FDA regulations; and Experience with IWRS and EDC systems.
Where is the Clinical Research Coordinator role at Actalent located?expand_more
Clinical Research Coordinator at Actalent is based in 10463, Slater Avenue, Colonia Juarez, Fountain Valley, Orange County, California, 92708, United States. This is a on-site role.
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Work location

Work model: On-site

location_on

10463, Slater Avenue, Colonia Juarez, Fountain Valley, Orange County, California, 92708, United States

Fountain Valley, 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 for study participants
  • check_circleSchedule and coordinate research visits, assessments, and procedures to ensure protocol adherence
  • check_circleManage investigational medications including receiving, dispensing, and performing drug accountability
  • check_circleCollaborate with laboratories to process, ship, and ensure review of investigational reports
  • check_circleActively participate in recruiting and screening study participants for clinical trials
  • check_circleEnsure necessary supplies and equipment are available and functional for each study
  • check_circleConduct patient visits and collect biological specimens such as blood and urine samples
  • check_circleCollect, enter, and manage clinical data while ensuring strict confidentiality
  • check_circleMaintain accurate case report forms and cross-reference patient medical records for FDA compliance

Requirements

  • verifiedHigh School Diploma or GED
  • verifiedBachelor's or Master's degree in a related field
  • verifiedSeasoned experience in clinical research, specifically interventional clinical trials
  • verifiedProficiency in Good Clinical Practices (GCP)
  • verifiedProficiency in FDA regulations
  • verifiedExperience with IWRS and EDC systems
  • verifiedExperience with informed consent processes
  • verifiedExperience in dispensing and reconciling drugs
  • verifiedAbility to create source documents
  • verifiedPhlebotomy certification (preferred)
  • verifiedMA/phlebotomy skills (preferred)
  • verifiedBilingual in Spanish or Vietnamese (preferred)
  • verifiedCCRC certification (preferred)

Nice to Have

MA/phlebotomy skills, bilingual in either Spanish or Vietnamese, Phlebotomy certification, 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_circleLife Insurance including Voluntary Life and AD&D for employee and dependentscheck_circleShort and long-term disability coveragecheck_circleHealth Spending Account (HSA)check_circleTransportation benefitscheck_circleEmployee Assistance Programcheck_circleTime Off/Leave including PTO, Vacation, or Sick Leave
Actalent logo
Company

Actalent

Industry

scientific & qa

View company profilearrow_forwardlanguageWebsite
Quick Overview

Experience

Mid Level

Education

High School Diploma or GED required

Job Type

Contractor

Skills Required

Good Clinical PracticesGCPFda RegulationsEcgsHipaaOshaSopsIwrsEdc SystemsPhlebotomy
arrow_forward
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; Sops; and Iwrs.
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.
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