Senior Clinical Research Coordinator

Responsibilities

• Cover day-to-day operations of clinical trials following GCP, study protocols, and regulations.
• Organize processes and study team activities to meet research objectives.
• Manage study visits, research procedures, and follow-up.
• Develop and maintain tracking tools and documentation; report study metrics to management.
• Support all stages of study visits: pre-study, qualification, initiation, monitoring, and close-out.
• Maintain source documentation and report adverse events.
• Recruit, screen, consent, and enroll participants.
• Collect and maintain patient and lab data.
• Act as liaison among participants, families, departments, external organizations, and government agencies.

Requirements

• Minimum of a bachelor's degree or equivalent in a relevant field.
• At least 8 years of directly related work experience, or a master's degree or equivalent with 6 years of directly related work experience.

Qualifications

• Experience coordinating day-to-day operations of clinical trials.
• Ability to manage study visits and research procedures.
• Knowledge of regulatory guidelines and Good Clinical Practice (GCP).
• Strong organizational and communication skills.

Skills

• Excellent organizational and time management skills.
• Strong interpersonal and communication skills.
• Proficiency in data management and reporting.
• Ability to work independently and as part of a team.

Benefits

The University of Utah offers a comprehensive benefits package including health insurance, retirement plans, and paid time off.

Pay

$68K-$72K

Schedule

Full Time