Clinical Research Coordinator - Per Diem

University of Miami•Miami, FL

3d•Onsite

About The Position

The Department of Clinical Translational Research Site has an exciting opportunity for a per-diem Clinical Research Coordinator to work on-site in Miami. The Clinical Research Coordinator provides professional level support for research clinical studies involving human subjects and assists in the design of studies, generation of databases, and update and maintenance of documentation. Moreover, the Clinical Research Coordinator develops, verifies, and implements procedures to accomplish research goals.

Requirements

Bachelor’s degree in relevant field required
Minimum 3 years of relevant experience required
Learning Agility: Ability to learn new procedures, technologies, and protocols, and adapt to changing priorities and work demands.
Teamwork: Ability to work collaboratively with others and contribute to a team environment.
Technical Proficiency: Skilled in using office software, technology, and relevant computer applications.
Communication: Strong and clear written and verbal communication skills for interacting with colleagues and stakeholders.

Responsibilities

Coordinates routine activities of clinical studies, including data maintenance, grant expenditure adherence, project evaluation, meeting scheduling, and research subject interfacing.
Tracks medical reports and reviews regulatory documents to generate reports.
Serves as project liaison to other departments, outside organizations, government agencies, and product representatives.
Recruits patients into the study and reviews on a weekly basis the percentage recruited.
Reviews data collected and inserts into the study dataset.
Compares the data collected to the monitored phone calls for data quality assurance.
Evaluates and monitors timelines for studies and for each subject participant to comply with applicable protocols.
Prepares materials for the brochures and retaining letters and mails to appropriate members according to their time in the study.
Administers informed consent forms for patients on drug studies.
Maintains pool of study candidates and ensures their availability.
Coordinates the necessary testing for patient evaluations per physicians’ orders and study protocol requirements.
Adheres to University and unit-level policies and procedures and safeguards University assets.