Clinical Research Coord III- Department of Neurology
About The Position
The Clinical Research Office (CRO), in the Office of Research Affairs (ORA), Dean's Administration, College of Medicine, Jacksonville is looking for a Clinical Research Coordinator III. The position will function independently in clinical research settings and will be responsible for the complete coordination of assigned clinical research activities within the Vose Research Laboratory. The CRC will work with patients and research staff in various clinics around the greater Jacksonville area within the UF enterprise. Will have supervisory responsibilities. Effective problem solving, writing and communication skills. Ability to multi-task working as part of a team or independently. This position will be responsible for all aspects of clinical studies including feasibility, start up activities, execution and close out activities. Will be involved in reporting requirements and financial management, as directed. This position will handle complicated multi-center clinical trials and work with faculty to develop strong investigator-initiated clinical studies.
Requirements
- Bachelor's degree in an appropriate area and three years of relevant experience; or an equivalent combination of education and experience.
- Effective problem solving, writing and communication skills.
- Ability to multi-task working as part of a team or independently.
- Will have supervisory responsibilities.
Nice To Haves
- Master’s degree or PhD in an appropriate area and 5 years of experience coordinating or managing scientific research.
- Excellent interpersonal skills and the ability to prioritize and effectively communicate verbally and in writing.
- Coordinates multiple tasks and work independently and productively in a fast paced, deadline-oriented environment.
- Proficiency in data management and superior organization skills.
- Integrity, careful attention to detail.
- Ability to maintain confidentiality, demonstrate professionalism and respect for subjects’ rights and individual needs.
- Willing to learn and maintain skills in accordance with HIPAA regulations and Good Clinical Practice guidelines.
Responsibilities
- Provide guidance to the research team on the clinical study, budget development, and oversee the implementation and complete execution of the study.
- Assist in the identification of funding opportunities, organizing appropriate collaborations across UF enterprise and externally.
- Involved in reporting requirements, financial management of clinical research studies.
- Working with the principal investigator to identify new opportunities and partnerships with industry and other sponsors with the objective to grow the clinical research portfolio.
- Serve as highly experienced research coordinator and resource for clinical trials and other clinical research projects within the Vose Research Laboratory.
- Conduct study visits for multiple study protocols.
- Coordinate and implement enrollment, study visits and follow-up procedures to collect data from patient charts, medical records, interviews, questionnaires, and other sources.
- Coordinate day to day activities and ensure the compliance of specific research studies.
- Perform blood draws as needed at various time points in clinical trials.
- Assess and report patient reactions to clinical staff and PI.
- Perform vitals, collect specimens, and provide patient care per study protocol.
- Manage tests, procedures, and equipment per protocol requirements.
- Process blood samples in the biomedical and ship biospecimens to the appropriate site.
- Other activities as directed by Principal Investigator, Alicia Vose, PhD.
Stand Out From the Crowd
Upload your resume and get instant feedback on how well it matches this job.
What This Job Offers
Job Type
Full-time
Career Level
Mid Level
