Research Nurse
at Guidehouse
Baltimore, Maryland, USA -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 10 Nov, 2024 | Not Specified | 11 Aug, 2024 | N/A | Good communication skills | No | No |
Required Visa Status:
Citizen | GC |
US Citizen | Student Visa |
H1B | CPT |
OPT | H4 Spouse of H1B |
GC Green Card |
Employment Type:
Full Time | Part Time |
Permanent | Independent - 1099 |
Contract – W2 | C2H Independent |
C2H W2 | Contract – Corp 2 Corp |
Contract to Hire – Corp 2 Corp |
Description:
Job Family:
Nurse (Digital)
Travel Required:
None
Clearance Required:
Ability to Obtain Public Trust
What You Will Do:
We are currently searching for a Research Nurse. This role will independently provide support services to satisfy the clinical and research objectives of the CPN Lab. The primary objective is to provide services and deliverables through performance of clinical support to research participants and research data collection. This is a full-time opportunity located in Baltimore, MD.
- Study drug administration.
- Recruit and follow up with patients for clinical and basic research studies and protocols and provide clinical support to patients participating in protocol.
- Assist research and medical staff interview, screen and evaluate the appropriateness of eligible subjects for participation in the research protocol.
- Manage clinical and research support activities to ensure patient safety and address the clinical needs of the patients.
- Ensure informed consent process and human subjects protection in clinical research and counsel patients regarding the potential risks.
- Participate in direct patient care, in coordination with interdisciplinary team and specific team members to create and communicate a plan of care that balances clinical care needs with research.
- Collaborate with researchers and medical staff to obtain and maintain informed consent and assent and address ethical and legal implication of the research protocol.
- Contribute to all study related IRB and regulatory matters, including all reporting requirements (including deviations, unanticipated problems, adverse events) and report issues and variance promptly to the research team.
- Perform accurate data entry into research database, including the use of standardized scales and assessments.
- Support the general implementation, tracking, data acquisition, collection and reporting of all elements of the protocols.
- Present clinical data in terms which may be understood by the patient, as well as, interpretation at a level which is conversant with other health professional including physicians.
- Collaborate with staff to analyze and evaluate current systems of health care delivery and to identify and implement new practice patterns.
- Participate in clinical practice and research support meetings and develop multidisciplinary performance improvement programs and projects to improve operating procedures, patient care and decrease costs.
Responsibilities:
- Study drug administration.
- Recruit and follow up with patients for clinical and basic research studies and protocols and provide clinical support to patients participating in protocol.
- Assist research and medical staff interview, screen and evaluate the appropriateness of eligible subjects for participation in the research protocol.
- Manage clinical and research support activities to ensure patient safety and address the clinical needs of the patients.
- Ensure informed consent process and human subjects protection in clinical research and counsel patients regarding the potential risks.
- Participate in direct patient care, in coordination with interdisciplinary team and specific team members to create and communicate a plan of care that balances clinical care needs with research.
- Collaborate with researchers and medical staff to obtain and maintain informed consent and assent and address ethical and legal implication of the research protocol.
- Contribute to all study related IRB and regulatory matters, including all reporting requirements (including deviations, unanticipated problems, adverse events) and report issues and variance promptly to the research team.
- Perform accurate data entry into research database, including the use of standardized scales and assessments.
- Support the general implementation, tracking, data acquisition, collection and reporting of all elements of the protocols.
- Present clinical data in terms which may be understood by the patient, as well as, interpretation at a level which is conversant with other health professional including physicians.
- Collaborate with staff to analyze and evaluate current systems of health care delivery and to identify and implement new practice patterns.
- Participate in clinical practice and research support meetings and develop multidisciplinary performance improvement programs and projects to improve operating procedures, patient care and decrease costs
REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Hospital/Health Care
Pharma / Biotech / Healthcare / Medical / R&D
Health Care
Graduate
Lieu of bsn
Proficient
1
Baltimore, MD, USA