Clinical Research Coordinator: Drive Study Excellence

Utmb; Galveston (TX); On-site; USD 52,000 - 78,000; Full time

Job summary

UTMB Health in Galveston seeks a Clinical Research Coordinator to support clinical studies by collecting human subject data per study protocol and performing general administrative duties.

The role emphasizes GCP activities, regulatory compliance, site initiation visits, maintaining source documents, and coordination with investigators to recruit and monitor participants, while ensuring quality and protocol adherence.

Qualifications

• Bachelor's degree or equivalent and two years of directly related experience.
• Knowledge of Good Clinical Practice (GCP) and regulatory activities.
• Experience scheduling and coordinating site visits and study initiation.
• Ability to review patient eligibility and abstract relevant data from sources.

Responsibilities

• Applies knowledge in GCP activities and regulatory tasks.
• Schedules and coordinates pre-site visits and site initiation visits.
• Maintains source documentation and forms per protocol for quality and accuracy.
• Reconciles study drug accountability and maintains temperature/QC logs.
• Identifies and recruits clinical research subjects and monitors enrollment goals.
• Mentors new coordinators and assists with IRB submissions.
• Assists with grant/protocol preparation and IRB stipulations.

Skills

GCP knowledge

Regulatory compliance

Clinical coordination

Education

Bachelor's degree or equivalent

Two years related experience

Job description

UTMB Health in Galveston seeks a Clinical Research Coordinator to support clinical studies by collecting human subject data per study protocol and performing general administrative duties.

The role emphasizes GCP activities, regulatory compliance, site initiation visits, maintaining source documents, and coordination with investigators to recruit and monitor participants, while ensuring quality and protocol adherence.