Détails du poste

• You will be responsible for the overall research data

• You will oversee clinical trial-related activities completed/performed by the research staff to ensure completeness and accuracy as well as adherence to federal and state guidelines.

• You will problem solve clinical situations along with the research staff and the management team as they arise. 

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

• You will plan, facilitate, and present trial management issues and data status updates at internal and external meetings. 

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

• You will assessquality of data and performance of clinical trials and develops action plans to address performance gaps. 

• You will manage, monitor, and operate within allowed budget. 

• You will review of all program billing outcomes and for working with billing staff and Sarah Cannon in addressing issues impacting financial outcomes and patient billing experience. 

• You will work to ensure successful implementation of the EMR and optimization of clinic processes related to OncoEMR implementation to support clinic outcomes and patient experience. 

• You will promote communication and accountability between staff and physicians. 

• You will monitor billing colleagues and services, provides financial reports and completes financial analysis to determine areas for improvement in financial outcomes. 

• You will maintain competency and enhance professional growth and development through continuing education, conferences, and seminars. 

• You will enhance operational effectiveness, emphasizing cost containment without jeopardizing innovation of quality of care. 

• You will oversee all aspects of patient treatment associated with trial execution, including enrollment, patient consent, lab work, data entry, and drug storage/distribution.

• You will keep the executive team abreast of issues, progress, and risks related to trial operations and the overall clinic and you will meetsfrequently with all investigators. 

• You will assist in developing and executing internal and external strategies. You are responsible for the recruitment, hiring, training, development, and termination of colleagues, as necessary. 

You should have for this role:

• A Bachelor’s Degree is required

• Knowledge of FDA guidelines and GCP.

• Must be able to read, understand and comply with research protocols. 

• Experience using clinical trial databases, electronic data capture, MS Access and MS Excel. 

• At least three years of experience in an oncology setting

It is preferred that you have:

• At least one year of experience supervising or managing others

• At least one year of experience in blood cancer/Bone Marrow Transplant (BMT)

• Research Certification (ACRP or CCRP) preferred