Clinical Research Coordinator 1

University of Miami•Miami, FL

9d•Onsite

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 or implementation of clinical research protocols, applies developing skills and flexibility, and takes responsibility for simple protocols and timelines. The position is full-time and based in Miami at the University of Miami/UHealth Hussman Institute. The duties listed may be expanded to include other responsibilities as needed.

Requirements

Bachelor’s degree in a relevant field.
Minimum of 1 year of relevant experience.
Skill in completing assignments accurately and with attention to detail.
Ability to analyze, organize, and prioritize work under pressure while meeting deadlines.
Ability to process and handle confidential information with discretion.
Ability to work evenings, nights, and weekends as necessary.
Commitment to the University’s core values.
Ability to work independently and/or in a collaborative environment.

Responsibilities

Perform chart reviews and prescreening to assess study participant eligibility and coordinate simple clinical research protocols.
Maintain participant enrollment procedures in accordance with study protocols.
Coordinate routine clinical study activities, including data collection and maintenance, planning timelines, scheduling appointments and study visits, arranging meetings, and evaluating projects.
Perform moderate to complex research tests or experiments and adapt procedures for quality improvement under supervision.
Follow technical instructions for operating clinical research equipment and troubleshoot operational failures.
Assist in observing and informing the principal investigator or supervisor about adverse events, including those reported by study participants.
Address adverse events according to protocol and advocate for study participants and quality standards throughout the study.
Identify, report, and help resolve protocol deviations and unanticipated occurrences.
Follow applicable international, national, and local regulatory requirements.
Understand the contents and maintenance requirements of study-specific clinical research regulatory binders.
Maintain required skills and mandatory training in safety, equality, responsible conduct of research, continuing education, and research competencies.
Follow University and unit-level policies and procedures and safeguard University assets.