University of South Florida
Sr. Research Support Specialist (Finance)
This position requires a high school diploma or equivalent and six years of experience in office or administrative support or in research support. College education may be substituted for the required experience on a year for year basis.
Preferred Qualifications:
2-4 years of clinical research experience.
This position is Grant funded and will be a time limited position.The University of South Florida is a high-impact global research university dedicated to student success. Over the past 10 years, no other public university in the country has risen faster in U.S. News and World Report's national university rankings than USF. Serving more than 50,000 students on campuses in Tampa, St. Petersburg and Sarasota-Manatee, USF is designated as a Preeminent State Research University by the Florida Board of Governors, placing it in the most elite category among the state's 12 public universities. USF is a member of the American Athletic Conference.
\n
Working at USF
\n
With more than 16,000 employees at USF, the University of South Florida is one of the largest employers in the Tampa Bay region. At USF you will find opportunities to excel in a rich academic environment that fosters the development and advancement of our employees. We believe in creating a talented, engaged and driven workforce through on-going development and career opportunities. We also offer a first class benefit package that includes medical, dental and life insurance plans, retirement plan options, tuition program and generous leave programs and more.
\n
To learn more about working at USF please visit: Work Here. Learn Here. Grow Here .The Senior Research Support Specialist will perform a wide variety of administrative support duties.
This position will participate in specialty clinic, coordinating with clinic staff and physicians to evaluate
patients that might be consider for research studies. Collect, analyzes and performs quality assurance
of study data. Monitors overall clinical study to in sure that quality control measures are in compliance
with protocol. Actively participates in research study meetings to discuss progress/status of study.
Ensures consistent interpretation and adherence to protocols at all stages of trials by team.
\n
Evaluates potential research participants with Principal Investigator; schedules screening evaluations;
explains consent process; performs required screening evaluations; randomizes participants into
appropriate research study. Coordinates and schedules study visit and follow-ups. Oversees or
performs required procedures for each visit. Records data on each study participant for each visit
according to research protocol, maintaining complete study progress notes and case report from for
each visit. Reports any Adverse Event according to protocol.
\n
Data entry for clinical trials, proofing for data entry errors, and preparing patient/participant documents
for study visits,which includes development of source documents as needed. Assist with monitoring visits
and attend Investigator Meetings as requested by the Assistant Director. Develop materials to
communicate projects/trials to potential clients and their families and assist with the promotional
materials supplied by the sponsors. Conducts patient visits and testing,including preparation of laboratory
shipments and obtaining required information from study subjects during patients visits.
\n
Oversees site inventory of supplies for the division (lab kits, pre medication,
patient specific supplies, office supplies).
\n
Assist in training of new or more junior clinical research staff members. Aids
clinical staff in addressing continued patient care (calls to discuss AEs, medication
questions, etc) and may be called upon to assist during clinic hours with various
providers.