Clinical Research Supervisor

The US Oncology Network; Denver (CO); On-site; USD 80,000 - 105,000; Full time

Benefits offered by this job

Health insurance

Dental insurance

Vision insurance

Wellness program

Health Savings Account (HSA)

Flexible Spending Accounts (FSA)

401(k) retirement plan

Life insurance

Short-term disability

Long-term disability

Employee Assistance Program

PTO

Holiday pay

Tuition reimbursement

Critical illness insurance

Accident insurance

Job summary

Rocky Mountain Cancer Centers in Denver seeks an experienced Oncology Clinical Research Supervisor to lead the daily operations of the clinical research program. You will oversee research staff, ensure regulatory compliance, support study execution, and drive high-quality oncology research to improve patient outcomes.

The role requires strong leadership, a clinical background, and familiarity with GCP and ICH guidelines, with potential involvement in budgeting and program promotion within the

Qualifications

• Associates degree in a clinical or scientific related discipline required.
• Graduate of an accredited nursing program preferred.
• Minimum 5 years clinical nursing experience or scientific related discipline; oncology preferred.
• Supervisory experience preferred; experience in clinical research preferred.
• Knowledge of good clinical practice (GCP) and ICH guidelines preferred.

Responsibilities

• Supervises clinical research staff in accordance with USOR SOP and ICH GCP guidelines.
• Ensures administrative coordination of research activities with affected departments.
• Coaches and develops staff; participates in recruitment, hiring, performance reviews, and salary decisions.
• Ensures adherence to company policies; develops accountability standards, metrics, and reports.
• Collaborates with site research leader, upper management, and staff to improve research operations and quality assurance.
• Assists in study selection, budgeting, and accrual targets; may promote the program to the community.

Education

Associates degree in clinical/scientific discipline

Job description

Overview

Rocky Mountain Cancer Centers, Colorado’s largest and most comprehensive provider of cancer care has an exciting opportunity for a Supervisor of Clinical Research in Denver.

We are seeking an experienced and collaborative Oncology Clinical Research Supervisor to lead the daily operations of our clinical research program. This role is responsible for overseeing research staff, ensuring regulatory compliance, supporting study execution, and advancing high‑quality oncology research that improves patient outcomes.

Salary Range: $80,000.00-$105,000.00

Pay is based on several factors including but not limited to education, work experience, certification, etc. As of the date of this posting, in addition to your salary, RMCC offers the following benefits for this position, subject to eligibility requirements: Health, dental, and vision plans; wellness program; health savings account; flexible spending accounts; 401(k) retirement plan; life insurance, short‑term disability insurance; long‑term disability insurance, Employee Assistance Program; PTO, holiday pay, tuition reimbursement, and employee paid critical illness and accident insurance.

Responsibilities

This is an entry‑level exempt management position-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.

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 preferred Business Experience - Minimum 5 years clinical nursing experience or scientific related discipline required, 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: Environment (Office, warehouse, etc.) – 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. (This description is general in nature and is not intended to be an exhaustive list of all responsibilities. Other duties may be assigned as needed to meet company goals.)

Candidates will be required to show proof of being vaccinated against influenza upon commencing employment. Reasonable accommodations will be considered on a case‑by‑case basis for exemptions to this requirement in accordance with applicable law.

All qualified candidates are required to pass a background check and non‑federal drug test (which excludes marijuana) post offer of employment and prior to hire.