About Us
Eli Lilly Cork is a global healthcare leader headquartered in Indianapolis, Indiana. We unite caring with discovery to make life better for people around the world. Our talented diverse team of over 2000 employees across 60 nationalities deliver innovative solutions that add value across various Business Service functions.
Our Commitment to Diversity and Inclusion
We cater to all dimensions ensuring inclusion of all ethnicities, nationalities, cultural backgrounds, generations, sexuality, visible and invisible disabilities, and gender. Our four pillars: EnAble, embRACE, LGBTQ+, and GIN-Gender Inclusion Network promote awareness and create a disability confident culture within Eli Lilly Cork and beyond.
Purpose
The Associate Director, Trial Capabilities, Budgets & Contracts role leads clinical trial capabilities in support of clinical development. This includes leading teams in the execution of clinical trial budgets and contracts activities across EMEA countries/region enabling patient enrolment readiness in the portfolio of clinical trials.
Primary Responsibilities
1. Clinical Trial Leadership
Lead and coordinate the execution of clinical trial budgets and contracts activities across country/region for high priority (Game Changer and Potential Game Changer) and complex trials representing geographical complexity.
Anticipate and mitigate risks and resolve complex and critical risks/issues to enable timely delivery of Trial Capabilities commitments across countries/region with special attention to Payments.
Influence and challenge internal and external factors shaping clinical trial execution.
2. Organizational Leadership
Identify and ensure shared learning across the clinical organization and with other functional groups within CDDA.
Build capabilities in the function through process improvement, tools, and training.
3. People Management and Development
Recruit, develop, and retain an operationally capable workforce skilled and knowledgeable in clinical development.
Develop an organizational culture that fosters inclusion and innovation.
Requirements
* Bachelor's degree preferably in a scientific or health-related field.
Experience in clinical practice, clinical research, or pharmaceutical medicine, and the drug development process.
* At least six (6) years of clinical trial budgets and contracts leadership experience or relevant experience.
Preferred Qualifications
* Deep therapeutic expertise and knowledge of clinical research.
Previous supervisory experience.
Demonstrated leadership behaviors with ability to accept challenges, seek opportunities to remove barriers, lead in areas of uncertainty, and influence without authority.
Working at Lilly
Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form for further assistance.