Sr. Director - Global Patient Safety PV Systems
Scorpion Therapeutics, Indiana, Pennsylvania, us, 15705
Role Summary
The Senior Director – GPS Safety Data Sciences/PV Systems provides strategic leadership for GPS-wide systems technology, automation and data reporting/analytics. The role collaborates with GPS, Lilly Research Laboratories (LRL) and IT to understand business needs, develop an integrated strategy, and lead capability building and execution, influencing GPS needs across the company. Responsibilities
Own automation, technology, and analytics strategies for GPS and ensure input, influence, and efficient implementation across GPS and related functions. Benchmark automation/process efficiency and data insights efforts within and outside Lilly and apply learnings to GPS operations. Build business technology capabilities and skills to support GPS future state. Liaise with leaders across GPS globally to assess needs, align on solutions, and ensure global consistency. Partner with IT and Quality in developing broad technology strategies for GPS and in ongoing implementation and support of existing systems. Partner with Clinical and Statistics organizations to influence GPS business needs and solutions. Develop strong partnerships with similar functions across the company to leverage learnings, resources, and capabilities. Maintain safety systems to support regulatory compliance and ensure effective training for staff before assuming responsibilities. Understand regulatory and business requirements and proactively adapt policies, procedures, and practices as required. Support external and internal inspections through direct participation and resource coordination. Qualifications
Bachelor’s degree within a health science, information technology field or equivalent experience. 5+ years experience supporting drug development areas (e.g., Safety, Clinical, Project Management, IT, etc.). 2+ years of prior experience in Pharmacovigilance. Experience implementing small and large systems/technology projects. Skills
Demonstrated application of process automation and analytics cross-functionally. Strategic thinking and ability to drive broad change. Robust leadership, interpersonal and management skills. Ability to work in a multicultural virtual global environment. Strong verbal and written communication skills in English. Proficiency with essential computer tools (office suite and internet browsers). Relationship-building and cross-functional collaboration capabilities. Education
Bachelor’s degree as specified in Qualifications. Additional Requirements
Availability to travel when required. Based in Indianapolis, IN (relocation provided); remote work considered with 50%+ travel to Indianapolis and possibly other locations.
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The Senior Director – GPS Safety Data Sciences/PV Systems provides strategic leadership for GPS-wide systems technology, automation and data reporting/analytics. The role collaborates with GPS, Lilly Research Laboratories (LRL) and IT to understand business needs, develop an integrated strategy, and lead capability building and execution, influencing GPS needs across the company. Responsibilities
Own automation, technology, and analytics strategies for GPS and ensure input, influence, and efficient implementation across GPS and related functions. Benchmark automation/process efficiency and data insights efforts within and outside Lilly and apply learnings to GPS operations. Build business technology capabilities and skills to support GPS future state. Liaise with leaders across GPS globally to assess needs, align on solutions, and ensure global consistency. Partner with IT and Quality in developing broad technology strategies for GPS and in ongoing implementation and support of existing systems. Partner with Clinical and Statistics organizations to influence GPS business needs and solutions. Develop strong partnerships with similar functions across the company to leverage learnings, resources, and capabilities. Maintain safety systems to support regulatory compliance and ensure effective training for staff before assuming responsibilities. Understand regulatory and business requirements and proactively adapt policies, procedures, and practices as required. Support external and internal inspections through direct participation and resource coordination. Qualifications
Bachelor’s degree within a health science, information technology field or equivalent experience. 5+ years experience supporting drug development areas (e.g., Safety, Clinical, Project Management, IT, etc.). 2+ years of prior experience in Pharmacovigilance. Experience implementing small and large systems/technology projects. Skills
Demonstrated application of process automation and analytics cross-functionally. Strategic thinking and ability to drive broad change. Robust leadership, interpersonal and management skills. Ability to work in a multicultural virtual global environment. Strong verbal and written communication skills in English. Proficiency with essential computer tools (office suite and internet browsers). Relationship-building and cross-functional collaboration capabilities. Education
Bachelor’s degree as specified in Qualifications. Additional Requirements
Availability to travel when required. Based in Indianapolis, IN (relocation provided); remote work considered with 50%+ travel to Indianapolis and possibly other locations.
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