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Associate / Sr. Associate - Clinical Development Trial Lead, Cork
Client:
Lilly
Location:
Cork, Ireland
Job Category:
Other
EU work permit required:
Yes
Job Reference:
396798b7d17e
Job Views:
5
Posted:
23.04.2025
Expiry Date:
07.06.2025
Job 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. 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.
Path/Level: P1
Note: Roles are posted at the lowest level of a band, however, employees should search across all levels of the band to identify all opportunities. Employees hired on banded positions (ex: P1-P3, R1-R2, B1-B3, etc.) transfer at their current level, despite the level indicated on the job posting. For example, if a P2 candidate is selected for a P1-P3 banded position, the candidate will remain a P2 in the new role.
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. Central to all that we do are our talented and motivated professionals, circa 800 of whom are based at our Global Business Solutions centre in Little Island, Cork. There we boast a vibrant workforce made up of over 44 nationalities, speaking over 27 languages.
This, along with the physical expansion of the Little Island campus, means there has never been a more exciting time to be part of the GBS story! Mirroring the existing Island House building, the new Island Hall facility extends our overall capacity to in excess of 1000 employees where Lilly will continue to offer a premium workspace across both buildings, complete with healthcare, pension and life assurance benefits, subsidised canteen, wellbeing facilities, barista, gym, travel subsidies, car-pooling incentives, bike to work scheme, on-site parking and much more.
At the GBS, it’s not just about what we do today, but how we can continuously improve and innovate for present and future operations. We view the development of our highly skilled workforce in much the same way and want to grow your role into an empowering and fulfilling career here at Lilly. Therefore, with the sole purpose of employee progression, weekly Manager 1:1s, a dedicated Learning & Development service and Educational Assistance schemes all await you.
Above all, it’s about being part of an open, welcoming and inclusive culture, one that is further enhanced by the dedication of our committees - Culture Club, Diversity & Inclusion, Sports & Social, Corporate Social Responsibility, Health Safety & Environment and Food.
Responsibilities
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.
Primary Responsibilities:
1. Use project management skills, processes and tools to develop and execute local, regional and/or global clinical trials.
2. Understand the scope of work required to complete the clinical trial successfully. Monitor the status and make changes (per change control process) as needed to meet the deliverables of the trial.
3. Develop and track global trial enrollment plan by gaining alignment and integrating inputs across functions and geographies.
4. Assess, identify and monitor trial-level risks and create one integrated trial-level risk mitigation and contingency plan.
5. Understand the cross-functional, trial-level budget components and monitor the overall budget and assumptions using financial tracking tools.
6. Drive and coordinate local, regional and global, cross-functional study team throughout study implementation, execution, and closure.
7. Be accountable for trial/regional enrollment strategy and execution starting from country allocation through Last Patient Entered Treatment (LPET).
8. Manage relationships and serve as a single point of contact for trial communication.
9. Apply problem-solving skills to daily issues with cross-functional study team.
10. Identify and assist in developing continuous improvement activities based on important trends.
11. Manage TPO qualification process, selection, and oversight.
Basic Qualifications:
Bachelors or University degree (scientific or health-related field preferred) or an advanced degree.
Additional Skills/Preferences:
1. Applied knowledge of project management methodology, processes and tools
2. Demonstrated ability to work cross-culturally with global colleagues and with TPOs
3. Ability to influence without authority
4. Strong leadership and networking skills
5. Effective and influential communication, self-management, and organizational skills
6. Demonstrated ability to manage complex situations through problem-solving
7. Flexibility to adjust to altered priorities
8. Clinical trial experience with a strong working knowledge of the clinical research process.
9. Proficiency in use of project management tools and techniques.
10. 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.
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