Détails du poste

As the Director of Research Site Operations, you are responsible for the overall clinical operations and development of Oncology Research 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 and Operations leaders.

• You will oversee Sites working closely with the Site Manager and Site management team 

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

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

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

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

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

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

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

• You will meet with Site’s administrators and physicians as needed to ensure contracted services are being provided by SCRI Site Support and other key departments such as Therapeutic Development, Regulatory, Budgets/Contracts, IT and QA 

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

• You will support the development, implementation and evaluation of programs to promote the recruitment, retention and continuing education of Site 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 attend and participate in all required key meetings including both internal SCRI and at Site 

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

• You will assess and work with Research 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 be responsible for oversight of Site operations and meet with physicians and administrators as needed to assess performance of Site 

• You will support strategic and tactical plans for oncology site growth and monitor patient enrollment at sites through weekly reports 

• You will represent company vision to site colleagues and affiliated organizations 

• You will communicate to all Research Site's performance standards and expectations and regularly visits Sites 

• You will work with other team members in SCRI Operations department to ensure communication and responsibility are effective among the groups 

• You will collaborates with training and education to ensure continuing education and training to investigators and Research Site staff 

• You will manage OSS colleagues and team contributing tasks as directed 

You should have: 

• Knowledge of Oncology Research clinical organizational policies, standard operating procedures, and systems 

• Knowledge of standard Research Operations 

• At least five years of experience in healthcare, research or other science related fields 

• At least five years of experience in planning, managing or coordinating clinical trial processes 

• Management experience is required 

• Bachelor Degree is required however experience may be a substitute for education 

• Research Credentials (i.e. ACRP, SOCRA) is preferred 

• Nursing or relevant Healthcare Credentials (RN, APRN) is preferred