Clinical Research Coord II

Responsible for daily operations of assigned research studies/clinical trials run by the Department of Neurology. The predominant research focus for this position will be studies pertaining to stroke. Specific research coordination skills include creation of source documents, proficient understanding of good clinical practice concepts in terms of documentation, data entry, proper consenting procedures, regulatory oversight, ability to communicate research objectives to patient population, creation of recruitment materials, knowledge of data entry platforms, ability to navigate a research protocol and understand primary outcomes.

Responsible for administrative aspects of all investigator research, industry sponsored trials and device clinical trials; and assists investigators with meeting requirements of external regulatory bodies. Maintains data and filing system of completed ongoing, and pending research protocols. Ensures all required regulatory documentation is completed and submitted as appropriate for all research/clinical trial activity. 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. 

Provides expertise and advice to faculty and the department regarding the design of investigator-initiated research. Provides sources of grant funding through federal, state and private sector organizations/agencies for investigator-initiated research. Trains investigators, fellows and staff regarding the research design, regulatory requirements, and methodology process.

45,000-55,000

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

2 years or more of clinical trials experience.

Excellent interpersonal and communication skills including written and verbal expression, with ability to communicate effectively with lay people and medical professionals. Clarity and comprehensibility of speech in English is essential due to patient facing duties.

Comfortable working with vulnerable patient population with terminal illnesses.

Advanced knowledge of accepted procedures and ethical, confidential practices.

Demonstrates ability to problem-solve; to manage multiple priorities; to be reliable.

Possess strong organizational and time management skills; adhere to study deadlines.

Proven ability to work as part of a team, as well as independently.

Knowledge of NIH and FDA Procedures.

Knowledge of state and federal regulations regarding clinical research.   

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

This is a time limited position.

The University of Florida is 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.