We are looking for people who are determined to make life better for people around the world.
Lilly is a company that believes in the talent of our workforce. One of the best ways to utilize and develop that talent is to use our existing workforce to fill new and/or open positions. If you are looking for a new position within Lilly, you can view and apply to open roles posted in the internal job posting system. You must meet the minimum qualifications outlined in the job description and have/obtain work authorization in the country the position is located in order to be considered. When applying internally for a position, your current supervisor will receive notification that you have applied to the position. We encourage employees to discuss the opportunity with their supervisor prior to applying.
The Clinical Development Trial Lead (CDTL) Associate leads the cross-functional study team in the development and execution of clinical trials and is accountable both regionally and globally to deliver trial(s) with quality, on time, and within scope and budget. The CDTL Associate leverages project management, regional operational knowledge, clinical trial process leadership and expertise, and scientific expertise to drive actions and coordinate efforts to achieve or exceed these trial deliverables.
This role requires the ability to use project management skills, processes and tools to develop and execute local, regional and/or global clinical trials. It also requires partnering with other organizations to coordinate and actively participate in affiliate, site, and investigator training. Additionally, this role involves driving and coordinating local, regional and global, cross-functional study team throughout study implementation, execution, and closure, empowering them to meet the clinical trial deliverables.
Key responsibilities include understanding the scope of work required to complete the clinical trial successfully, developing and tracking global trial enrollment plan, assessing, identifying and monitoring trial-level risks, creating and monitoring the overall budget, and managing relationships and serving as a single point of contact and central owner for trial communication to and from the Clinical Development, CDDA, and Third Party Organization (TPOs).
Bachelor's or University degree (scientific or health-related field preferred) or an advanced degree is required. Additional skills and preferences include applied knowledge of project management methodology, processes and tools, demonstrated ability to work cross-culturally with global colleagues and with TPOs, ability to influence without authority, strong leadership and networking skills, effective and influential communication, self-management, and organizational skills, and flexibility to adjust to altered priorities.
Lilly does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status. #WeAreLilly