
Associate Director, Patient Engagement - Data Insights, Costing and CoDesign
- Cork
- Permanent
- Full-time
- Provide strategic, technical and operational direction to a diverse team and ensure that processes for the assigned area(s) of focus (Data Insights, Costing, CoDesign) are well integrated within the appropriate Clinical Design Delivery & Analytics (CDDA) functions.
- Oversee that the team effectively provides value through strategic and technical expertise in the creation of right-sized design strategies, including a successful transition to delivery.
- Ensure cross-functional collaboration to successfully deliver work expectations/deliverables, including, but not limited to, Clinical Capabilities, CDDA, Quality, Tech@Lilly, etc.
- Proactively assess and identify emerging technical needs or potential changes in strategic direction.
- Drive continuous improvement by understanding the needs/challenges of patients/caregivers and investigators and influencing internal change to improve their experiences.
- Lead and influence cross-functional communication and shared learning to ensure a common understanding of experiences, accountabilities, and best practices.
- Drive the adoption of innovative approaches/tactics to enable the successful recruitment and retention of representative patient populations; anticipate issues and proactively mitigate them to ensure the optimised delivery of strategies and goals.
- Engage with industry representatives to understand organisational experiences and best practices; seek opportunities to shape environmental practices.
- Responsible for recruiting, developing and retaining an innovative, clinically focused and operationally capable workforce
- Responsible for building a team culture that is inclusive, representative and fosters innovation.
- Responsible for developing staff who demonstrate expertise in drug development, therapeutic area science, project management, cross-functional engagement, and judgment-based decision making.
- Responsible for establishing and maintaining a flexible staffing strategy to support changing portfolio needs.
- Responsible for facilitating performance management, personnel development, and career development through frequent interactions, coaching, transparent feedback, and escalation of issues as appropriate.
- Responsible for identifying and resolving personnel issues in collaboration with human resources and functional management.
- Responsible for participating in and representing staff in succession planning activities, talent assessment, merit pay, promotion processes, and reward and recognition activities to retain and motivate staff.
- Responsible for ensuring staff compliance with Lilly Corporate, Medical, Regulatory, global standards/procedures, and other internal and external business requirements, including training requirements.
- Bachelor's degree in a scientific, analytical, financial or health-related field
- Minimum 5-8 years’ experience in clinical trials/drug development or broader pharmaceutical industry
- Previous supervisory experience
- Broad understanding of the pharmaceutical drug/device development process
- Strong leadership skills
- Demonstrated critical thinking skills
- Demonstrated ability to take strategic knowledge and effectively influence the direction of daily operations
- Strong interpersonal and excellent communication (written and verbal), organisational and negotiation skills
- Demonstrated ability to influence team members and extended team members
- Values and leverages diversity and inclusion
- Prior experience in managing complex/cross-functional projects
- Experience leading teams through transformational change
- Prior project management experience and/or experience leading multi-disciplinary teams
- Minimal travel required