Pamoja Clinical Institute (PCI) is seeking a dependable and detail‑oriented Assistant Clinical Research Coordinator to support our mental health clinical trials in Anaheim. This is a part‑time position with the opportunity to grow into a full‑time role. We’re looking for someone who understands clinical research workflows and can make an immediate contribution.

Responsibilities include:

Scheduling participants and preparing for study visits

Supporting day‑to‑day study visit activities

Maintaining complete and accurate source and regulatory documentation

Entering data and assisting with EDC query resolution

Tracking visit windows, adverse events, and protocol deviations

Preparing study supplies, materials, and equipment

Communicating with sponsors, CRAs, and monitors

Assisting with monitoring visits, audits, and site readiness

Ideal candidates have:
**Previous experience at a clinical research site
**Working knowledge of ICH‑GCP, HIPAA, and FDA regulations
***Familiarity with EDC, CTMS, and electronic regulatory systems
***Excellent attention to detail and time‑management skills
****Ability to support multiple studies and meet deadlines
*****Reliable, professional, and independent work style

Preferred but not required:
Experience in mental health/CNS trials, ACRP/CCRC/SOCRA certification, phlebotomy/ECG/vitals experience, bilingual (English/Spanish).

To apply:
Email your resume and a short introduction to

Subject line: Assistant CRC Application

Employment type:
Part‑time (with potential for full‑time)

Pamoja Clinical Institute (PCI)

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Assistant Clinical Research Coordinator