- Lilly (Indianapolis, IN)
- …quality guidelines needed for successful delivery of the portfolio and clinical trials , the Associate Director / Director possesses the business ... for people around the world. The purpose of the Associate Director / Director Clinical ...regulations and guidelines that apply to the conduct of clinical trials . + Project management, leadership and… more
- Sumitomo Pharma (Indianapolis, IN)
- …of clinical trial methodology, regulatory and compliance requirements governing clinical trials , and experience in development of clinical strategy ... dynamic, highly motivated, and experienced individual for the position of ** Associate ** **Medical Director , Clinical Development - Oncology** . The medical … more
- Lilly (Indianapolis, IN)
- …days remote - a generous relocation package can be included with offer The ** Associate Director - Submission Data Delivery** role leads all aspects of global ... data archiving, data standards, and submission process. **Responsibilities:** The Associate Director -Submission Data Delivery provides technical leadership and… more
- Lilly (Indianapolis, IN)
- …Clinical Delivery is responsible for planning and delivering exploratory and biopharmaceutics clinical trial and submission milestones on time and on budget ... Delivery is responsible for all aspects of global clinical trial operations within the plan, as...regulations and guidelines that apply to the conduct of clinical trials . + Leadership expeinrce + Experience… more
- Bristol Myers Squibb (Indianapolis, IN)
- …and unique perspectives in a supportive culture, promoting global participation in clinical trials , while our shared values of passion, innovation, urgency, ... aims to be the global leader in radiopharmaceuticals. **Job Description** The Assoc. Director , IT Regulatory, Clinical and Enterprise Systems is an integral part… more
- Sumitomo Pharma (Indianapolis, IN)
- … Master Files (TMFs) ready for audits and inspections. Partnering with the Associate Director , Clinical Business Operations, the specialist ensures ... International Council for Harmonization E6(R2). + Fundamental knowledge of the conduct of clinical trials is preferred. + Strong focus on teamwork, attention to… more
- Lilly (Indianapolis, IN)
- …are determined to make life better for people around the world. The Associate Director , Patient Engagement; Engagement & Diversity Delivery is responsible for ... and prompt delivery of Lilly's assets. Technical Leadership + Operationalize clinical trial recruitment and retention strategies for diverse populations… more
- Parexel (Indianapolis, IN)
- …studies, as applicable and/or appropriate for the MD + Providing risk assessment of clinical trials for local sponsorship as needed with the support of the ... expanding our esteemed Medical Sciences Team and seeking an Associate /Medical Director to support the growth of...*Experienced as a Physician in Industry or as a clinical trial investigator with significant clinical… more
- Sumitomo Pharma (Indianapolis, IN)
- …seeking a dynamic, highly motivated, and experienced individual for the position of ** Associate Director , Regulatory Affairs (Oncology).** The Associate ... and working with regulatory templates + Understanding of EU Clinical Trial Regulation and ROW country regulatory... Regulation and ROW country regulatory requirements related to clinical trials The base salary range for… more
- Lilly (Indianapolis, IN)
- …develop innovative solutions to optimize manufacturing processes and increase capacity for clinical trial medicines, while also reducing costs and environmental ... impact. The Associate Director of Materials will lead the...lead the planning and procurement of direct materials supporting clinical supply manufacturing across small molecule, biologics, and peptides… more
- Lilly (Indianapolis, IN)
- …develop innovative solutions to optimize manufacturing processes and increase capacity for clinical trial medicines, while also reducing costs and environmental ... impact. The Associate Director Small Molecule Process Engineering provides...site evolves from a design concept to a GMP clinical trial site. **Key Responsibilities:** + Responsible… more
- Lilly (Indianapolis, IN)
- …develop innovative solutions to optimize manufacturing processes and increase capacity for clinical trial medicines, while also reducing costs and environmental ... impact. The Associate Director - Automation Engineering Analytical Lab, System Administration and Integration, is responsible for the supervision of the process… more
- Lilly (Indianapolis, IN)
- …develop innovative solutions to optimize manufacturing processes and increase capacity for clinical trial medicines, while also reducing costs and environmental ... impact. The Associate Director -Automation Engineering - Control System Hardware, I&C, Projects and Site Support is responsible for the supervision of the… more
- Lilly (Indianapolis, IN)
- …develop innovative solutions to optimize manufacturing processes and increase capacity for clinical trial medicines, while also reducing costs and environmental ... impact. The Associate Director - Biologics Operations is directly responsible for managing the day-to-day manufacturing operations in the Biologics building and… more
- Lilly (Indianapolis, IN)
- …develop innovative solutions to optimize manufacturing processes and increase capacity for clinical trial medicines, while also reducing costs and environmental ... impact. **Position Description:** The Associate Director Operational Readiness is responsible for managing the delivery of operational readiness aspects of the… more
- Otsuka America Pharmaceutical Inc. (Indianapolis, IN)
- The Associate Director of Regulatory Intelligence leads the collection and dissemination of regulatory intelligence and collaborates with SMEs to interpret the ... + Ensure regulatory intelligence specialists have continued access to regulatory, clinical trial , and public domain information resources to identify… more
- Lilly (Indianapolis, IN)
- …develop innovative solutions to optimize manufacturing processes and increase capacity for clinical trial medicines, while also reducing costs and environmental ... impact. The Associate Director - Analytical Quality Assurance ensures that laboratory activities conducted in the Lilly Medicine Foundry and with external… more
- Sumitomo Pharma (Indianapolis, IN)
- …or follow us on LinkedIn. **Job Duties and Responsibilities** + Lead on clinical studies and manage/provide training to team members when needed. + Contribute and ... SAS/SQL and SAS/ODS. + Interact with Statisticians and other clinical teams, perform ad hoc analysis and generate +...quality. + Establish monitoring of data transfers for ongoing trials to identify study conduct or data + undefined… more
- Lilly (Indianapolis, IN)
- …better for people around the world, like data driven drug discovery and connected clinical trials . We hire the best technology professionals from a variety of ... backgrounds, so they can bring an assortment of knowledge, skills, and diverse thinking to deliver innovative solutions in every area of our business. The Global Information and Services Tech team is at the forefront of digitalization to enable and advance the… more
- Lilly (Indianapolis, IN)
- …better for people around the world, like data driven drug discovery and connected clinical trials . We hire the best technology professionals from a variety of ... backgrounds, so they can bring an assortment of knowledge, skills, and diverse thinking to deliver innovative solutions in every area of our business. Lilly is entering an exciting period of growth and we are committed to delivering innovative medicines to… more