BioSpace
Associate Director– Clinical Trial Foundations
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Associate Director– Clinical Trial Foundations
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BioSpace . 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 work to discover and bring medicines to those in need, improve disease understanding and management, and support communities through philanthropy and volunteerism. We prioritize putting people first and making a positive impact worldwide. Purpose
The Associate Director, Clinical Trial Foundations (CTF), will serve as a subject matter expert for clinical systems and capabilities supporting clinical development. You will define and execute implementation plans to deliver strategies, integrations, and improvements for systems and capabilities. This role involves collaborating with business partners to enable development, implementation, and support of streamlined, compliant systems to support clinical development. You will work closely with external vendors, industry authorities, and related organizations to optimize Lilly’s capabilities for efficient, customer-focused clinical development. The focus will be on working with business, Tech@Lilly, and vendors to implement and enhance automation and processes for user account management of Lilly’s eCOA platforms. Skills in project management, business analysis, automation programming (e.g., Microsoft Power Platform), and data visualization (e.g., Tableau, Looker) are essential. Primary Responsibilities
Understand business strategies, processes, and technology related to clinical development. Serve as a domain expert to ensure data, process, and technology interfaces are optimized across clinical information systems. Support internal audits and external inspections. Project Management
Define, lead, and execute implementation plans, including change management, communications, and training. Develop and monitor success criteria for projects and pilots. Identify and communicate customer needs related to process and technology performance. Lead organizational change, communication, and training initiatives. Provide guidance on forecasting expenses. Identify risks and raise issues appropriately. Lead progress reporting and system metrics to leadership and end users. Partnership
Partner with process owners, leadership, Quality, and Tech@Lilly to ensure effective system usage. Participate in shared learning across teams. Work with vendors to improve customer experience and efficiencies. Minimum Qualifications
Bachelor’s degree in a scientific, technology, or health-related field. At least 3 years of experience in medical, quality, clinical drug development, Tech@Lilly, or clinical information flow. Legally authorized to work in the U.S. (no sponsorship anticipated). Additional Preferences
Experience with clinical development systems and supporting technologies. Knowledge of project management and organizational change. Strong interpersonal, leadership, communication, and business skills. Problem-solving, critical thinking, and conflict resolution abilities. Flexibility and adaptability to change. Knowledge of regulatory and quality standards. Position based in Indianapolis with up to 10% travel.
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Join to apply for the
Associate Director– Clinical Trial Foundations
role at
BioSpace . 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 work to discover and bring medicines to those in need, improve disease understanding and management, and support communities through philanthropy and volunteerism. We prioritize putting people first and making a positive impact worldwide. Purpose
The Associate Director, Clinical Trial Foundations (CTF), will serve as a subject matter expert for clinical systems and capabilities supporting clinical development. You will define and execute implementation plans to deliver strategies, integrations, and improvements for systems and capabilities. This role involves collaborating with business partners to enable development, implementation, and support of streamlined, compliant systems to support clinical development. You will work closely with external vendors, industry authorities, and related organizations to optimize Lilly’s capabilities for efficient, customer-focused clinical development. The focus will be on working with business, Tech@Lilly, and vendors to implement and enhance automation and processes for user account management of Lilly’s eCOA platforms. Skills in project management, business analysis, automation programming (e.g., Microsoft Power Platform), and data visualization (e.g., Tableau, Looker) are essential. Primary Responsibilities
Understand business strategies, processes, and technology related to clinical development. Serve as a domain expert to ensure data, process, and technology interfaces are optimized across clinical information systems. Support internal audits and external inspections. Project Management
Define, lead, and execute implementation plans, including change management, communications, and training. Develop and monitor success criteria for projects and pilots. Identify and communicate customer needs related to process and technology performance. Lead organizational change, communication, and training initiatives. Provide guidance on forecasting expenses. Identify risks and raise issues appropriately. Lead progress reporting and system metrics to leadership and end users. Partnership
Partner with process owners, leadership, Quality, and Tech@Lilly to ensure effective system usage. Participate in shared learning across teams. Work with vendors to improve customer experience and efficiencies. Minimum Qualifications
Bachelor’s degree in a scientific, technology, or health-related field. At least 3 years of experience in medical, quality, clinical drug development, Tech@Lilly, or clinical information flow. Legally authorized to work in the U.S. (no sponsorship anticipated). Additional Preferences
Experience with clinical development systems and supporting technologies. Knowledge of project management and organizational change. Strong interpersonal, leadership, communication, and business skills. Problem-solving, critical thinking, and conflict resolution abilities. Flexibility and adaptability to change. Knowledge of regulatory and quality standards. Position based in Indianapolis with up to 10% travel.
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