Clinical Research Coordinator - Patient-Centric Trials

Medix™

San Antonio (TX)

In loco

USD 60.000 - 80.000

Tempo pieno

5 giorni fa

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Descrizione del lavoro

Medix™ is seeking a detail-oriented Clinical Research Coordinator in San Antonio, TX to drive study operations, ensure protocol compliance, and manage active trial execution across a dynamic caseload. You will coordinate participant care from screening to completion, obtain informed consent, administer IP, and monitor safety, with strong collaboration across the clinical team and external partners.

This role emphasizes data integrity, regulatory compliance, and enrollment success, requiring

Competenze

3+ years of clinical research experience as a CRC supporting investigational drug studies.
Experience in a patient-facing research role or as a Medical Assistant, EMT, or Phlebotomist.
Proven ability to manage at least 3 active studies concurrently.

Mansioni

Coordinate all aspects of participant care from screening through study completion, including informed consent.
Dispense and administer IP, track and report adverse events and deviations.
Data collection, source documentation, and entry into sponsor CRFs and IWRS.
Collaborate with the clinical team and external partners to support recruitment and enrollment goals.
Assist with site initiation, monitoring visits, and regulatory inspections.
Manage patient stipend payments and ensure HIPAA and FDA GCP compliance.