Study Coordinator I/II

University of Florida•Gainesville, FL

1d•$48,000 - $67,500•Onsite

About The Position

The UF Health Cancer Institute is the 72nd NCI designated cancer center and the only one at a public university in the State of Florida. As a matrix cancer center, we span all of the University of Florida's 16 colleges, pulling together a world-class, multi-disciplinary membership of over 350 faculty and 150 staff to address the challenges of the cancer burden faced by the population we serve as we work together to find a cure. As a Study Coordinator at the UF Health Cancer Institute (UFHCI), you will be responsible for collaborating with coordinators and research staff, investigators, physicians, nurses, and other key personnel in the clinics, hospitals, and the Cancer Institute to ensure compliance with protocol requirements and satisfactory care for patients enrolled on research protocols. In your new role you will be responsible for the following: Coordinating relevant care and protocol required testing for subjects enrolled on an assigned portfolio of human clinical trials. Interpreting and collecting medical and clinical data for prospective and existing enrolled subjects on assigned clinical trials. Maintaining compliance with all internal and external regulatory and institutional requirements related to your trials. Coordinating sample collection, analysis, and shipping for assigned trials. These roles are ideal for candidates with interest in beginning a career in clinical research and/or clinical experience in oncology or other similarly complex disease group and/or clinical research coordination. Employees in these roles operate as part of our collaborative research enterprise and are fundamental to the progress of cancer research being conducted at the University of Florida. A complete job description will be provided to candidates selected for interview.

Requirements

Two or more years of relevant experience and/or training in research and/or oncology.
Experience working with databases and/or subject data.
Proficiency with Microsoft Office applications.
Bachelor’s degree in Health Care, Basic Sciences, or a related field.
Four to six years of relevant experience and/or training in research and/or oncology.
Experience working with databases and subject-level data.
Proficiency with Microsoft Office applications.
Professional clinical research and/or oncology certification (through SOCRA, ACRP, etc.) are required at the earliest of 12 months from hire or eligibility hired in the Clinical Research Coordinator II classification.

Nice To Haves

Bachelor’s degree in Health Care, Basic Sciences, or a related field.
Forward-thinking mentality with the ability to achieve high performance goals and meet deadlines in a fast-paced environment.
Strong desire to establish and maintain effective working relationships with stakeholders and critical staff, both internally and externally, through a variety of communication mediums and venues.
Highly resourceful team-player, with the ability to also be effective independently, maintain appropriate discretion, and utilize effective writing and organizational skills.
Excellent delegation and time management skills and the ability to successfully manage multiple priorities seamlessly with excellent attention to detail.
Strong interpersonal skills, as well as the ability to work with a broad range of people including investigators, physicians, clinic and hospital staff, sponsors, partners at other institutions, UFHCI staff, and others.
Demonstrate understanding and effective use of Emotional Intelligence strategies and skills.

Responsibilities

Coordinating relevant care and protocol required testing for subjects enrolled on an assigned portfolio of human clinical trials.
Interpreting and collecting medical and clinical data for prospective and existing enrolled subjects on assigned clinical trials.
Maintaining compliance with all internal and external regulatory and institutional requirements related to your trials.
Coordinating sample collection, analysis, and shipping for assigned trials.