TRAVEL - Research RN -Non Therapeutic - Trinity (889) - 7A-4P Mon-Fri
Apply NowCompany: Brandon Regional Hospital
Location: Brandon, FL 33511
Description:
Details
Client Name
Brandon Regional Hospital
Job Type
Travel
Offering
Nursing
Profession
RN
Specialty
Clinic
Job ID
30620477
Job Title
TRAVEL - Research RN -Non Therapeutic - Trinity (889) - 7A-4P Mon-Fri
Weekly Pay
$1971.58
Shift Details
Shift
Day - 8x5 - 09AM
Scheduled Hours
40
Job Order Details
Start Date
02/18/2025
End Date
08/05/2025
Duration
24 Week(s)
Job Description
Job Title: Research Nurse
Job Specialty: Clinical Research
Job Duration: 24 months
Shift: 07:00-16:00
Guaranteed Hours: Not specified
Experience: Minimum 1 year
License: RN License
Certifications: Not specified
Must-Have: Experience in coordinating research protocols and working with clinical staff and research personnel
Job Description:
- Coordinate multiple research protocols and serve as a liaison with local investigators, clinical staff, and research personnel.
- Develop a fundamental understanding of research operations and regulations to effectively manage human subject research.
- Adhere to the Code of Conduct philosophy and the Mission and Value Statement.
- Complete assigned training requirements punctually.
- Accurately complete study medication order forms and obtain the necessary signatures before medication administration.
- Perform routine operational activities for multiple research protocols.
- Act as a liaison between site research personnel, industry sponsors, and supervisors.
- Collaborate with various site departments/teams, including finance, hospital administrative representatives, and the local IRB.
- Coordinate protocol schedule assessments from initial submission to study closeout.
- Provide and document instructions on research protocols to relevant staff, including interpretation of test results and observations.
- Assess patients and document findings at each clinic visit while on the protocol.
- Document all specific tasks required by the protocol, such as medication forms, quality of life questionnaires, neuro exams, vital signs, lab draw times, etc.
- Ensure that all medications are approved before initiating treatment or when modifying medication regimens.
- Accurately calculate and document necessary conversions as required by the protocol.
- Document interactions regarding patients enrolled on a protocol and ensure correct scheduling of follow-up appointments and procedures.
- Timely and accurately complete and submit data requests with source documentation.
- Manage and track drug, device, and supply shipments as needed.
- Track and report adverse events, serious adverse events, protocol waivers, deviations, and violations.
- Communicate protocol-related issues to the appropriate study personnel or manager.
- Re-consent patients promptly and document the process appropriately.
Client Details
Address
119 Oakfield Dr
City
Brandon
State
FL
Zip Code
33511
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By applying for jobs on this website, you consent to receive daily messages from CYNET about assignments that match your profile. Email or text HELP for more info, or STOP to unsubscribe.
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Client Name
Brandon Regional Hospital
Job Type
Travel
Offering
Nursing
Profession
RN
Specialty
Clinic
Job ID
30620477
Job Title
TRAVEL - Research RN -Non Therapeutic - Trinity (889) - 7A-4P Mon-Fri
Weekly Pay
$1971.58
Shift Details
Shift
Day - 8x5 - 09AM
Scheduled Hours
40
Job Order Details
Start Date
02/18/2025
End Date
08/05/2025
Duration
24 Week(s)
Job Description
Job Title: Research Nurse
Job Specialty: Clinical Research
Job Duration: 24 months
Shift: 07:00-16:00
Guaranteed Hours: Not specified
Experience: Minimum 1 year
License: RN License
Certifications: Not specified
Must-Have: Experience in coordinating research protocols and working with clinical staff and research personnel
Job Description:
- Coordinate multiple research protocols and serve as a liaison with local investigators, clinical staff, and research personnel.
- Develop a fundamental understanding of research operations and regulations to effectively manage human subject research.
- Adhere to the Code of Conduct philosophy and the Mission and Value Statement.
- Complete assigned training requirements punctually.
- Accurately complete study medication order forms and obtain the necessary signatures before medication administration.
- Perform routine operational activities for multiple research protocols.
- Act as a liaison between site research personnel, industry sponsors, and supervisors.
- Collaborate with various site departments/teams, including finance, hospital administrative representatives, and the local IRB.
- Coordinate protocol schedule assessments from initial submission to study closeout.
- Provide and document instructions on research protocols to relevant staff, including interpretation of test results and observations.
- Assess patients and document findings at each clinic visit while on the protocol.
- Document all specific tasks required by the protocol, such as medication forms, quality of life questionnaires, neuro exams, vital signs, lab draw times, etc.
- Ensure that all medications are approved before initiating treatment or when modifying medication regimens.
- Accurately calculate and document necessary conversions as required by the protocol.
- Document interactions regarding patients enrolled on a protocol and ensure correct scheduling of follow-up appointments and procedures.
- Timely and accurately complete and submit data requests with source documentation.
- Manage and track drug, device, and supply shipments as needed.
- Track and report adverse events, serious adverse events, protocol waivers, deviations, and violations.
- Communicate protocol-related issues to the appropriate study personnel or manager.
- Re-consent patients promptly and document the process appropriately.
Client Details
Address
119 Oakfield Dr
City
Brandon
State
FL
Zip Code
33511
Job Board Disclaimer
By applying for jobs on this website, you consent to receive daily messages from CYNET about assignments that match your profile. Email or text HELP for more info, or STOP to unsubscribe.
Your mobile info will not be shared with third parties for marketing. Standard messaging and data rates may apply.