How to Apply

A cover letter is required for consideration for this position and should be attached as the first page of your resume. The cover letter should address your specific interest in the position and outline skills and experience that directly relate to this position.

Job Summary

This position will serve as a Research Nurse for the Cancer Center - Clinic Research Group and will be part of the Oncology Clinical Trials Support Unit?s Malignant Hematology Clinical Research Team. The candidate will be responsible for study coordination and nursing responsibilities for patients on clinical trials in the Cancer Center. This position utilizes critical thinking skills to recognize and solve patient/participant problems, utilizes the nursing process and nursing standards to prevent or manage actual/potential patient/research participant problems in the Oncology setting, and ensures screening scheduling and coordination of care of research participants is accomplished as written in the research study protocol. The Research Nurse is required to have a working knowledge of clinical trial protocol requirements and good clinical practices as set forth by federal regulations.

The ideal candidate for this role is a highly motivated oncology nurse who wants to be at the forefront of cutting-edge cancer research and plays a pivotal role in advancing innovative therapies while delivering exceptional, patient-centered care.

The Clinical Research Group Research Nurse will be a key driver of clinical trial excellence: blending advanced nursing practice, scientific rigor, and compassionate care to improve outcomes for patients with hematologic malignancies. The Research Nurse will support a diverse portfolio of multi-tumor experimental therapy clinical trials, including Phase 1, first-in-human (FIH), and other early-phase studies, as well as clinical research involving nuclear medicine and novel therapeutic approaches. This role requires strong interpersonal and organizational skills with excellent attention to detail and ability to multitask and work well under time constraints. The candidate will demonstrate a working knowledge of clinical trial design and conduct and excellent computer skills with proficiency in all Microsoft software applications and an electronic medical record. They will participate in the development of research goals and objectives by attending staff meetings, in-service programs, attending appropriate continuing education opportunities, staff development programs, as well as participating in quality improvement initiatives to support implementation of change. This job will involve both outpatient and inpatient research studies and will require morning and occasional evening hours and may provide patient care.

Responsibilities*

Clinical Trial Coordination & Leadership

• Coordinate complex oncology clinical trials in collaboration with investigators, research staff, ancillary services, and clinical teams
• Support the management and implementation of nuclear medicine clinical trials, including novel radiopharmaceutical and experimental therapeutic studies, in collaboration with investigators, nuclear medicine, radiation safety, pharmacy, imaging, and other multidisciplinary teams
• Participate in the development, implementation, and optimization of new workflows and operational processes for nuclear medicine clinical research, ensuring alignment with study protocols, institutional requirements, and applicable regulatory and safety standards
• Identify, screen, consent, and enroll patients in clinical trials
• Ensure accurate scheduling and execution of study visits, procedures, and protocol-specific requirements
• Facilitate research treatment planning by reviewing protocol structure and requirements with the principal investigator and care team
• Maintain full regulatory compliance and uphold Good Clinical Practice (GCP), ICH, and FDA standards; Maintain current PEERS, CITI or NIH Protection of Human Subjects Training Certification

Advanced Clinical Nursing Practice

• Utilize expert critical thinking to assess, anticipate, and manage patient/participant needs
• Conduct toxicity assessments and grade adverse events under investigator direction
• Supervise dose modifications and manage laboratory abnormalities
• Perform protocol-specific procedures including phlebotomy (PK/PD sampling), EKGs, and other study-related interventions
• Order study-specific labs and procedures in accordance with protocol and departmental guidelines
• Utilizes the nursing process and nursing standards to prevent or manage actual/potential patient/research participant problems in the oncology setting.

Patient & Staff Education

• Provide comprehensive education to patients and families regarding clinical trial participation, treatment expectations, and potential side effects
• Develop educational materials and tools (e.g., drug diaries, tracking documents) to support protocol adherence
• Deliver in-services and ongoing education to clinical and research staff

