It's More Than a Career, It's a Mission.

Our people are the foundation of our success. By joining our growing team at Sarah Cannon Research Institute (SCRI), a subsidiary of McKesson, you will have the opportunity to become part of one of the largest community-based cancer programs to advance oncology treatments and improve outcomes for cancer patients across the globe. We look for mission-driven candidates who have a desire to advance the fight against cancer and make a difference in the lives of patients diagnosed with cancer every day.

Our Mission

People who live with cancer - those who work to prevent it, fight it, and survive it - are at the heart of every decision we make. Bringing the most innovative medical minds together with the most passionate caregivers in their communities, we are transforming care and personalizing treatment. Through clinical excellence and cutting-edge research, SCRI is redefining cancer care around the world.

As the Regional Director of Oncology Operations you are responsible for operational oversight and collaborative support of research sites in the Denver Market to ensure site goals are achieved while maintaining a high level of financial and quality performance.

• You will provide direction and operational support for the oncology research sites in the Denver Market.

• You will assist in developing and executing SCRI internal and external strategies.

• You will assess organizational processes associated with trial execution and identify ways to improve and streamline internal procedures.

• You will manage and direct the efforts of managers and recommend colleague actions including but not limited to, hiring, performance management, scheduling and work assignments, disciplinary actions, promotions, and transfers.

• You will oversee Managers and work with the central support teams to facilitate study start up, track and trends of enrolment, and provide additional support and education when needed.

• You will collaborate with Blood Cancer and Early Phase Leaders to ensure efficiency in specialty areas.

• You will problem solve clinical situations along with research program members as they arise.

• You will oversee and assist in the creation, development, and execution of SOPs and WIs.

• You will assist in development and tracking of quarterly goals for each site as well as provide proactive and creative recommendations on how to meet goals and handle identified deviations.

• You will collaborate with the quality department to support research activities at each site

• You will identify opportunities and develop action plans as necessary to increase patient accrual.

• You will create and support strategic and tactical plans for site growth

• You will lead the development, implementation, and evaluation of programs to promote the recruitment, retention and continuing education of oncology research managers and staff.

• You will work closely with site, sponsor/CRO monitors, and study managers to quantify the quality and timeliness of study data

• You will represent the company vision at the sites.

• You will work with the sites on individual site goals, financial performance, quality assurance, oversight and patient enrollment.

• You will ensure collaborative oversight of research site operations.

• You will assist with the process of on-boarding and training new research sites.

• You will assess available research resources and facilitate those resources within each site

• You will assist with continuing education and training to investigators and research staff.

• You will build and maintain strong relationships with site leaders, facility leaders, and site physicians to ensure ongoing success and meet with physicians and administrators as needed to assess performance of site.

• You will proactively manage standard of care or conflict of interest issues

• You will communicate to all stakeholders performance standards and expectations

You should have for this position:

• At least three years of experience managing people

• At least three years of experience working in a clinical setting

• At least three years of experience working in research

• At least three years of experience working in oncology

• A Bachelor's Degree is required and Master's Degree is preferred

• Knowledge of Clinical Research Process

• General Knowledge of Research Regulatory and Quality Assurance Guidelines

• Critical thinking and problem resolution abilities

• Independent work ethic

• Ability to travel independently to collaborate with external sites

Our Base Pay Range for this position

$140,300 - $180,000

We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.