Senior Associate/Manager - Clinical Trial Digital Solution Delivery

at  Lilly

At Lilly, 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 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. We’re looking for people who are determined to make life better for people around the world.

ABOUT LILLY

At Lilly, 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 39,000 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. We’re looking for people who are determined to make life better for patients around the world.
Eli Lilly Cork, is made up of a talented diverse team of over 1,400 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.
Lilly 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. Inhouse 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.
Come join our team - Be Creative, Be an Innovator, and most of all, Be Yourself!
The Clinical Central Services & Innovation (CCSI) organization is responsible for strategically planning and supplying materials, trial support services and innovative capabilities to support the execution of clinical trials globally for all business units across all phases of development. This group is within the Clinical Capabilities organization and partners across functions within the Clinical Design, Delivery and Analytics (CDDA) and Product Research and Development (PRD) to influence trial design and provide solutions to operationalize these trials and enable asset strategies across the portfolio.

MINIMUM QUALIFICATION REQUIREMENTS:

• Demonstrated skill and experience in managing alliances with outside partners including strong negotiation skills.
• Demonstrated knowledge of drug development processes
• Demonstrated ability to set and implement strategies and plans to improve complex drug development processes and capabilities.
• Demonstrated ability to effectively partner/influence cross functionally to deliver results.
• Strong communication skills
• Proficiency in Excel, Visio, and writing documents in Word.
• Detail oriented and can prioritize work according to timelines.

This job description is intended to provide a general overview of the job requirements at the time it was prepared. The job requirements of any position may change over time and may include additional responsibilities not specifically described in the job description. Consult with your supervision regarding your actual job responsibilities and any related duties that may be required for the position.

Portfolio Delivery

• Provide knowledge and consultation relating to area of expertise.
• Work with the consultant to support collaborations with quality, legal and procurement as needed in accordance with assessments, audits, master service agreements and contracts.
• Implement strategies to grow services, increase vendor capabilities and expedite delivery on the portfolio.
• Ensure collaboration with other functions regarding strategy and process changes.
• Maintain catalogue of capabilities and solutions modes to meet therapeutic area and global needs.

TPO Oversight and Process Improvement

• Participate in the preparation of required TPO oversight documents.
• Contribute and document TPO oversight, and Quality audit and assessment processes, as required.
• Establish performance level metrics with TPO that can be provided on a defined regular basis.
• Collaborate with business partners and TPOs to develop and maintain appropriate capabilities to match business needs.
• Bring domain expertise to functional initiatives.
• Work to improve existing processes and to implement new processes in an efficient manner
• Ability to assess and understand TPO logistic and regulatory gaps in order to mentor and assist in implement global deployment processes.

People Development

• Serve as a domain expert across LRL and all Business Units
• Model the Lilly leadership behaviours.
• Provide coaching within the organization that fosters inclusion and innovation, continuous improvement, and an external awareness and understanding.
• Hold oneself and others accountable while recognizing the critical impact as a team member.