Bachelors degree in an appropriate area and two years of relevant experience; or an equivalent combination of education and experience.
Job Description:
Research Coordination
Coordinate clinical research studies and clinical trials in compliance with Good Clinical Practice (GCP) standards and other regulatory and legal requirements.
Screen and assist with the identification of research participants.
Obtain informed consent from study participants.
Schedule clinic visits and required testing for research participants.
Assist regulatory and research administration teams with preparation and managementof IRB submissions.
Create and maintain organized research study files and regulatory documentation.
Develop and manage research databases.
Perform accurate data entry and maintain study records.
Self-monitor and self-audit responsibilities.
Assist in the maintenance of .
Develop case report forms (CRFs).
Trains junior coordinators and delegates (with supervisor approval) as appropriate.
Clinical Data Collection and Outcomes Reporting
Collect and manage patient-reported outcomes (PROMs) and quality assurance data.
Track clinical outcomes for spine center programs and research projects.
Analyze data and prepare reports to measure program performance and effectiveness.
Develop and maintain dashboards and reporting tools to display outcomes data.
Serve as liaison for data-related projects between the clinic referral teams hospital partners and other relevant teams.
Develop tools and processes to support quality control and institutional data tracking.
Administrative Support
Support the Research Director and Spine Center leadership with data reporting and special projects.
Schedule and facilitate Comprehensive Spine Center meetings and assist with preparation of monthly meeting agendas and meeting coordination.
Coordinate student and volunteer shadowing opportunities.
Assist with drafting reports presentations manuscripts and program documents.
Expected Salary:
$61350-$69700
Required Qualifications:
Bachelors degree in an appropriate area and two years of relevant experience; or an equivalent combination of education and experience.
Preferred:
Experience using Epic and/or OnCore
Prior experience coordinating clinical research studies in a clinical setting preferably in orthopedics or spine
Familiarity with spine conditions and procedures (e.g. spinal fusion disc herniation spinal stenosis)
Experience with IRB submissions regulatory documentation and maintainingstudy regulatory binders
Experience with electronic data capture systems (e.g. REDCap or Medidata Rave)
Experience with patient recruitment screening and informed consent for clinical trials
Clinical research certification (e.g. CCRC through the Association of Clinical Research Professionals or CRC through the Society of Clinical Research Associates) preferred
Special Instructions to Applicants:
For consideration please complete an application and include a cover letter resume and the names and email addresses of three to five references.
The University of Florida is an Equal Employment Opportunity Employer.
Application must be submitted by 11:55 p.m. (ET) of the posting end date.
Health Assessment Required:
Yes
Required Experience:
IC
Classification Title:Clinical Research Coordinator IIClassification Minimum Requirements:Bachelors degree in an appropriate area and two years of relevant experience; or an equivalent combination of education and experience.Job Description:Research CoordinationCoordinate clinical research studies an...
Classification Title:
Clinical Research Coordinator II
Classification Minimum Requirements:
Bachelors degree in an appropriate area and two years of relevant experience; or an equivalent combination of education and experience.
Job Description:
Research Coordination
Coordinate clinical research studies and clinical trials in compliance with Good Clinical Practice (GCP) standards and other regulatory and legal requirements.
Screen and assist with the identification of research participants.
Obtain informed consent from study participants.
Schedule clinic visits and required testing for research participants.
Assist regulatory and research administration teams with preparation and managementof IRB submissions.
Create and maintain organized research study files and regulatory documentation.
Develop and manage research databases.
Perform accurate data entry and maintain study records.
Self-monitor and self-audit responsibilities.
Assist in the maintenance of .
Develop case report forms (CRFs).
Trains junior coordinators and delegates (with supervisor approval) as appropriate.
Clinical Data Collection and Outcomes Reporting
Collect and manage patient-reported outcomes (PROMs) and quality assurance data.
Track clinical outcomes for spine center programs and research projects.
Analyze data and prepare reports to measure program performance and effectiveness.
Develop and maintain dashboards and reporting tools to display outcomes data.
Serve as liaison for data-related projects between the clinic referral teams hospital partners and other relevant teams.
Develop tools and processes to support quality control and institutional data tracking.
Administrative Support
Support the Research Director and Spine Center leadership with data reporting and special projects.
Schedule and facilitate Comprehensive Spine Center meetings and assist with preparation of monthly meeting agendas and meeting coordination.
Coordinate student and volunteer shadowing opportunities.
Assist with drafting reports presentations manuscripts and program documents.
Expected Salary:
$61350-$69700
Required Qualifications:
Bachelors degree in an appropriate area and two years of relevant experience; or an equivalent combination of education and experience.
Preferred:
Experience using Epic and/or OnCore
Prior experience coordinating clinical research studies in a clinical setting preferably in orthopedics or spine
Familiarity with spine conditions and procedures (e.g. spinal fusion disc herniation spinal stenosis)
Experience with IRB submissions regulatory documentation and maintainingstudy regulatory binders
Experience with electronic data capture systems (e.g. REDCap or Medidata Rave)
Experience with patient recruitment screening and informed consent for clinical trials
Clinical research certification (e.g. CCRC through the Association of Clinical Research Professionals or CRC through the Society of Clinical Research Associates) preferred
Special Instructions to Applicants:
For consideration please complete an application and include a cover letter resume and the names and email addresses of three to five references.
The University of Florida is an Equal Employment Opportunity Employer.
Application must be submitted by 11:55 p.m. (ET) of the posting end date.
Job Location:
Monthly Salary:
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