Clinical Research Coordinator — Impactful Trials & Ops

Medix™; Texas; Presencial; USD 54.000 - 76.000; Jornada completa

Descripción de la vacante

Medix is seeking a detail-oriented Clinical Research Coordinator in Live Oak, TX to drive study operations, maintain protocol compliance, and manage active trial execution across a dynamic clinical caseload.

The role requires 3+ years of CRC experience, patient-facing research work (e.g., MA/EMT/Phlebotomy), and the ability to support multiple studies simultaneously, coordinating informed consent, IP handling, data entry, and regulatory communications, while upholding HIPAA and FDA GCP

Formación

• 3+ years of clinical research experience as a CRC.
• Experience in a patient-facing research role, or as a Medical Assistant, EMT, or Phlebotomist.
• Ability to support and manage at least 3 active studies simultaneously (industry-funded and IIT).

Responsabilidades

• Coordinate all aspects of participant care from screening through study completion, including informed consent and education on IP use and safety.
• Dispense and administer IP and promptly report adverse events, deviations, and safety issues to the PI, Sponsor, and IRB.
• Perform data collection, source documentation, and entry into databases, sponsor CRFs, and IWRS with proper documentation.
• Collaborate with the clinical team and external partners to achieve target enrollment and efficient trial selection.
• Assist in site initiation meetings, monitoring visits, and regulatory inspections.
• Manage patient stipend payments and ensure HIPAA, FDA GCP, and QA guidelines compliance.

Conocimientos

CRC experience

Multitask study management

Patient-facing research

Descripción del empleo

Medix is seeking a detail-oriented Clinical Research Coordinator in Live Oak, TX to drive study operations, maintain protocol compliance, and manage active trial execution across a dynamic clinical caseload.

The role requires 3+ years of CRC experience, patient-facing research work (e.g., MA/EMT/Phlebotomy), and the ability to support multiple studies simultaneously, coordinating informed consent, IP handling, data entry, and regulatory communications, while upholding HIPAA and FDA GCP