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Associate / Sr. Associate - Clinical Development Trial Lead Neuroscience, Cork
Client: Lilly
Location: Cork, Ireland
Job Category: Other
EU work permit required: Yes
Job Reference: 612aa5802110
Job Views: 157
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 Eli Lilly Cork, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our 41,000 employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first.
Eli Lilly Cork is made up of a talented diverse team of over 1,600 employees across 38 nationalities who deliver innovative solutions that add value across a variety of Business Service functions including Finance, Information Technology, Medical, Clinical Trials and more.
Eli Lilly Cork offers a premium workspace across our campus in Little Island, complete with flexible hybrid working options, healthcare, pension and life assurance benefits, subsidised canteen, onsite gym, travel subsidies and on-site parking. In-house People Development services, Educational Assistance, and our ‘Live Your BEST Life’ wellbeing initiatives are just some of the holistic benefits that enhance the career experience for our colleagues.
Eli Lilly Cork is committed to diversity, equity and inclusion (DEI). We cater for all dimensions ensuring inclusion of all ethnicities, nationalities, cultural backgrounds, generations, sexuality, visible and invisible disabilities and gender, with four pillars: EnAble, Age & Culture, LGBTQ+ and GIN-Gender Inclusion Network. EnAble, our pillar for people with disabilities and those that care for them, partners with the Access Lilly initiative to make our physical and digital environment accessible and inclusive for all.
Come join our team - Be Creative, Be an Innovator, and most of all, Be Yourself.
Note: This is a 12 month fixed term contract.
Responsibilities
The Clinical Development Trial Lead (CDTL) 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 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.
* Monitor the status and make changes as needed to meet the deliverables of the trial.
* Develop and track global trial enrollment plan.
* Assess, identify and monitor trial-level risks.
* Create and monitor the overall budget and assumptions using financial tracking tools.
* Partner with other organizations to 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.
* Be accountable for trial/regional enrollment strategy and execution.
* 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 Qualifications:
Bachelors or University degree (scientific or health-related field preferred) or an advanced degree.
Additional Skills/Preferences:
* 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.
* 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.
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