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 includes study 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

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As part of Total Rewards, we are proud to offer a competitive compensation package. This is determined by several factors, including performance, experience and skills, equity, regular job market evaluations, and geographical markets. In addition to base pay, other compensation, such as an annual bonus or long-term incentive opportunities may be offered.