TRAVEL- Research RN - Non Therapeutic - Centennial (877) 7A-4P Mon-Fri
Apply NowCompany: TriStar Centennial Medical Center
Location: Nashville, TN 37211
Description:
Details
Client Name
TriStar Centennial Medical Center
Job Type
Travel
Offering
Nursing
Profession
RN
Specialty
Clinic
Job ID
30625209
Job Title
TRAVEL- Research RN - Non Therapeutic - Centennial (877) 7A-4P Mon-Fri
Weekly Pay
$1960.5
Shift Details
Shift
Day - 8x5 - 09AM
Scheduled Hours
40
Job Order Details
Start Date
02/17/2025
End Date
08/04/2025
Duration
24 Week(s)
Job Description
Job Title: Research Nurse
Profession: RN
Specialty: Clinical Research
Duration: 24 months
Shift: 07:00-16:00
Hours per Shift: 9 hours
Experience: Minimum of 1 year
Description:
The Research Nurse is responsible for coordinating multiple research protocols and serving as a liaison with local investigators, clinical staff, and research personnel.
This role is under direct supervision, where the individual will mature in their understanding of research operations and regulations to gain a strong fundamental understanding of human subject research.
Practice and adhere to the Code of Conduct philosophy and Mission and Value Statement.
Complete study medication order forms accurately when needed and ensure physician or appropriate designee signs orders prior to medication administration.
Perform routine operational activities for multiple research protocols.
Liaise between site research personnel, industry sponsors, and Supervisor.
Collaborate closely with various site departments and teams, including finance, relevant hospital administrative representatives, and the local IRB, if applicable.
Coordinate protocol schedule of assessments from initial submission of feasibility until study closeout.
Provide instruction on research protocols to appropriate staff, including interpretation of test results, observations, and related study data to physicians, nurses, and clinical staff.
Assess the patient and document findings at each clinic visit while on protocol.
Document all specific tasks required by the protocol, including medication forms, quality of life questionnaires, neuro exams, and vital signs sheets.
Ensure all medications are approved by the appropriate designee prior to initiating treatment or when changing medication regimens.
Accurately calculate and document necessary protocol conversions such as BSA, creatinine, and STS calculation.
Document any interaction regarding the patient that occurs while the patient is enrolled in a protocol, including follow-up and survival, home health intervention, pharmacies, and patient phone calls.
Ensure follow-up appointments, imaging, or any related procedures are scheduled correctly according to protocol requirements.
Accurately complete all data requests and submit with source documentation within the timeframe specified in the SOP.
Generate and track drug shipments, device shipments, and supplies as needed.
Ensure timely and accurate data completion.
Track and report adverse events, serious adverse events, protocol waivers, deviations, and violations.
Communicate all protocol-related issues to appropriate study personnel or manager.
Re-consent patients in a timely manner and document the process appropriately.
Client Details
Address
2300 Patterson St
City
Nashville
State
TN
Zip Code
37203
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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.
Your mobile info will not be shared with third parties for marketing. Standard messaging and data rates may apply.
Client Name
TriStar Centennial Medical Center
Job Type
Travel
Offering
Nursing
Profession
RN
Specialty
Clinic
Job ID
30625209
Job Title
TRAVEL- Research RN - Non Therapeutic - Centennial (877) 7A-4P Mon-Fri
Weekly Pay
$1960.5
Shift Details
Shift
Day - 8x5 - 09AM
Scheduled Hours
40
Job Order Details
Start Date
02/17/2025
End Date
08/04/2025
Duration
24 Week(s)
Job Description
Job Title: Research Nurse
Profession: RN
Specialty: Clinical Research
Duration: 24 months
Shift: 07:00-16:00
Hours per Shift: 9 hours
Experience: Minimum of 1 year
Description:
The Research Nurse is responsible for coordinating multiple research protocols and serving as a liaison with local investigators, clinical staff, and research personnel.
This role is under direct supervision, where the individual will mature in their understanding of research operations and regulations to gain a strong fundamental understanding of human subject research.
Practice and adhere to the Code of Conduct philosophy and Mission and Value Statement.
Complete study medication order forms accurately when needed and ensure physician or appropriate designee signs orders prior to medication administration.
Perform routine operational activities for multiple research protocols.
Liaise between site research personnel, industry sponsors, and Supervisor.
Collaborate closely with various site departments and teams, including finance, relevant hospital administrative representatives, and the local IRB, if applicable.
Coordinate protocol schedule of assessments from initial submission of feasibility until study closeout.
Provide instruction on research protocols to appropriate staff, including interpretation of test results, observations, and related study data to physicians, nurses, and clinical staff.
Assess the patient and document findings at each clinic visit while on protocol.
Document all specific tasks required by the protocol, including medication forms, quality of life questionnaires, neuro exams, and vital signs sheets.
Ensure all medications are approved by the appropriate designee prior to initiating treatment or when changing medication regimens.
Accurately calculate and document necessary protocol conversions such as BSA, creatinine, and STS calculation.
Document any interaction regarding the patient that occurs while the patient is enrolled in a protocol, including follow-up and survival, home health intervention, pharmacies, and patient phone calls.
Ensure follow-up appointments, imaging, or any related procedures are scheduled correctly according to protocol requirements.
Accurately complete all data requests and submit with source documentation within the timeframe specified in the SOP.
Generate and track drug shipments, device shipments, and supplies as needed.
Ensure timely and accurate data completion.
Track and report adverse events, serious adverse events, protocol waivers, deviations, and violations.
Communicate all protocol-related issues to appropriate study personnel or manager.
Re-consent patients in a timely manner and document the process appropriately.
Client Details
Address
2300 Patterson St
City
Nashville
State
TN
Zip Code
37203
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.