Clinical Research Coordinator Associate Trials & Compliance

UT Health San Antonio; San Antonio (TX); On-site; USD 55,000 - 75,000; Full time

Benefits offered by this job

Paid Time Off

Holidays

Discounts

Retirement plan

Job summary

UT Health San Antonio is seeking a Clinical Research Coordinator (CRC) Associate to champion patient safety, protocol integrity, and high-quality clinical trial conduct. Under supervision, you will screen and schedule patients, coordinate all on-study activities, and ensure compliance with study requirements.

The role involves collaborating with investigators, pharmacy, and staff to ensure proper use of investigational products, education of the team, and participation in sponsor meetings to

Qualifications

• Education: Bachelor's degree is required.
• One year of clinical research experience is required.

Responsibilities

• Assists in identifying study objectives and outcomes while adhering to regulations and SOPs.
• Maintains timely communication with the interdisciplinary team to support protocol compliance.
• Collaborates with the PI, pharmacy, and other personnel to ensure proper use of investigational products.
• Provides protocol-specific education to staff.
• Coordinates meetings or teleconferences with sponsors, monitors, and auditors.

Skills

Communication

Organization

Project management

Regulatory knowledge

EDC/CTMS

Education

Bachelor's degree

Job description

UT Health San Antonio is seeking a Clinical Research Coordinator (CRC) Associate to champion patient safety, protocol integrity, and high-quality clinical trial conduct. Under supervision, you will screen and schedule patients, coordinate all on-study activities, and ensure compliance with study requirements.

The role involves collaborating with investigators, pharmacy, and staff to ensure proper use of investigational products, education of the team, and participation in sponsor meetings to