Clinical Research Coordinator II - Stroke/Neurovascular Research

University of Florida
Florida, United States
Salary Not Specified
Posted Date
Jun 28, 2022

View more

Position Type
Faculty Positions, Health & Medicine, Medicine, Other Health & Medicine, Administrative, Academic Affairs, Research Administration
Employment Type
Full Time

Classification Title:

Clinical Research Coord II

Job Description:

The University of Florida's Department of Neurology, Division of Neurovascular is looking for clinical research coordinators who want to further the mission of research and pursue the prevention and treatment of stroke and other neurovascular disorders. We are seeking candidates with at least 2 years of human subject research, who are passionate about clinical care, comfortable in a clinical environment, detailed-oriented, motivated, and adept at working collaboratively with to meet shared goals and objectives. The Clinical Research Coordinator II is responsible for the daily operations of clinical trial studies run by the Neurovascular Division. Responsible for ensuring that all required regulatory documentation is completed and submitted as appropriate for all research/clinical trial activity which includes, but is not limited to, new submissions, continuing reviews, and revisions through the University of Florida Health Professions IRB and a central IRB.

Duties to include:

Responsible for all administrative aspects of investigator clinical research and regulatory operations of assigned clinical trials run by the Neurovascular Division as well as assisting with the other research studies as needed. Ensures all required regulatory documentation is completed and submitted as appropriate for all research/clinical trial activity which includes, but is not limited to, new submissions, continuing reviews, and revisions through the University of Florida Health Professions IRB and a central IRB. Interprets and explain all contractual terms, FDA and IRB regulations. Interprets research client care, treatment, administrative rules and policies and for recommending new and improved programs to effectively manage research client care and treatment administration. Responsible for management of data and filing systems for ongoing protocols.

In charge of recruiting patients for various studies and responsible for following protocols as outlined, which may include, but is not limited to, screening, administering questionnaires, developing standardized scales for clinical data collection, and giving standardized cognitive and motor tests. Schedules research patients in EPIC (appointment confirmation and reminders). Assist with specimen processing, storage, and shipment. Enters data into a database/source binder/case report forms (CRFs) and reports all adverse events.

Corresponds with sponsors and assists with monitoring visits and other meetings with regulatory bodies. Work on other research activities as assigned, and ensures that all research activities are administered appropriately.

Participates in patient, community and health care provider education to include presentations and seminars. Attend research study conferences/meetings as a representative of the Department of Neurology.

Clinical trials are a crucial part of our clinical research program, which seeks to determine the safety and effectiveness of these interventions. To learn more about the active clinical trials for the Neurovascular Division, check out our page here: .

Gainesville is a vibrant city in Alachua County and serves as the cultural, educational and commercial center for the North Central Florida region. The city is known for its nature parks, sporting events, museums, mild winters and warm summers. Being centrally located makes Gainesville easily situated for day trips to beaches along the Atlantic Ocean and Gulf of Mexico, and to theme parks including Disney World, and other cities including Orlando and Tampa. To learn more about what Gainesville has to offer: .

Expected Salary:

$50,000 - $60,000 annually; commensurate with education and experience.

Minimum Requirements:

Bachelor's degree in an appropriate area and two years of relevant experience; or an equivalent combination of education and experience.

Preferred Qualifications:
  • 2 years or more of human subject research
  • Knowledge of NIH and FDA procedures
  • Knowledge of state and federal regulations regarding clinical research
  • knowledge of accepted procedures and ethical, confidential practices
  • Proficient in the use of personal computer software, including Microsoft Office
  • Ability to interpret complex guidelines
  • Ability to communicate effectively and to meet deadlines as demanded by the position
Special Instructions to Applicants:

In order to be considered, you must upload your cover letter and resume. Please include 3 to 5 professional references within the application.

The University of Florida is an equal opportunity institution dedicated to building a broadly diverse and inclusive faculty and staff. We are committed to non-discrimination with respect to race, creed, color, religion, age, disability, sex, sexual orientation, gender identity and expression, marital status, national origin, political opinions or affiliations, genetic information and veteran status in all aspects of employment including recruitment, hiring, promotions, transfers, discipline, terminations, wage and salary administration, benefits, and training. Searches are conducted in accordance with Florida's Sunshine Law.

If an accommodation due to disability is needed in order to apply for this position, please call (352) 392-2477 or the Florida Relay System at (800) 955-8771 (TDD).

This is a time limited position.

This requisition has been reposted. Previous applicants are still under consideration and need not apply.

Application must be submitted by 11:55 p.m. (ET) of the posting end date.

Health Assessment Required: Yes

Get job alerts

Create a job alert and receive personalized job recommendations straight to your inbox.

Create alert

Similar jobs