TRAVEL - Research RN - Non Therapeutic Johnston Willis (868) M-F 7A-4P
Apply NowCompany: Johnston-Willis Hospital - HP
Location: Richmond, VA 23223
Description:
Details
Client Name
Johnston-Willis Hospital - HP
Job Type
Travel
Offering
Nursing
Profession
RN
Specialty
Clinic
Job ID
30624460
Job Title
TRAVEL - Research RN - Non Therapeutic Johnston Willis (868) M-F 7A-4P
Weekly Pay
$1969.0
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
Job Specialty: Clinical Research
Job Duration: 24 months
Shift: 07:00-16:00
Guaranteed Hours: Not specified
Experience: Minimum of 1 year
License: Registered Nurse (RN)
Certifications: Not specified
Must-Have: Strong understanding of research operations and regulations
Job Description:
- Coordinate multiple research protocols and serve as a liaison with local investigators, clinical staff, and research personnel.
- Practice and adhere to the Code of Conduct philosophy and Mission and Value Statement.
- Complete assigned training requirements by the due date.
- Complete study medication order forms accurately, and ensure they are signed by the physician or appropriate designee 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 departments, including finance, hospital administrative representatives, and the local IRB, if applicable.
- Coordinate protocol schedule of assessments from initial submission of feasibility until study closeout.
- Coordinate submission and approval for the Site's Facility Review Committee, if applicable.
- Provide instruction on research protocols to appropriate staff, including interpretation of test results, observations, and related study data.
- Assess patients and document findings at each clinic visit while on protocol.
- Document all specific tasks required by the protocol (e.g., medication forms, quality of life questionnaires, neuro exams, vital signs sheets, times of lab draws).
- Ensure all medications are approved by the appropriate designee prior to initiating treatment or changing medication regimens.
- Accurately calculate and document BSA, creatinine, STS calculation, or any other conversions needed, per protocol.
- Document interactions regarding patients while they are enrolled in a protocol, including follow-up and survival.
- Ensure follow-up appointments, imaging, or related procedures are scheduled correctly according to protocol requirements.
- Accurately complete all data requests and submit with source documentation within the specified timeframe.
- Generate and track shipments of drugs, devices, 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 a manager.
- Re-consent patients in a timely manner and document the process appropriately.
Client Details
Address
1401 Johnston Willis Dr
City
Richmond
State
VA
Zip Code
23235
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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
Johnston-Willis Hospital - HP
Job Type
Travel
Offering
Nursing
Profession
RN
Specialty
Clinic
Job ID
30624460
Job Title
TRAVEL - Research RN - Non Therapeutic Johnston Willis (868) M-F 7A-4P
Weekly Pay
$1969.0
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
Job Specialty: Clinical Research
Job Duration: 24 months
Shift: 07:00-16:00
Guaranteed Hours: Not specified
Experience: Minimum of 1 year
License: Registered Nurse (RN)
Certifications: Not specified
Must-Have: Strong understanding of research operations and regulations
Job Description:
- Coordinate multiple research protocols and serve as a liaison with local investigators, clinical staff, and research personnel.
- Practice and adhere to the Code of Conduct philosophy and Mission and Value Statement.
- Complete assigned training requirements by the due date.
- Complete study medication order forms accurately, and ensure they are signed by the physician or appropriate designee 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 departments, including finance, hospital administrative representatives, and the local IRB, if applicable.
- Coordinate protocol schedule of assessments from initial submission of feasibility until study closeout.
- Coordinate submission and approval for the Site's Facility Review Committee, if applicable.
- Provide instruction on research protocols to appropriate staff, including interpretation of test results, observations, and related study data.
- Assess patients and document findings at each clinic visit while on protocol.
- Document all specific tasks required by the protocol (e.g., medication forms, quality of life questionnaires, neuro exams, vital signs sheets, times of lab draws).
- Ensure all medications are approved by the appropriate designee prior to initiating treatment or changing medication regimens.
- Accurately calculate and document BSA, creatinine, STS calculation, or any other conversions needed, per protocol.
- Document interactions regarding patients while they are enrolled in a protocol, including follow-up and survival.
- Ensure follow-up appointments, imaging, or related procedures are scheduled correctly according to protocol requirements.
- Accurately complete all data requests and submit with source documentation within the specified timeframe.
- Generate and track shipments of drugs, devices, 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 a manager.
- Re-consent patients in a timely manner and document the process appropriately.
Client Details
Address
1401 Johnston Willis Dr
City
Richmond
State
VA
Zip Code
23235
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.