Research Nurse II

Position Description :

Every great life-changing discovery begins the same way-with new knowledge. It can change everything, from a single life to the future of entire communities.

That's why academic medicine, and the continuous pursuit of knowledge, is at the center of everything we do at the Medical College of Wisconsin (MCW).

In the role ofa Research Nurse II you will beworking in the Cancer Center.

Purpose

Aid in the conduct of clinical research studies for disease teams within the Cancer Center Clinical Trials Office. Act as a central resource by sharing nursing knowledge with patients and team members to instruct on protocol related therapy and guide them in their decision making related to protocol compliance.

Provide and document complex research observations and perform precise assessments.

Primary Functions

• Support the adult oncology research teams as a clinical resource to provide central patient screening and eligibilty reviews for potential participants in oncology clinical research trials.
• Support the adult oncology research team as a clinical resource as well as potential participants in complex clinical research opportunties.
• Assist in the collection and evaluation of data. Complete all forms required for proper protocol documentation. Enter information into database and other programs including, but not limited to, EPIC Medical Record, OnCore CTMS, Cancer Center ACCESS tool and Florence eBinder.

Maintain and secure patient records.

Under physician direction, maybe asked to perform protocol-specific clinical tasks including patient assessment (i.e. toxicity management, drug compliance, performance status), screening, ordering tests and procedures, collecting specimens, and monitoring responses.

May administer medication or other types of protocol specific intervention.

Identify problems or obstacles in the system / procedures related to implementation of the research protocols and data collection and communicate to the study investigators and clinical teams.

Notify appropriate personnel of any complications or untoward effects of research studies.

• Provide patient and family education. May provide staff education concerning research protocols as required.
• Assist with the development, implementation and monitoring of QI activities. Implement and conduct quality control processes to ensure the highest standards.

Develop clinical review data review plan and edit check specifications. Utilize CTO quality improvement tools & process control to facilitate improvement of systems & processes.

• Assist in the writing and submission of IRB protocols and consent forms when necessary. Assure compliance with all relevant IRB and other regulatory agency requirements.
• Maintain and manage data and data systems supporting research activities. This includes correspondence with IRBs; forms and data entry and cross-checks;

development and maintenance of computerized record systems to track and account for patients participating in research; and systems to assure that research procedures are accurately billed.

Additionally, maintain confidentiality of all patient-related records including written and verbal communications.

Identify problems or obstacles in the system / procedures related to implementation of the research protocols and communicate to the CTO Manager and study investigators.

Notify appropriate personnel of any complications or untoward effects of research studies.

• An active member of the CTO and CTO committees. Facilitate collaboration of multi-disciplinary research study team members along with CTO Team Manager and Principal Investigators to assure continued protocol interest and adherence.
• Assist in development of standard operating procedures and guidelines for the CTO. Work with partner organizations to improve communication and efficiency as needed.
• Assist in training of clinical research staff as applicable.

Preferred Schedule :

8 : 00 to 4 : 30-can vary depending on clinical need

Position Requirements :

Specifications

Minimum Required Education : Bachelor's Degree

Minimum Required Experience : 3 years registered nursing experience in oncology.

Preferred Education : Bachelor of Science in Nursing, or other advanced degree

Preferred Experience : Clinical research nurse experience, oncology preferred

Field : Nursing

Certification : Current Wisconsin RN Licensure. ONS and Certified Clinical Research Coordinator (ACRP) or Certified Clinical Research Professional (SoCRA) preferred.

CITI training within 30 days of hire.

Why MCW?

• Outstanding Healthcare Coverage, including but not limited to Health, Vision, and Dental. Along with Flexible Spending options
• 403B Retirement Package
• Competitive Vacation and Paid Holidays offered
• Tuition Reimbursement
• Paid Parental Leave
• Pet Insurance
• On campus Fitness Facility, offering onsite classes.
• Additional discounted rates on items such as : Select cell phone plans, local fitness facilities, Milwaukee recreation and entertainment etc.

For a full list of positions see : www.mcw.edu / careers

For a brief overview of our benefits see :

Eastern Wisconsin is a vibrant, diverse metropolitan area. MCW is intent on attracting, developing, and retaining a diverse workforce and faculty body that reflects the community we serve.

We value diversity of backgrounds, experience, thought, and perspectives to advance excellence in science and medicine. MCW is a welcoming campus community with a strong culture of collaboration, partnership, and engagement with our surrounding community .

For more information, please visit our institutional website at .

MCW as an Equal Opportunity Employer and Commitment to Non-Discrimination

The Medical College of Wisconsin (MCW) is an Equal Opportunity Employer. We are committed to fostering a diverse community of outstanding faculty, staff, and students, as well as ensuring equal educational opportunity, employment, and access to services, programs, and activities, without regard to an individual's race, color, national origin, religion, age, disability, sex, gender identity / expression, sexual orientation, marital status, pregnancy, predisposing genetic characteristic, or military status.

Employees, students, applicants or other members of the MCW community (including but not limited to vendors, visitors, and guests) may not be subjected to harassment that is prohibited by law or treated adversely or retaliated against based upon a protected characteristic.