Clinical Research Coordinator 1

University of Miami•Miami, FL

10d

About The Position

The Clinical Research Coordinator 1 is an entry-level clinical research professional with a basic foundation in clinical research. The role supports data management and implementation of clinical research protocols, demonstrates growing skills and flexibility, and takes responsibility for simple protocols and their timelines. This is a full-time position with the University of Miami/UHealth Hussman Institute in Miami.

Requirements

Bachelor’s degree in a relevant field.
At least 1 year of relevant experience.
Accuracy and attention to detail when completing assignments.
Ability to analyze, organize, and prioritize work under pressure and meet deadlines.
Ability to handle confidential information discreetly.
Ability to work evenings, nights, and weekends as necessary.
Commitment to the University’s core values.
Ability to work independently and/or collaboratively.

Responsibilities

Review charts and pre-screen potential study participants for eligibility; coordinate simple clinical research protocols and maintain enrollment procedures in accordance with the protocol.
Coordinate routine clinical study activities, including collecting and maintaining data, planning timelines, scheduling appointments and study visits, arranging meetings, and evaluating projects.
Perform moderate to complex research tests and experiments under supervision, adapting procedures to support quality improvement.
Follow technical instructions for clinical research equipment and troubleshoot operational failures.
Assist in observing and reporting adverse events to the principal investigator or supervisor, including events reported by study participants.
Address adverse events according to protocol while advocating for participants and maintaining study quality standards.
Identify and report protocol deviations and unanticipated occurrences, and help resolve them.
Follow applicable international, national, and local regulatory requirements.
Understand the contents of and maintain study-specific clinical research regulatory binders.
Maintain required skills and mandatory training in safety, equality, responsible research conduct, continuing education, and research competencies.
Follow University and unit policies and procedures and safeguard University assets.
Perform other duties or responsibilities as necessary.