Multi-Study Clinical Research Coordinator

QuickCruit, Inc.; Dallas (TX); Hybrid; USD 65,000 - 90,000; Full time

Job summary

Empathx in Dallas, TX seeks a Clinical Research Coordinator to lead day-to-day trial activities across multiple protocols. You will coordinate visits, collect data, and ensure adherence to protocol requirements and regulatory standards.

Primary responsibilities include participant recruitment, informed consent, data entry into EDC, and collaboration with investigators and sponsors to support high-quality, compliant trials.

Qualifications

• Experience coordinating multiple protocols across trials in Phases I–IV.
• Familiar with Good Clinical Practice and regulatory requirements.
• Ability to collect data, manage source documents, and maintain regulatory binders.

Responsibilities

• Coordinate and conduct study visits per protocol, obtain informed consent, collect data.
• Perform delegated clinical procedures (e.g., phlebotomy, vital signs) and document results.
• Manage scheduling for three or more concurrent studies across protocols; ensure timelines.

Skills

Study coordination

Clinical data collection

Regulatory documentation

Participant recruitment

GCP experience

Tools

EDC systems

CRF handling

Job description

Empathx in Dallas, TX seeks a Clinical Research Coordinator to lead day-to-day trial activities across multiple protocols. You will coordinate visits, collect data, and ensure adherence to protocol requirements and regulatory standards.

Primary responsibilities include participant recruitment, informed consent, data entry into EDC, and collaboration with investigators and sponsors to support high-quality, compliant trials.