| Classification Title: | Clinical Research Coordinator II |
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| Classification Minimum Requirements: | Bachelors degree in an appropriate area and two years of relevant experience; or an equivalent combination of education and experience. |
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| 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.
- Document investigational product (drug/device) accountability.
- 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.
|
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| Expected Salary: | $61350-$69700 |
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| 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
|
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| 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. |
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| Health Assessment Required: | Yes |
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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.
- Document investigational product (drug/device) accountability.
- 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
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