Eli Lilly

This role is responsible for the overall execution, management, and oversight of assigned clinical trials, ensuring adherence to regulatory requirements, Good Clinical Practice (GCP), and company standard operating procedures. It involves leading cross-functional teams to deliver high-quality clinical trial data on time and within budget.

This role focuses on ensuring the quality and compliance of regulatory affairs activities in China for a global healthcare company. Responsibilities include managing regulatory documentation, implementing company SOPs, coordinating local processes, managing RA systems, and providing training. The role also involves collaboration with internal teams and external vendors, supporting technology development, and conducting compliance monitoring and audits. It requires a bachelor's degree, 1-3 years of experience, strong computer skills, and excellent English communication.

This role is an IT Analyst focused on supporting manufacturing operations at Eli Lilly. Responsibilities include managing IT systems, troubleshooting issues, ensuring compliance with GMP and data integrity standards, and leading IT projects. The role requires knowledge of IT infrastructure, business processes, and computer system validation (CSV) within a regulated healthcare environment.

This role is for a Sr. Director/Executive Director of E&C Core Capabilities at Eli Lilly in Shanghai, China. The primary function is to serve as a senior Ethics and Compliance (E&C) Business Partner, providing expert leadership in managing E&C risks and advising on program design, process controls, and risk management. The role involves leading Centers of Excellence for Monitoring & Data Intelligence and Third-Party Organization (TPO) Management, and partnering with business leaders to strengthen controls through risk-based oversight and data-driven insights. The ideal candidate will have over 10 years of experience in ethics and compliance within highly regulated industries, strong analytical capabilities, and the ability to influence senior leaders. Fluency in Mandarin and English is required.

This role is a Master Planner responsible for creating and managing production plans, inventory, and material requirements within SAP for a pharmaceutical manufacturing facility. It involves close collaboration with regulatory, production, and quality departments to ensure compliance and optimize capacity, with a focus on meeting demand while minimizing inventory costs. The role also includes managing change control and reporting on key supply chain metrics.

Senior Manager role in the pharmaceutical industry focused on developing and implementing pricing and reimbursement strategies for the China market. Responsibilities include new product strategy, payer engagement, health economic outcomes research, and cross-functional collaboration.

Manager, Regulatory Delivery Excellence, China Regulatory Affairs at Eli Lilly is responsible for managing regulatory registration processes and submission preparation support, covering clinical trial permit applications through to marketing applications. This role involves developing submission plans, collaborating with cross-functional teams and vendors, managing RIM-related activities, and ensuring compliance with regulations and internal quality systems. The position also requires serving as a Subject Matter Expert for regulatory business processes and the Veeva Vault RIM system, and maintaining data in IT systems.

This role manages laboratory, device, imaging, and other diagnostic support for clinical trials, coordinating vendor activities, partnering with medical staff on protocol development, and ensuring high-quality data. It focuses on clinical trial initiation and execution within the healthcare domain.

This role is for a Senior Warehouse Manager in the pharmaceutical industry, responsible for overseeing all aspects of warehouse operations, including material receipt, storage, dispensing, shipping, inventory control, and compliance with quality, safety, and regulatory requirements (GMP, AEO). The role also involves project management for warehousing initiatives, team leadership, and ensuring a safe work environment. Experience with SAP/PMX and GMP regulations is required.

This role focuses on integrating digital platforms with physical laboratory infrastructure in a healthcare setting. The engineer will design, develop, and validate software solutions, data pipelines, and APIs to connect laboratory systems, automation equipment, and enterprise platforms, ensuring secure, compliant, and scalable operations. The role involves hands-on engineering, business analysis, and collaboration with various teams and vendors to modernize laboratory workflows.

The (Sr.) Medical Education Manager-Onco role at Eli Lilly in Shanghai is responsible for implementing the medical education plan for oncology. This involves identifying educational needs, developing agendas and content, managing speakers, ensuring compliance with policies, and tracking event success. The role also involves engaging with medical societies and TPOs, and ensuring all programs adhere to corporate standards. A Master's degree or above in Medicine with at least 5 years of clinical or industrial experience in Medical Affairs is required. Experience in medical affairs launch and knowledge of adult education principles are preferred.

