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Full Time Clinical Research Coordinator Exp. w/ Drug Studies

Job

Allergy and Asthma Associates of Southern California

Laguna Niguel, CA (In Person)

Full-Time

Posted 2 days ago (Updated 2 hours ago) • Actively hiring

Expires 6/22/2026

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Job Description

Full Time Clinical Research Coordinator Exp. w/ Drug Studies Allergy & Asthma Associates of Southern California dba. Southern California Research 28202 Cabot Road, Laguna Niguel, CA 92677 Job details
Pay:
$24 - $28 an hour Job type: Full-time Shift and schedule 8-hour shift Monday to Friday Expected hours: 40 per week
Experience:
Clinical Research Coordinator:
1 year (Required)
Work Location:
In person Benefits 401(k) Health insurance Paid time off Vision insurance Dental insurance Full job description Must have clinical drug study experience. We are a fast-paced research center currently looking to add an experienced research coordinator to our staff. Ideal candidates will possess the following qualifications: Experience as a clinical research coordinator Ability to work as a team member Self -starter and ability to work independently Excellent communication skills, written and verbal Organized and attention to detail, ability to work in a fast-paced environment Ability to adapt to changing schedules Supply and inventory management Third party vendor management Facilitate monitoring visits (IMVs) and sponsor correspondence including managing the follow-up process IP management, dispensation, and accountability Adverse Event management, tracking, reporting, and follow-up Able to review study protocols, create source documents, maintain regulatory binders Conduct patient recruitment and enrollment of eligible patients Experience consenting, screening and randomizing subjects Ability to multitask, prioritize and identify urgent matters Able to obtain vital signs, ECG's, give injections Phlebotomy certified, IATA certified and experience processing labs Computer skills—including used of Microsoft Office Suite CCRC or working towards obtaining certification. GCP Certification is required at the very least Understands GCP, ICH and FDA guidelines and requirements This role is 100% onsite. Candidates must be willing to relocate before starting work if not already located in the area.

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