Clinical Research Coordinator – Translational Trials

Vanderbilt University Medical Center; Nashville (TN); On-site; USD 60,000 - 75,000; Full time

Job summary

Vanderbilt University Medical Center in Nashville, TN seeks a Clinical/Translational Research Coordinator II to coordinate approval processes and conduct of clinical/translational research, ensuring integrity and compliance with policies and federal regulations.

The role involves preparing IRB submissions, maintaining documentation for sponsors and authorities, supporting recruitment, and coordinating across study sites with focus on participant safety and data quality.

Qualifications

• Proficiently prepares and processes new IRB research proposals, amendments, continuing review applications and adverse event reports according to institutional and departmental policies and procedures and federal regulations.
• Maintains documents required to be available for regulatory authorities and sponsors before, during and after trials.
• Assists in site visits to review research, source documentation and procedures.

Responsibilities

• Proficiently prepares and processes new IRB proposals and amendments.
• Maintains regulatory documents for authorities and sponsors.
• Assists in site visits to review research procedures and source data.
• Identifies equipment and supplies needed to fulfill project requirements across sites.
• Participates in determining participant eligibility and recruitment strategies.

Skills

Clinical Research

Study Design

Project Coordination

Job description

Vanderbilt University Medical Center in Nashville, TN seeks a Clinical/Translational Research Coordinator II to coordinate approval processes and conduct of clinical/translational research, ensuring integrity and compliance with policies and federal regulations.

The role involves preparing IRB submissions, maintaining documentation for sponsors and authorities, supporting recruitment, and coordinating across study sites with focus on participant safety and data quality.