Sr. Clinical Data Manager for i3 Statprobe - Lexington, KY

UnitedHealth Group is an innovative leader in the health and well-being industry, serving more than 55 million Americans. Through our family of companies, we contribute outstanding clinical insight with consumer-friendly services and advanced technology to help people achieve optimal health.i3 Statprobe focuses exclusively on providing the pharmaceutical and biotechnology industries with comprehensive, integrated data service solutions that include data capture, summary, analysis, and reporting for clinical trials across all phases of research. The company demonstrates leadership and innovation by leveraging world-class process design and six-sigma quality, affording clients the ability to maximize efficiencies and exceed customer expectations. As a UnitedHealth Group company, i3 Statprobe is part of a worldwide health care service organization that uses innovation, integrity and commitment to prepare for the future - and you can prepare for yours with us. It's a rare combination for success that only a career with i3 Statprobe can provide.  i3 Statprobe currently has an immediate need for a Sr. Clinical Data Manager to work in our Lexington, KY office.  The Sr. Clinical Data Manager leads data management activities for projects involving multiple and/or complex clinical studies, including global studies.They are able to work without close supervision and can coordinate the activities of other junior staff members. Responsibilities: Assumes overall responsibility for the successful execution of the clinical data management projects assigned to them Reviews and approves all required study documentation Performs any data management activities related to projects, as needed May act as Team Leader for data management projects Provides leadership and supervises data management staff assigned to work on their projects, including Clinical Data Coordinators and Clinical Data Associates Monitors the progress of all data management activities for the project to ensure that project timelines are met Monitors the quality of all data management activities for the project Monitors the data management process for the project to ensure that work is proceeding in an efficient manner Serves as data management contact with Sponsor managing client expectations, noting and responding to out-of-scope work Some business development work may be required, such as input to proposals and client presentations Some line management activities may be required Work effectively with international peers and sponsors, as neededQualifications: BS degree in life or health science, or equivalent education and experience A minimum of five years clinical data management skills in a CRO or pharmaceutical setting Previous clinical data management project leadership experience Diversity creates a healthier atmosphere: an equal opportunity employer. M/F/D/V.