Social network you want to login/join with:
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:
159
Posted:
21.01.2025
Expiry Date:
07.03.2025
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
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.
3. Develop and track global trial enrollment plan.
4. Assess, identify and monitor trial-level risks.
5. Create 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. Manage relationships and serve as a single point of contact for trial communication.
8. Apply problem-solving skills to daily issues with cross-functional study team.
9. Identify and assist in developing continuous improvement activities.
10. 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. Clinical trial experience with a strong working knowledge of the clinical research process.
8. Proficiency in use of project management tools and techniques.
9. 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
#J-18808-Ljbffr