Sr. Director -Trial Management Systems, Clinical Trial Foundations

Eli Lilly and Company • Us, IN

22d • $156,000 - $228,800 • Onsite

About The Position

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. At Lilly, we serve an extraordinary purpose. We make a difference for people around the globe by discovering, developing and delivering medicines that help them live longer, healthier, more active lives. Not only do we deliver breakthrough medications, but you also can count on us to develop creative solutions to support communities through philanthropy and volunteerism. Purpose: Sr Director roles in Clinical Trial Foundations (CTF) focus on capabilities related to: data capture; data delivery; site platforms, monitoring and eTMF; help desk, external focus, management of pilots, Transcelerate; and Business Process Management and OCM/Coms. The Sr Director, CTF is a cross-functional leader and key partner across the business and Tech@Lilly for clinical information management capabilities. They will serve as the clinical system(s) owners and be responsible for the development, implementation and maintenance of the clinical information management and process automation strategy for their area of focus while contributing to the integrated end to end clinical information automation strategy. They will actively engage with internal and external partners on new operating models, capabilities and technologies. The Sr. Director is responsible for collaborating with Process Owners and CDDA leadership in the development of information management strategies and plans, and working with Tech@Lilly leadership and Third Party Organizations (TPO) to drive plan implementation. Primary Responsibilities: 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.

Requirements

• Bachelor’s degree and 5 years of experience in clinical drug development or information flow with expertise in related process, technology and information flows (clinical results and operational) such as IT, Data Sciences, Statistics, Clinical Development, Clinical Project Management and/or Quality/Regulatory.
• Demonstrated ability to set and implement strategies and plans to improve complex drug development processes and capabilities.
• Strong networking, interpersonal and relationship skills, with demonstrated ability to work in teams, across organizational boundaries and achieve results through others.
• Demonstrated credibility and ability to influence peers, management and senior leadership.
• Indianapolis based position.

Nice To Haves

• Previous supervisory experience
• Previous experience with system ownership, implementation of new technology, business process automation
• Proven ability to develop and deliver both strategic and tactical plans
• Knowledge of emerging IT capabilities for clinical research
• Strong problem solving skills
• Flexibility to adjust quickly to changing business priorities

Responsibilities

• System and Capability Ownership and Data Flow
• Gain and maintain strategic alignment for clinical systems with the needs of all user communities and related initiatives.
• Define and manage clinical system and/or capability implementation and scale-up strategy and plan.
• Drive development, use, and quality of clinical systems.
• Serve as clinical system(s) owner.
• Develop, implement, and maintain the clinical information management and process automation strategy for their area of focus while contributing to the integrated end-to-end clinical information automation strategy with business and Tech@Lilly partners.
• Accountable for fiscal responsibility of vendors associated with CTF.
• Actively engages with internal and external business partners to evaluate attributes and risk associated with new operating models, capabilities, and technologies.
• Accountable for the delivery and sustainability of projects in CTF.
• Development and implement integrated communication plans across the organization.
• Maintain visibility across interdependencies across projects.
• Foster collaboration amongst stakeholders and facilitate efficient decision-making.
• Enterprise Leadership and External Focus
• Continually seek and implement improvements to reduce cycle time and decrease work effort resulting in decreased costs that optimize clinical information flow, process and technology.
• In partnership with Tech@Lilly leadership and the business, identify TPO strategies that will enable the CDDA’s clinical information and automation strategy. Provide leadership in the setting of clear business requirements and expectations to enable identification of appropriate technology solutions by the Tech@Lilly organization.
• Lead cross-functional initiatives.
• Within functional and cross-functional teams, exhibit strong business acumen, strong problem-solving skills and agility to adjust to changing business priorities and needs.
• Represent the CTF organization at appropriate internal and external venues.
• Drive shared learning and process expertise between teams within the organization.
• People Management and Partnership
• If applicable, recruit, develop, and retain a scientific, technical and operationally capable workforce skilled and knowledgeable in the overall CTF organization.
• Effectively create and manage an agile organization that continuously meets the needs of a changing portfolio.
• Build an organizational culture that fosters inclusion, innovation, and promotes diversity.
• Partner closely with CDDA leadership, Tech@Lilly and other functions to effectively plan, forecast, and manage the sanctioned projects.

Benefits

• Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance).
• In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).

What This Job Offers

• Job Type: Full-time
• Career Level: Director