Impactful Clinical Research Coordinator (Temp Role)

Kelly

Los Angeles (CA)

On-site

USD 39,000 - 41,000

Full time

14 days+
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Benefits offered by this job

Medical benefits
Retirement plan
Paid holidays
Commuter benefits

Job summary

Kelly Science & Clinical is seeking a Clinical Research Coordinator for a 5-month temporary position at a clinical research company in West Hills, CA.

You will coordinate and execute studies, screen and enroll participants, manage data, and ensure regulatory compliance while supporting investigators. Schedule is Monday–Friday, 8am–5pm; pay rate is $28-30/hour. Qualifications include a high school diploma (associate degree preferred) and knowledge of GCP, HIPAA, and FDA regulations.

Qualifications

  • High School Diploma; Associate’s Degree or higher in a health-related field preferred.
  • Basic knowledge of clinical research: GCP, HIPAA, ALCOA principles, FDA regulations, and IATA guidelines. Experience with participant screening and the informed consent process strongly preferred.
  • Medical terminology & patient care experience.

Responsibilities

  • Coordinate and execute clinical research protocols under the guidance of investigators by scheduling and facilitating study visits, procedures, and participant follow-ups.
  • Screen and enroll study participants, assist with the informed consent process, and ensure all interactions follow ethical guidelines and protocol requirements.
  • Collect, record, and maintain accurate clinical data and source documentation in compliance with regulatory and institutional standards.
  • Communicate with study participants to provide education, answer questions, and support adherence to study requirements, while monitoring and reporting adverse events or protocol deviations.
  • Organize and maintain study records, handle laboratory specimens if qualified, and apply critical thinking to resolve issues and support efficient daily operations.
  • Other duties as assigned.

Skills

GCP
HIPAA
ALCOA principles
FDA regulations
IATA guidelines
Participant screening
Informed consent
Medical terminology
Patient care

Education

High School Diploma
Associate’s Degree or higher in a health-related field

Job description

Kelly Science & Clinical is seeking a Clinical Research Coordinator for a 5-month temporary position at a clinical research company in West Hills, CA.

You will coordinate and execute studies, screen and enroll participants, manage data, and ensure regulatory compliance while supporting investigators. Schedule is Monday–Friday, 8am–5pm; pay rate is $28-30/hour. Qualifications include a high school diploma (associate degree preferred) and knowledge of GCP, HIPAA, and FDA regulations.

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