- Supporting PIs in the development and growth of the research cores currently consisting of biomarker,neuroimaging, clinical cognitive, and data science.
- Building and maintaining professional working relationships across different disciplines within UF Health.
- Implementing procedures and plans to meet the goals of the Program and assigned studies.
- Scheduling and facilitating project meetings.
- Communicating with Department and University faculty and staff and team members, sponsors, and otherexternal constituencies including service delivery professionals.
- Compliance management including maintaining IRB and protocol compliance, storing of regulatorydocumentation and study records according to protocol.
- Documenting adverse events and providing information to appropriate Principal Investigators (PI)
- Maintaining the PeCAN research handbook outlining research engagement guidelines, availableresources, and database access.
- Managing digital and hard copy clock collection in the pre surgical setting; problem solving digital clockpens and files issues.
- Digitally scoring preoperative digital metrics affiliated with grant funded investigations.
- Coordinating junior faculty and fellow trainees who are engaged in PeCAN related research, includingmeeting coordination, overseeing research productivity, and funding needs, assisting with completion ofIRB required documents, and participant recruitment process.
- Ensuring personnel at study sites understand and comply with standard operation procedures (SOPs) asoutlined by PIs.
- Managing extremely large databases (one with N>16,000) and supporting other junior PIs building similardatabases as part of the PeCAN pilot program.
- Overseeing the collection of data from multiple sites.
- Compiling and organizing data for data integration and analyses.
- Running basic statistical analyses with a biostatistician guidance.
- Coordinating with Data Analyst within the Department of Anesthesiology for the data repository andhospital/medical records related data associated with grant related projects.
- Preparing reports, summaries, and protocols.
- Supporting PIs in the documentation of multicenter studies.
- Managing pre and post award budget in collaboration with PIs.
- Serving as a credible resource regarding IRB regulatory processes.
- Supporting staff and junior PIs with writing IRB regulatory documents and consent forms.
- Assisting PIs and junior researchers with study design and execution in collaboration with PeCANstatisticians.
- Collaborating with staff and PIs to problem solve as issues arise to ensure successful study completions.
- Assisting in grant writing and journal application submissions for PeCAN collaborated grants.
- Assisting PIs and junior faculty with writing and editing posters and articles for publications in peerreviewed journals and conferences.
- Serving as a custodian over financial compensation distribution to research participants.
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Clinical Research Coord II - Gainesville, United States - University of Florida
Description
Clinical Research Coord IIJob no:
Work type: Staff Full-
Time Location:
Main Campus (Gainesville, FL)
Categories:
Allied Health, Grant or
Research Administration Department:
MD-ANESTHESIOLOGY-GENERAL
Classification Title:
Clinical Research Coord II
Job Description:
This position serves as the Clinical Research Coordinator II for the Perioperative Cognitive Anesthesia Network(PeCAN) Alzheimer's Disease and Related Disorders Program and other assigned studies.
Responsible forday-to-day management of research projects, assisting with grant submissions, managing large datasets ina clinical research environment, statistical analyses with supervision, and coordinating data acquisition in aclinical environment using digital technology.
Duties Include:
Facilitate research project operations and day-to-day management of research projects for thePerioperative Cognitive Anesthesia Network (PeCAN) Alzheimer's Disease and Related DisordersProgram and other assigned studies.
Responsible for coordinating database development and data maintenance through REDCap, as wellas access to large existing perioperative neuroimaging, neuropsychology, and biomarker databases.
Thisincludes:
Grant Administration:
Expected Salary:
$48,000 - $50,112
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:
Applicant must have experience with cognitive testing in a fast paced preoperative environment.
Knowledge of digital technology for cognitive testing is needed.
Applicant must help write grants to study cognitive decline in older adults. Must be proficient in SPSS and/orSAS for statistical analyses.
Applicant must understand the importance of cognitive decline in older adults as it relates to the rising issueof public health and be able to create promotional material about this rising issue to relay to the public andrelevant medical professionals.
Applicant is ideally bilingual to extend research reach to diverse patient groups.Special Instructions to Applicants:
In order to be considered you must upload your cover letter and resume.
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.
This is a time limited position.Application must be submitted by 11:55 p.m. (ET) of the posting end date.
Health Assessment Required:
NoAdvertised: 08 May 2024 Eastern Daylight Time Applications close: 14 May 2024 Eastern Daylight Time