Social network you want to login/join with:Associate / Sr. Associate - Clinical Development Trial Lead, Cork CityClient:LillyLocation:Cork City, IrelandJob Category:OtherEU work permit required:YesJob Reference:396798b7d17eJob Views:190Posted:03.03.2025Expiry Date:17.04.2025Job Description:We’re looking for people who are determined to make life better for people around the world.At Lilly, we believe 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.Path/Level:P1Note: Roles are posted at the lowest level of a band, however, employees should search across all levels of the band to identify all opportunities.At Lilly, we make a difference for people the world over by discovering, developing and delivering medicines that help people live longer, healthier and more active lives.ResponsibilitiesThe 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.Primary Responsibilities:Use project management skills, processes and tools to develop and execute local, regional and/or global clinical trials.Understand the scope of work required to complete the clinical trial successfully.Develop and track global trial enrollment plan.Assess, identify and monitor trial-level risks.Create and monitor the overall budget.Coordinate and actively participate in affiliate, site, and investigator training.Drive and coordinate local, regional and global, cross-functional study team throughout study implementation, execution, and closure.Manage relationships and serve as a single point of contact for trial communication.Apply problem-solving skills to daily issues with cross-functional study team.Identify and assist in developing continuous improvement activities.Manage TPO qualification process, selection, and oversight.Basic QualificationsBachelors or University degree (scientific or health-related field preferred) or an advanced degree.Additional Skills/PreferencesApplied knowledge of project management methodology, processes and tools.Demonstrated ability to work cross-culturally with global colleagues.Ability to influence without authority.Strong leadership and networking skills.Effective and influential communication, self-management, and organizational skills.Demonstrated ability to manage complex situations through problem-solving.Flexibility to adjust to altered priorities.Clinical trial experience with a strong working knowledge of the clinical research process.Proficiency in use of project management tools and techniques.Ability to travel periodically.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
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