About this opportunity
PRISM Vision Group lists this Research Nurse Supervisor opportunity in st paul, Minnesota. Review the employer’s description below for duties, qualifications and application requirements.
Job description
Join Minnesota Oncology
Are you ready to take the next step in your professional journey? At Minnesota Oncology, we believe that our people are our greatest asset, and we are committed to fostering a diverse and inclusive workplace where everyone can thrive. We are constantly on the lookout for talented individuals who are passionate, driven, and eager to make a difference.
Come join this dynamic team who is passionate about providing exceptional care to our patients.
Why Work for Us?
We offer a competitive benefits package that includes:
Medical
Dental
Vision
Free Life Insurance
Generous Paid Time Off (PTO) Plan
Free Short-term and Long-term Disability Coverage
401k plan with company contribution
Wellness program that rewards your healthy lifestyle
Tuition Reimbursement
Employee Assistance Program and Discount Program to some of your favorite retailers
Free Parking
Career Growth and Development
Supportive Team and Resources
Responsibilities
Supervises the clinical research staff members in accordance with USON SOP and ICH GCP guidelines. Responsible for ensuring at the administrative level that all research activities are coordinated with affected departments within the practice. Coaches and develops staff. Collaborates in the development of research accountability standards and identifies areas for improvement. Ensures site research quality by practicing in compliance with US Oncology Research, Inc. (USOR) Standard Operating Procedures (SOP), principles of Good Clinical Practice (GCP) and applicable federal, state, and local regulations. Supports and adheres to the US Oncology Compliance Program, to include Code of Ethics and Business Standards.
Key Responsibilities
Supervises clinical research staff members in accordance with USOR SOP and ICH GCP guidelines. Responsible for ensuring at the administrative level that all research activities are coordinated with affected departments within the practice.
Coaches and develops staff. Participates in the recruitment, interviewing, hiring, assessing performance, recommending salary changes, and progressive discipline. Enforces adherence to company policies.
Collaborates in the development of research accountability standards, metrics, and reports and identifies areas for improvement. Collaborates with site research leader (SRL), upper management, and staff in the implementation of action plans designed to improve practice research operations and quality assurance functions.
Collaborates with the SRL, physicians of the practice, and other research management in the process of study selection for the research program.
Collaborates with SRL and upper management on the development of research budgets, financial objectives, and accrual targets.
May promote or market research program to the practice, community, and referring physicians.
May coordinate research activities with other (non-USOR) bases or sponsors.
SALARY LEVEL: $95,000-128,000 annually
Qualifications
Minimum Job Qualifications (Knowledge, Skills, & Abilities):
Education/Training –
Associates degree in a clinical or scientific related discipline required
Graduate of an accredited nursing program
Business Experience -
Minimum 5 years clinical nursing experience, preferably in oncology
Supervisory experience preferred, experience in clinical research preferred
If required in state of practice, current licensure as a registered (RN)
Current BCLS or ACLS certification for nurses
SoCRA or ARCP certification preferred
Specialized Knowledge/Skills -
Excellent communication skills
Strong ability to multitask, strong interpersonal skills
Must be able to work in a fast-paced, constantly changing environment
Knowledge and proficiency in all basic computer programs, Windows, Excel, etc.
Special knowledge of GCP and ICH guidelines preferred
Knowledge of medical terminology, nursing assessment, clinical medicine, diagnostic tests, radiology, pathology, pharmacology, hematology, oncology as it relates to clinical trials
Working Conditions
Traditional office environment.
The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Exposure to communicable diseases, toxic substances, ionizing radiation, medical preparations and other conditions common to an oncology/hematology clinic environment.
Physical Requirements (Lifting, standing, etc.) –
Large percent of time performing computer based work is required.
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Requires full range of body motion including handling and lifting patients, manual and finger dexterity, and eye-hand coordination. Requires standing and walking for extensive periods of time. Occasionally lifts and carries items weighing up to 40 lbs. Requires corrected vision and hearing to normal range.
The US Oncology Network is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability or protected veteran status.
Worksite address
st paul, MN, 55130, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.