Research Nurse - GI Medical Oncology - MD Anderson
Houston, TX
About the Job
The mission of The University of Texas M. D. Anderson Cancer Center is to eliminate cancer in Texas, the nation, and the world through outstanding programs that integrate patient care, research and prevention, and through education for undergraduate and graduate students, trainees, professionals, employees and the public.
SUMMARY
The primary purpose of the Research Nurse position is to provide basic assessment for protocol eligibility, clinical data design and management, patient and staff education, coordination of specific protocol treatment (in-patient and/or out-patient).
KEY FUNCTIONS
Assessment: Screens patients for protocol eligibility and participation in clinical trials that may require the analysis of patient data and charts using visual acuity to determine eligibility. These duties may require frequent bending and stooping to access patient data and charts that may weigh up to ten pounds. Specific duties may include: assessing in-patients and/or out-patients for protocol eligibility; identifying patient and family education needs regarding treatment and follow-up on specific clinical trials; identifying nursing staff in-service needs regarding administration and monitoring of patients on specific clinical trials; administering protocol survey to patients.
Intervention: Participates in the coordination and monitoring of patient treatment in clinical trials. Specific duties may include: scheduling tests before, during, and after treatment; administering investigational and non-investigational medications as required by the protocol; obtaining pharmacology and other required laboratory specimens for research purposes; monitoring patient responses during treatment on clinical trial and performing general follow-up as required by protocol; teaching patient and family about administration and side effects of medication; in-servicing nursing and technical staff on the management of patients in specific clinical trials; executing primary research design including double and single blind studies; collecting blood samples for the protocol project; maintaining records in endoscopy database as required by primary investigator.
Evaluation: monitors, and in collaboration with the physician, evaluates patient response to protocol treatment. Specific duties may include: determining tumor response to protocol treatment; grading of toxicities as defined in specific protocols; reporting toxicities and adverse drug reactions to protocol sponsor and Institutional Review Board (IRB); entering required research data into the Protocol Data Management System (PDMS) or case report form; assisting the physician in the evaluation of data collected from specific clinical trials.
EDUCATION
Required:
Graduation from an accredited school of professional nursing.
Preferred:
Bachelor of Science degree in Nursing.
EXPERIENCE
Required:
One year of registered nursing experience.
Preferred:
Two years research nurse experience and oncology registered nurse experience.
LICENSURE / CERTIFICATION
Required:
Current State of Texas Professional Nursing license (RN).
Basic Life Support (BLS) or Cardiopulmonary Resuscitation (CPR) certification.
Preferred:
American Heart Association Basic Life Support (BLS), ACLS (Advanced Cardiac Life Support) or PALS (Pediatric Advanced Life Support) certification as required by patient care area.
It is the policy of The University of Texas MD Anderson Cancer Center to provide equal employment opportunity without regard to race, color, religion, age, national origin, sex, gender, sexual orientation, gender identity/expression, disability, protected veteran status, genetic information, or any other basis protected by institutional policy or by federal, state or local laws unless such distinction is required by law. http://www.mdanderson.org/about-us/legal-and-policy/legal-statements/eeo-affirmative-action.html.
Additional Information
#LI-Hybrid
SUMMARY
The primary purpose of the Research Nurse position is to provide basic assessment for protocol eligibility, clinical data design and management, patient and staff education, coordination of specific protocol treatment (in-patient and/or out-patient).
KEY FUNCTIONS
Assessment: Screens patients for protocol eligibility and participation in clinical trials that may require the analysis of patient data and charts using visual acuity to determine eligibility. These duties may require frequent bending and stooping to access patient data and charts that may weigh up to ten pounds. Specific duties may include: assessing in-patients and/or out-patients for protocol eligibility; identifying patient and family education needs regarding treatment and follow-up on specific clinical trials; identifying nursing staff in-service needs regarding administration and monitoring of patients on specific clinical trials; administering protocol survey to patients.
Intervention: Participates in the coordination and monitoring of patient treatment in clinical trials. Specific duties may include: scheduling tests before, during, and after treatment; administering investigational and non-investigational medications as required by the protocol; obtaining pharmacology and other required laboratory specimens for research purposes; monitoring patient responses during treatment on clinical trial and performing general follow-up as required by protocol; teaching patient and family about administration and side effects of medication; in-servicing nursing and technical staff on the management of patients in specific clinical trials; executing primary research design including double and single blind studies; collecting blood samples for the protocol project; maintaining records in endoscopy database as required by primary investigator.
Evaluation: monitors, and in collaboration with the physician, evaluates patient response to protocol treatment. Specific duties may include: determining tumor response to protocol treatment; grading of toxicities as defined in specific protocols; reporting toxicities and adverse drug reactions to protocol sponsor and Institutional Review Board (IRB); entering required research data into the Protocol Data Management System (PDMS) or case report form; assisting the physician in the evaluation of data collected from specific clinical trials.
EDUCATION
Required:
Graduation from an accredited school of professional nursing.
Preferred:
Bachelor of Science degree in Nursing.
EXPERIENCE
Required:
One year of registered nursing experience.
Preferred:
Two years research nurse experience and oncology registered nurse experience.
LICENSURE / CERTIFICATION
Required:
Current State of Texas Professional Nursing license (RN).
Basic Life Support (BLS) or Cardiopulmonary Resuscitation (CPR) certification.
Preferred:
American Heart Association Basic Life Support (BLS), ACLS (Advanced Cardiac Life Support) or PALS (Pediatric Advanced Life Support) certification as required by patient care area.
It is the policy of The University of Texas MD Anderson Cancer Center to provide equal employment opportunity without regard to race, color, religion, age, national origin, sex, gender, sexual orientation, gender identity/expression, disability, protected veteran status, genetic information, or any other basis protected by institutional policy or by federal, state or local laws unless such distinction is required by law. http://www.mdanderson.org/about-us/legal-and-policy/legal-statements/eeo-affirmative-action.html.
Additional Information
- Requisition ID: 170766
- Employment Status: Full-Time
- Employee Status: Regular
- Work Week: Days
- Minimum Salary: US Dollar (USD) 70,500
- Midpoint Salary: US Dollar (USD) 91,500
- Maximum Salary : US Dollar (USD) 116,500
- FLSA: exempt and not eligible for overtime pay
- Fund Type: Soft
- Work Location: Hybrid Onsite/Remote
- Pivotal Position: Yes
- Referral Bonus Available?: Yes
- Relocation Assistance Available?: Yes
- Science Jobs: No
#LI-Hybrid
Source : MD Anderson