Operational Excellence

• Serve as a liaison between clinical and research teams to streamline processes, troubleshoot challenges, and identify errors or inconsistencies within clinical trial protocols.
• Support the establishment and ongoing refinement of operational workflows for the program?s emerging nuclear medicine clinical research portfolio, including coordination of research-specific patient visits, laboratory assessments, imaging, safety monitoring, and other protocol-required activities
• Collaborate with the Nuclear Medicine team and other multidisciplinary stakeholders to establish clear roles, responsibilities, communication pathways, and standardized processes for the safe and efficient conduct of nuclear medicine clinical trials
• Maintain lab supplies in collaboration with research lab services and data coordinators
• Participate in quality improvement initiatives, study meetings, and research program development
• Provide cross-coverage for research nurses and coordinators as needed

Required Qualifications*

• Educational Requirement: applicant must meet one of the following: Bachelor?s degree in nursing OR an associate degree or diploma in Nursing and a Master?s degree in Nursing
• Current licensure as a Registered Nurse to practice in Michigan
• Three or more years of RN experience in an inpatient setting OR an infusion setting OR an oncology outpatient setting
• 2 yrs of experience in Clinical trials or 2 yrs of experience in Hematology/Oncology

NOTE: In order to be considered for this position the applicant must have met or will have met all the required qualifications prior to the start date of employment.

RESUME REQUIRED (for both internal & external applicants):

You must attach a complete and accurate resume to be fully considered for this position.

Desired Qualifications*

• 1 or more years of experience coordinating clinical trials
• Hematology/Oncology RN experience
• Previous experience with Epic or MiChart
• SOCRA or ACRP certification

What Benefits can you Look Forward to?

Nursing at Michigan offers a competitive salary with excellent benefits!

Salary range for RSAM Registered Nurses $43.10-$67.03/ hour
Evening Shift Differential-$3.00 / hour
Night Shift Differential- $4.00 / hour
Day Shift Weekend Differential- $2.90 / hour
Evening Shift Weekend Differential- $5.90 / hour
Night Shift Weekend Differential- $6.90 / hour
Charge Nurse Differential- $1.00 / hour

The benefit package includes:
Excellent medical, dental and vision coverage
2:1 Match on retirement savings and immediate vesting
Generous Paid Time Off Allowances
Robust Tuition and Certification support programs
Large offering of no cost CEs and professional development for advancement

Nursing Specific Info

Salary & Nursing Framework Level:
This UMPNC RN posting is posted under the Role-Specific Advancement Model (RSAM) as:
CCC- COMPETENT NE.
Actual RSAM LEVEL and salary will be determined at time of hire.
RSAM levels range from CCC-COMPETENT NE to CCC-EXPERT NE TO CCC-MASTERY NE or CCC-Mastery Plus NE.

Required qualifications must be met by the candidate in order to be interviewed and considered for the position. Posting may be filled after the initial 5-day posting period.
Applicants who have left the UMPNC bargaining unit must include on their resume dates of past employment including months and years of service along with effort.
Positions less than 20 hours/week may be combined.

If you have questions regarding this posting or would like assistance with nursing opportunities please contact Nurse Recruitment at (734) 936-5183.

Modes of Work

Positions that are eligible for hybrid or mobile/remote work mode are at the discretion of the hiring department. Work agreements are reviewed annually at a minimum and are subject to change at any time, and for any reason, throughout the course of employment. Learn more about the work modes .

Work Schedule

Hours: 40 hrs., flexibility required.

Shift: Day shift & occasional evening shift, hours will vary; Monday thru Friday, with the possibility of weekends and holidays

All new employees are expected to float in times of low census.

Union Affiliation

This position is covered under the collective bargaining agreement between the U-M and the Michigan Nurses Association and the U-M Professional Nurse Council union, which contains and settles all matters with respect to wages, benefits, hours and other terms and conditions of employment.

Job Detail

Job Opening ID

282743

Working Title

CLINICAL CARE COORDINATOR: Ambulatory Care Services (Rogel Cancer Center Research Nurse)

Job Title

CLIN CARE COORD COMPETENT-NE

Work Location

Ann Arbor Campus

Ann Arbor, MI

Modes of Work

Onsite

Full/Part Time

Full-Time

Regular/Temporary

Regular

FLSA Status

Nonexempt

Organizational Group

Medical School

Department

MM O-CTSU Stdy Coordinatr Clin

Posting Begin/End Date

9/04/2026 - 9/18/2026

Career Interest

Nursing- All Nursing
Nursing- Ambulatory Care and Clinics
Nursing- Oncology
Nursing- Research