Sr. Director - Clinical Information Management

Eli Lilly • Indianapolis, IN

289d • $151,500 - $222,200

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. Purposes/Overview: Clinical Trial Foundations (CTF) delivers innovative and reliable systems, processes, and information to enable clinical development and speed medicines to patients. The Clinical Design, Delivery & Analytics (CDDA) Information Hub (Info Hub) is a joint business and Tech@Lilly capability with the goal of enabling 'on demand access' to information which has been identified as critical in enabling drug development. The Info Hub focuses on establishing a single, digitized source of information which is accessible and usable across Clinical ensuring quality and timely availability of that information to enable efficiencies across clinical data flow. The Sr Director, Clinical Information Management has leadership accountability for clinical information management and automation capabilities along with ownership of related technologies. The Sr Director is responsible for developing the information management strategy for the information hub and the automation strategy across clinical processes, to achieve cost efficiencies and improved outcomes for clinical development. The Sr Director is responsible for collaborating with Process Owners, System Owners, CDDA functional leadership and Tech@Lilly in the development of information management and automation strategies and drive implementation. The ability to align and integrate this work with other CDDA programs is critical to the success of this role and to CDDA in the long-term enabling on demand information and speeding medicines to patients.

Requirements

• Bachelor's degree.
• Work experience in clinical drug development with expertise in related process, technology and information flows (8 years).
• Management experience (1-3 years).
• Proven ability to develop strategies and translate strategies to plans.
• Technical background, with experiences in system ownership.
• Strong leadership, interpersonal and communication skills.
• Ability to influence broadly across organizations and work effectively across levels.
• Experience in effectively leading organizational change initiatives.
• Established network throughout CDDA.
• Knowledge of emerging IT capabilities used for clinical research.
• Demonstrated track record of successful execution of complex initiatives.

Responsibilities

• Develop, implement, and maintain the clinical information management strategy through effective data governance, stewardship and access processes for key clinical and operational data.
• Deliver on-demand information for highest priority projects enabling digitization, automation and reuse across CDDA and Lilly in partnership with IT, System Owners and Functional Leadership.
• Partner across Lilly to adopt and contribute to enterprise data capabilities related to catalog, storage, access and roles.
• Mature reuse of data to maximize insights and learnings across Lilly.
• In partnership with CDDA functional leadership and Tech@Lilly drive continuous improvement in information and process solutions that enable integrated data and analytics capabilities improving processes resulting in simplification, reduced cycle time and decreased costs.
• Develop, implement, and maintain the clinical automation strategy and associated capabilities.
• Deliver value-based process automation focusing on highest value opportunities in partnership with IT, System Owners, Process Owners and CDDA functional leadership leading to reduction in manual effort.
• Continually seek and implement means of improving processes to simplify, reduce cycle time and decrease work effort resulting in decreased costs.
• Recruit, develop, and retain a scientific and operationally capable workforce skilled in clinical information management and automation, knowledgeable in clinical development processes, and knowledgeable in the application of technology in clinical development.
• Ensure staff receive appropriate training to perform their responsibilities.

Benefits

• 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.
• 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: Senior
• Industry: Chemical Manufacturing
• Education Level: Bachelor's degree