TRAVEL - Research RN - Non Therapeutic Chippenham (868) M-F 7A-4P
Apply NowCompany: Chippenham Hospital
Location: Richmond, VA 23223
Description:
Details
Client Name
Chippenham Hospital
Job Type
Travel
Offering
Nursing
Profession
RN
Specialty
Clinic
Job ID
30624461
Job Title
TRAVEL - Research RN - Non Therapeutic Chippenham (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: 7A-4P
Guaranteed Hours: Not specified
Experience: Minimum years of experience not specified
License: Required
Certifications: None 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.
- Adhere to the Code of Conduct philosophy and the Mission and Value Statement.
- Complete assigned training requirements by the specified due date.
- Accurately complete study medication order forms and obtain necessary signatures prior to medication administration.
- Perform routine operational activities for multiple research protocols.
- Liaise between site research personnel, industry sponsors, and Supervisors.
- Collaborate with various site departments/teams, including finance and administrative representatives.
- Coordinate protocol schedules from initial submission of feasibility to study closeout.
- Coordinate submission and approval for the Site's Facility Review Committee, if applicable.
- Provide instruction on research protocols to appropriate staff, interpreting test results and study data.
- Assess and document patient findings at each clinic visit while on protocol.
- Document all tasks required by the protocol, including medication forms and vital signs.
- Ensure medications are approved by appropriate designees before treatment initiation or change.
- Accurately calculate and document necessary conversions as per protocol.
- Record all interactions regarding patients enrolled on protocols, including follow-ups and phone calls.
- Schedule follow-up appointments and related procedures according to protocol requirements.
- Complete and submit data requests 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 the appropriate study personnel or manager.
- Timely re-consent patients and appropriately document the process.
Client Details
Address
7101 Jahnke Rd
City
Richmond
State
VA
Zip Code
23225
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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
Chippenham Hospital
Job Type
Travel
Offering
Nursing
Profession
RN
Specialty
Clinic
Job ID
30624461
Job Title
TRAVEL - Research RN - Non Therapeutic Chippenham (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: 7A-4P
Guaranteed Hours: Not specified
Experience: Minimum years of experience not specified
License: Required
Certifications: None 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.
- Adhere to the Code of Conduct philosophy and the Mission and Value Statement.
- Complete assigned training requirements by the specified due date.
- Accurately complete study medication order forms and obtain necessary signatures prior to medication administration.
- Perform routine operational activities for multiple research protocols.
- Liaise between site research personnel, industry sponsors, and Supervisors.
- Collaborate with various site departments/teams, including finance and administrative representatives.
- Coordinate protocol schedules from initial submission of feasibility to study closeout.
- Coordinate submission and approval for the Site's Facility Review Committee, if applicable.
- Provide instruction on research protocols to appropriate staff, interpreting test results and study data.
- Assess and document patient findings at each clinic visit while on protocol.
- Document all tasks required by the protocol, including medication forms and vital signs.
- Ensure medications are approved by appropriate designees before treatment initiation or change.
- Accurately calculate and document necessary conversions as per protocol.
- Record all interactions regarding patients enrolled on protocols, including follow-ups and phone calls.
- Schedule follow-up appointments and related procedures according to protocol requirements.
- Complete and submit data requests 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 the appropriate study personnel or manager.
- Timely re-consent patients and appropriately document the process.
Client Details
Address
7101 Jahnke Rd
City
Richmond
State
VA
Zip Code
23225
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.