What are the responsibilities and job description for the TRAVEL - Research RN - Non Therapeutic Swedish (868) M-F 7A-4P position at HCA HealthONE Swedish?
Details
Client Name
HCA HealthONE Swedish
Job Type
Travel
Offering
Nursing
Profession
Specialty
Clinic
Job ID
30624645
Job Title
TRAVEL - Research RN - Non Therapeutic Swedish (868) M-F 7A-4P
Weekly Pay
1964.45
Shift Details
Shift
Day - 10x4 - 07AM
Scheduled Hours
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 : Knowledge of research operations and regulations
Job Description :
- Coordinate multiple research protocols and serve as a liaison with local investigators, clinical staff, and research personnel.
- Mature in understanding research operations and regulations to achieve a strong fundamental understanding of human subject research.
- Adhere to the Code of Conduct philosophy and Mission and Value Statement.
- Complete training assignments by the due date.
- Accurately complete study medication order forms, obtaining 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, including finance, relevant hospital administrative representatives, and the local IRB, if applicable.
- Coordinate protocol schedules from initial submission of feasibility until study closeout.
- Obtain submission and approval for the Site's Facility Review Committee, if applicable.
- Provide instruction on research protocols to staff, including interpretation of test results and study data to relevant personnel.
- Assess patients and document findings at each clinic visit while on protocol.
- Document specific tasks required by the protocol, such as medication forms, quality of life questionnaires, exams, and vital signs.
- Ensure all medications are approved by appropriate designees before initiating treatment or changing medication regimens.
- Accurately calculate and document BSA, creatinine, STS calculation, or any other conversions needed per protocol.
- Record any interaction with patients while enrolled in a protocol, including follow-up and survival details.
- Ensure follow-up appointments, imaging, or related procedures are scheduled according to protocol requirements.
- Accurately complete and submit all data requests, including queries, within specified timeframes.
- 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 managers.
- Re-consent patients promptly and document processes appropriately.
Client Details
Address
501 E Hampden Ave
City
Englewood
State
Zip Code
80113
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