Job ID: 376384
About the Job
Coordinate all aspects of multiple oncology and/or hematology clinical trials for solid tumor malignancies. Clinical trials include Phase I-II trials under locally held INDs, as well as Phase II/III industry sponsored trials. This requires multidisciplinary skills directed towards clinical patient management and safety, protocol administration, providing education and training to research staff, clinical staff, medical providers, patients and their families.
Incumbent at this level knows fundamental concepts, practices and procedures. Identifies and resolves readily identifiable problems.
Utilizes the nursing process and standards to perform protocol-specific procedures, prevent or manage research subjects' participation in all clinical research settings.
Administers medications and treatments, as defined by study protocol.
Conducts, coordinates and serves as a resource for various aspects of clinical trials from start-up to closeout according to study protocols.
-Contributes to study start-up activities, including site initiation visits, document template creation, study staff training, and clinical in-services.
-Patient recruitment, screening, consent, enrollment and necessary registrations.
-Provides education to staff, subjects and families about protocols, treatment, possible side effects and complications.
-Performs study data collection and entry; collect enrollment and treatment data, using charts, correspondence, electronic medical records and personal communications with other healthcare workers.
-Assists research team with routine quality control checks.
-Assist with study close-out activities as directed.
Completes and submits required documentation to regulatory agencies. Identifies and assesses defined adverse events and reports to appropriate parties. May be done in collaboration with a Regulatory Specialist.
Participates in production of research publications or presentation of research data.
*These factors are used to determine the complexity of a clinical trial:
Level of Disease, Level of Acuity, Independence
Level of Thinking/Knowledge Level, Level of Supervision
Qualifications
All required qualifications must be documented on application materials.
REQUIRED:
- BS degree in Nursing, current licensure to practice as a Registered Nurse in the State of Minnesota, AND at least 4 years of professional nursing experience or advanced degree plus at least two years of relevant experience, or a combination of education and relevant work experience to equal at least eight years.
- Must have pediatric or adult oncology/hematology clinical experience or clinical research experience.
- Experience with Word, Outlook, and web-based systems for tracking activities, calendaring, and retrieving/updating information.
- Demonstrated/documented ability to work independently, make decisions, problem solve and prioritize the simultaneous management of multiple clinical studies.
-Possess excellent communication skills; verbal and written.
- Flexibility with work schedule to accommodate subject visits.
*Proof of non-active tuberculosis and immunization for or resistance to measles, mumps, rubella, Hepatitis B, pertussis and influenza are required.
PREFERRED:
- Experience with pediatric or adult oncology/hematology clinical trials.
- Experience with EPIC
- Familiarity with the University of Minnesota, University of Minnesota Medical Center Fairview hospital and clinics
- Phlebotomy skills
- Ability to integrate clinical care with clinical research to meet the needs of the patient.
- Experience with Oncore or equivalent clinical trials management system
About the Department
The Masonic Cancer Center (MCC) is an NCI-designated Comprehensive Cancer Center dedicated to cancer research, education, and patient care for the citizens of Minnesota and the surrounding region. Since the time of the first award in 1997, there has been consistent growth of the membership and research base, enabling our center to further advance our knowledge and enhance care for our catchment area. We are driven to be the choice academic healthcare environment for patients, clinicians, scientists and students who seek exceptional, compassionate, precision cancer therapy; innovative clinical trials and prevention programs; cutting-edge research opportunities; and outstanding advanced education.
Pay and Benefits
Pay Range: $85,000 - $110,000; depending on education/qualifications/experience
Time Appointment: 100% Appointment
Position Type: Civil-Service & Non-Faculty Labor Represented Staff
Please visit the Office of Human Resources website for more information regarding benefit eligibility.
The University offers a comprehensive benefits package that includes:
About the Job
Coordinate all aspects of multiple oncology and/or hematology clinical trials for solid tumor malignancies. Clinical trials include Phase I-II trials under locally held INDs, as well as Phase II/III industry sponsored trials. This requires multidisciplinary skills directed towards clinical patient management and safety, protocol administration, providing education and training to research staff, clinical staff, medical providers, patients and their families.
Incumbent at this level knows fundamental concepts, practices and procedures. Identifies and resolves readily identifiable problems.
Utilizes the nursing process and standards to perform protocol-specific procedures, prevent or manage research subjects' participation in all clinical research settings.
Administers medications and treatments, as defined by study protocol.
Conducts, coordinates and serves as a resource for various aspects of clinical trials from start-up to closeout according to study protocols.
-Contributes to study start-up activities, including site initiation visits, document template creation, study staff training, and clinical in-services.
-Patient recruitment, screening, consent, enrollment and necessary registrations.
-Provides education to staff, subjects and families about protocols, treatment, possible side effects and complications.
-Performs study data collection and entry; collect enrollment and treatment data, using charts, correspondence, electronic medical records and personal communications with other healthcare workers.
-Assists research team with routine quality control checks.
-Assist with study close-out activities as directed.
Completes and submits required documentation to regulatory agencies. Identifies and assesses defined adverse events and reports to appropriate parties. May be done in collaboration with a Regulatory Specialist.
Participates in production of research publications or presentation of research data.
*These factors are used to determine the complexity of a clinical trial:
Level of Disease, Level of Acuity, Independence
Level of Thinking/Knowledge Level, Level of Supervision
Qualifications
All required qualifications must be documented on application materials.
REQUIRED:
- BS degree in Nursing, current licensure to practice as a Registered Nurse in the State of Minnesota, AND at least 4 years of professional nursing experience or advanced degree plus at least two years of relevant experience, or a combination of education and relevant work experience to equal at least eight years.
- Must have pediatric or adult oncology/hematology clinical experience or clinical research experience.
- Experience with Word, Outlook, and web-based systems for tracking activities, calendaring, and retrieving/updating information.
- Demonstrated/documented ability to work independently, make decisions, problem solve and prioritize the simultaneous management of multiple clinical studies.
-Possess excellent communication skills; verbal and written.
- Flexibility with work schedule to accommodate subject visits.
*Proof of non-active tuberculosis and immunization for or resistance to measles, mumps, rubella, Hepatitis B, pertussis and influenza are required.
PREFERRED:
- Experience with pediatric or adult oncology/hematology clinical trials.
- Experience with EPIC
- Familiarity with the University of Minnesota, University of Minnesota Medical Center Fairview hospital and clinics
- Phlebotomy skills
- Ability to integrate clinical care with clinical research to meet the needs of the patient.
- Experience with Oncore or equivalent clinical trials management system
About the Department
The Masonic Cancer Center (MCC) is an NCI-designated Comprehensive Cancer Center dedicated to cancer research, education, and patient care for the citizens of Minnesota and the surrounding region. Since the time of the first award in 1997, there has been consistent growth of the membership and research base, enabling our center to further advance our knowledge and enhance care for our catchment area. We are driven to be the choice academic healthcare environment for patients, clinicians, scientists and students who seek exceptional, compassionate, precision cancer therapy; innovative clinical trials and prevention programs; cutting-edge research opportunities; and outstanding advanced education.
Pay and Benefits
Pay Range: $85,000 - $110,000; depending on education/qualifications/experience
Time Appointment: 100% Appointment
Position Type: Civil-Service & Non-Faculty Labor Represented Staff
Please visit the Office of Human Resources website for more information regarding benefit eligibility.
The University offers a comprehensive benefits package that includes:
- Competitive wages, paid holidays, and generous time off
- Continuous learning opportunities through professional training and degree-seeking programs supported by the Regents Tuition Benefit Program