This role is for a Senior Operator at Eli Lilly's Suzhou manufacturing facility. The primary responsibilities include supporting production, adhering to GMP and SOPs, performing manual and automatic packaging operations, and ensuring HSE compliance. The role requires a high school education, adaptability to shift work, and good vision.

This role is for a (Sr./Principal) TS/MS Engineer focused on commercialization of pharmaceutical products within a regulated healthcare manufacturing environment. Responsibilities include technology transfer, process improvements, post-approval changes, deviation investigation, and supporting regulatory registration. The role requires experience in sterile formulation manufacturing within a cGMP environment.

This role is for a Director of ExploR&D Translational Medicine at Eli Lilly, focusing on the medical strategy and oversight for drug development programs. The incumbent will lead early-phase clinical development, work with external biotech companies and internal experts, and be responsible for medical and safety leadership from candidate selection to proof-of-concept. Key tasks include constructing and executing clinical development plans, integrating scientific concepts, evaluating literature, providing medical leadership for clinical plans, and ensuring compliance with regulations and GCP.

This role is for a Sr. Manager of Regulatory Affairs CMC at Eli Lilly, focusing on new product registrations and life-cycle maintenance from a Chemistry, Manufacturing, and Controls (CMC) perspective. The individual will drive CMC strategy, prepare dossiers, oversee testing, manage queries, and shape the regulatory environment in China. It requires deep technical expertise in CMC drug development and compliance, with a strong understanding of China's regulations and ICH guidelines.

This role is for a Senior Advisor, Clinical Research in Oncology at Eli Lilly, focusing on providing medical expertise for clinical strategy and execution in China. The responsibilities include collaborating on clinical development strategy, interacting with health authorities, developing evidence generation plans, supporting brand commercialization, contributing to payer partnerships, leading medical meetings, and establishing external collaborations. The role requires a Medical Doctor with experience in clinical research or medical advising in the pharmaceutical industry.

This role is a Clinical Program Lead in the ExploR&D organization at Eli Lilly, focusing on managing external collaboration projects in drug discovery and development. The role involves leading cross-functional teams, defining project strategy, managing timelines and budgets, and serving as the primary liaison between Lilly and external biotech collaborators. While the company mentions 'AI/ML tools' as part of its Catalyze360 initiative, the core responsibilities of this specific role are in traditional drug development program management, not in building or directly applying AI/ML models.

This role focuses on designing, developing, and integrating high-throughput analytical automation modules (e.g., PCR, LC, LC/MS) to support chemistry and biology automation workcells. The scientist will partner with external vendors and internal teams to ensure robust data quality, operational reliability, and seamless integration with other systems, ultimately accelerating data generation for drug discovery.

The role focuses on designing, optimizing, and operating automation platforms for RNA therapeutics research, bridging wet-lab biology and automation engineering to create efficient systems for RNA synthesis, purification, quality control, and functional assays within a healthcare setting.

The Country Study Manager (CSM) provides clinical operational expertise for country-level study operations, driving initiation, enrollment targets, quality oversight, and timely delivery of study deliverables. The role also involves contributing to process improvements and change management within ongoing business objectives.

This role is for a Regulatory Affairs Associate Director at Eli Lilly in China, focusing on developing and implementing regulatory strategies to accelerate drug submissions, approvals, and launches. It involves close collaboration with global and local teams, interaction with regulatory authorities, and ensuring compliance with regulations and Lilly's policies. The position requires deep knowledge of drug development, risk management in a regulated environment, and strong negotiation and communication skills in both Chinese and English.

Senior Advisor, Clinical Research at Eli Lilly, focusing on providing medical expertise for clinical strategic planning and execution in drug development and medical affairs within the Chinese market. Responsibilities include collaborating on clinical trial design and conduct, communicating with health authorities, developing evidence generation plans, supporting brand commercialization, and managing medical meetings and publications.

Senior Director for Strategy at Eli Lilly, focusing on external innovation in the China and Asia-Pacific region. The role involves identifying, assessing, and coordinating external search and evaluation efforts for in-licensing opportunities, including agents, technologies, platforms, or targets that align with Lilly's internal R&D pipeline and address unmet patient needs. This includes leading due diligence, partnering with therapeutic area teams, developing relationships within the external pharmaceutical community, and supporting business development initiatives.