Senior Clinical Research Coordinator - Lead Study Ops

The University of Texas Medical Branch; Galveston (TX); On-site; USD 65,000 - 95,000; Full time

Job summary

The University of Texas Medical Branch in Galveston is seeking a Senior Clinical Research Coordinator to manage clinical research projects for Principal Investigators by gathering patient data via methods specified in the study protocol. Provides complex administrative duties in support of the study to insure compliance with regulations.

The role involves regulatory submissions (IRB), subject recruitment, data collection, and mentoring research staff while ensuring quality documentation and

Qualifications

• Bachelor’s degree and five years of clinical research coordinator experience or equivalent.
• Experience ensuring compliance with regulatory requirements.
• Strong data collection and regulatory document handling.

Responsibilities

• Applies knowledge in contributing to GCP activities and regulatory activities.
• Under the direction of the PI, assists with the preparation and submission of IRB and regulatory documents.
• Attends Investigator meetings and coordinates study initiation.
• Identifies and recruits clinical research subjects and monitors enrollment goals.
• Develops source documentation and tools for protocol implementation and teaches staff how to use them.
• Maintains accurate source documentation and regulatory forms with quality assurance.

Skills

GCP knowledge

Regulatory submissions

Study coordination

Subject recruitment

Education

Bachelor's degree

Job description

The University of Texas Medical Branch in Galveston is seeking a Senior Clinical Research Coordinator to manage clinical research projects for Principal Investigators by gathering patient data via methods specified in the study protocol. Provides complex administrative duties in support of the study to insure compliance with regulations.

The role involves regulatory submissions (IRB), subject recruitment, data collection, and mentoring research staff while ensuring quality documentation and