Director of Site Services

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 Director of Site Services, you are responsible for the overall clinical operations and development of Sarah Cannon oncology sites. This includesstudy operations, program development, and trial management. You will work closely with the administrative and physician leadership at the sites as well as the Sarah Cannon physician leaders.

• You will oversee the oncology Sites working closely with the Site Manager

• You will problem solve clinical situations along with the Site staff and Site Manager as they arise

• You will assist in developing and executing Sarah Cannon internal and external strategies

• You will provide oversight, leadership and direction in the management of trials

• You will provide operational oversight and direction to the execution of trials

• You will assess quality of data and performance of clinical trials and develop action plans to address performance gaps

• You will monitor patient accrual rates and implement action plans for sites with accrual issues

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

• You will meet with strategic site's administrators and physicians as needed to ensure contracted services are being provided by Program Development, Regulatory, Budgets/Contracts and QA staff

• You will keep executive and management team abreast of issues, progress, and risks related to trial operations

• You will develop, implement and evaluate programs to promote the recruitment, retention and continuing education of the non-oncology research staff

• You will plan and facilitate meetings and committees to address clinical research issues

• You will be responsible for ensuring the integrity of data/information, providing recommendations for corrective action when necessary

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

• You will assess and work with Sites to ensure compliance

• You will assist in development and tracking of quarterly goals for each Site

• You will work closely with monitors, sponsors and Sites to ensure quality study data

• You will meet with physicians and administrators as needed to assess performance of site

• You will monitor patient enrollment at sites through weekly reports

• You will make visits to the oncology sites

You should have for this position:

• A bachelor's degree is required

• At least three years of experience in oncology

• At least three years of experience in a research setting

• At least three years of management experience

• Research Certification (ACRP or CCRP) preferred

Interested candidates should submit their application through https://www.scri.com/careers/. Applications will be accepted through October 8 2025. Please ensure all required materials are included as outlined in the posting.

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.