The Clinical Development Trial Lead (CDTL) Associate/Sr. Associate/Manager leads the cross-functional study team in the development and execution of clinical trials and is accountable both regionally and globally to deliver trial(s) with quality, on time, and within scope and budget.
Locations (2)
Stamford, Connecticut, United States
Indianapolis, Indiana, United States
Compensation
The anticipated wage for this position is $72,000 - $169,400
Responsibilities
Develop, execute, and deliver local, regional and/or global clinical trials
Monitor the status and make changes as needed to meet trial deliverables
Develop and track global milestones by gaining alignment and integrating inputs across functions and geographies
Assess, identify and monitor trial-level risks and create an integrated trial-level risk mitigation and contingency plan
Understand and monitor cross-functional, trial-level budget components
Requirements
Bachelor’s degree (scientific or health-related field preferred)
Nice to have: Early phase oncology experience
Nice to have: Radioligand Therapy (RLT) experience
Responsible for the supervision of process control engineers and technicians supporting daily operations of the new API manufacturing facility, driving automation evolution toward Industry 4.0 standards and championing GMP compliance.
Compensation
The anticipated wage for this position is $123,000 - $180,400
Responsibilities
Supervise and coach process control team
Drive evolution of automation infrastructure toward Industry 4.0 standards
Champion GMP compliance and data integrity
Lead cross-functional teams to deliver engineering excellence across DCS, PLC, SCADA, batch automation, and HVAC/utilities platforms
Attract, hire, and onboard top talent to the Process Control & Automation Engineering team
Requirements
Bachelor’s degree in Engineering, Chemical or Electrical preferred, Instrumentation & Control, or a closely related technical discipline
The Design Lead (DL) will serve in the following capacity: Be responsible for the overall design delivery for capital project(s).
Compensation
The anticipated wage for this position is $130,500 - $211,200
Responsibilities
Be responsible for the overall design delivery for capital project(s).
Coordinate all design for the Project Manager during all design phases of the project and be responsible in delivering the conceptual design review and basic design review.
Direct the development of the design requirements.
Assist in development and maintenance of the design schedule to meet the project needs.
Participate in the selection of the A/E firms.
Requirements
BS in Engineering (Chemical or Mechanical preferred)
Nice to have: Pharmaceutical process experience
Nice to have: Pharmaceutical project engineer experience
Lead the architecture, deployment, and lifecycle management of enterprise Genetec Security Center environment across multiple sites, owning the technical roadmap for video management (VMS) and access control infrastructure.
Compensation
The anticipated wage for this position is $101,250 - $171,600
Responsibilities
Lead the design, deployment, and ongoing architecture of enterprise-scale Genetec Security Center environments spanning video management (VMS), access control, and integrated security systems across Indianapolis.
Develop and maintain the technical roadmap for the Genetec platform, including server infrastructure sizing, storage architecture, failover/redundancy design, and capacity planning for enterprise growth.
Own platform health and performance: monitor system uptime, troubleshoot complex site issues, and manage patching, upgrades, and firmware lifecycle across servers, edge devices, and appliances.
Design and implement system integrations between Genetec Security Center and third-party systems (identity management, building automation, alarm monitoring, analytics) via SDK, APIs, and native connectors.
Establish and enforce platform standards, configuration baselines, and documentation for site deployments, disaster recovery, and cybersecurity hardening.
Lead and manage litigation, government investigations, and related legal counsel for Lilly’s global operations.
Locations (2)
Indianapolis, Indiana, United States
United States, United States
Compensation
$234,000 - $343,200
Responsibilities
Actively manage litigation, government investigations, and other disputes, directing strategy, selecting and supervising outside counsel, and developing and adhering to reasonable budgets
Lead responses to subpoenas, civil investigative demands, and government inquiries
Update and advise senior leadership on litigation, government investigations, and related matters
Build and maintain relationships with other Legal team members and cross-functional colleagues
Provide practical legal counsel on business initiatives and emerging risks
Analyze industry trends, market share and competitors to identify growth strategies, and prioritize market opportunities and risks.
Lead market and customer research to uncover unmet needs and clinical and economic value drivers; build the market requirements document and prioritize customer segments.
Partner with Product Management and Engineering to shape the product roadmap with new product ideas and improvement recommendations.
Work with Segment and Sales team to analyze the installed base and develop programs that improve customer experience, loyalty and retention.
Develop the NPI business case (incl. target pricing) and the evidence generation plan and budget.
Requirements
Bachelor’s Degree in Marketing, Business Administration or related field
Nice to have: MBA or Master’s degree in Marketing, Business Administration or related field
Nice to have: 8+ years’ experience in marketing, product marketing or related field
PhD-trained AI scientist driving cutting-edge medical imaging and Physical AI research from conception to real-world clinical deployment, shaping AI strategy across imaging, embodied and physics-aware AI, foundation models, and multimodal healthcare systems.
Responsibilities
Define and own the long-term research vision for medical image analysis, Physical AI–enabled imaging systems, foundation models, and multimodal healthcare AI across clinical domains.
Architect and lead the development of state-of-the-art detection, segmentation, classification, reconstruction, and quantitative imaging systems.
Partner deeply with clinicians, radiologists, pathologists, imaging scientists, and regulatory stakeholders to formulate AI problem statements grounded in clinical workflows.
Guide AI solutions through clinical validation, regulatory pathways, and real-world deployment.
Act as a technical mentor and design reviewer for senior scientists, postdocs, and junior researchers.
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