- Lilly (Indianapolis, IN)
- …determined to make life better for people around the world. The Clinical Trial (CT) Supply Chain Associate Director will provide operational leadership ... performance and speed drug development. **Key Responsibilities** **:** o Deliver improved clinical trial supply chain performance, assess, mitigate risk, and… more
- Lilly (Indianapolis, IN)
- …wage for this position is $118,500 - $173,800 **Position Brand Description:** The Clinical Trial (CT) Manufacturing organization is responsible for the on-time ... delivery of drug product in support of clinical trials (Phase 1 through 4) as well as...technical and operational components of drug product supply. The Associate Director , CT Manufacturing and Operations has… more
- Lilly (Indianapolis, IN)
- …for people around the world. **Purpose:** The Associate Director (AD) Trial Capabilities will provide leadership in clinical trial capabilities in ... contracts, informed consent negotiations, and other regulatory activities for the clinical trial as applicable to achieve regional goals and objectives. The AD… more
- Lilly (Indianapolis, IN)
- …molecule lifecycle. Additionally, this role is responsible for all aspects of global clinical trial operations within the plan, as the single operational point ... ** Clinical Operations:** + Accountable and responsible for oversight of clinical trial operations and delivery of clinical project milestones on time,… more
- Lilly (Indianapolis, IN)
- …at the compound level. The TA Associate Director engages at a trial level with the therapeutic area, clinical design and other appropriate partners to ... for people around the world. **Job Description** The TA Associate Director , Clinical Laboratory Sciences...can be executed by the study team for the trial . Project management at a molecule level including budget,… more
- Lilly (Indianapolis, IN)
- …culture to ensure diverse voices/ideas are considered. + Serves as mentor for clinical development managers, clinical trial project managers and others ... clinical deliverables in support of submissions, inspections, and publications. The Clinical Development Program Lead reports to the Associate Vice President… more
- Merck (Indianapolis, IN)
- …component of decision-making at our company, this position offers an opportunity for the Associate Director to drive pipeline impact across therapy areas. This ... Associate Director will work with scientists within...models, exposure response (ER) models, model-based meta analysis (MBMA), clinical trial simulations (CTS) and disease progression… more
- Merck (Indianapolis, IN)
- …**Quantitative Pharmacology and Pharmacometrics -** **Immune/Oncology** **(QP2-IO)** team in the role of Associate Director QP2-IO team is part of the Global ... of drug development and effective communication skills. As a subject matter expert, the Associate Director within the QP2-IO Group will work closely with teams… more
- Lilly (Indianapolis, IN)
- …accountable for the final delivery of data collection instruments (English/Translations) used in clinical trials. The C/T associate director also provides ... with study development process and ERB submission requirements + Clinical trial experience in a capacity such...trial experience in a capacity such as Data Associate , Study Coordinator, CRA, etc. + Understanding of the… more
- Lilly (Indianapolis, IN)
- …who are determined to make life better for people around the world. The Clinical Trial (CT) manufacturing organization is responsible for the make and release ... of parenteral drug product, supporting the Clinical Supply and Delivery (CSD) organization and their objectives....the Operations (OPS) team of the manufacturing organization. The Associate Director will be expected to anticipate… more
- Lilly (Indianapolis, IN)
- …internal and industry data standards, and ownership for data standards across the clinical trial data flow. This position collaborates with Data Standards ... standards to be used and followed at each stage of the clinical trial dataflow, including terminology, data verification standards, and CRF instructions. +… more
- Lilly (Indianapolis, IN)
- …and mentoring role. - The development, conduct and reporting of corporate/global clinical trial (s) in support of registration and commercialization of potential ... of physicians on the day-to-day medical operations of the trial and will report to the AVP/Medical Director...**Responsibilities:** The - Cardiometabolic Health - Incretin Outcome Trials Clinical Research Physician will play a critical role in… more
- Lilly (Indianapolis, IN)
- …deliver required materials (such as API, drug product formulations, registration stability lots, clinical trial materials, etc) as needed to support a particular ... project. + Resolve issues with the cross-functional project team with TS/MS priorities in mind. + Encourage appropriate risk taking within the team by leading risk assessments and contingency planning at the team level. + Ensure strategic alignment with… more
- Lilly (Indianapolis, IN)
- …internal and external manufacturing, as well as occasional FTZ support for clinical trial development. + **FTZ Structure Establishment:** Lead the establishment ... of new FTZ structures and zones at five new manufacturing sites. + **Stakeholder Collaboration:** Partner with external consultants and internal collaborators, including Manufacturing Strategy, Supply Chain, Finance, Procurement, Tax, and Legal, to structure… more
- Merck (Indianapolis, IN)
- …Regional Director of Medical Affairs (RDMA) (where applicable), US Global Clinical Trial Organization, Global Medical and Scientific Affairs (GMSA) TA leads, ... alignment with organizational priorities. Along with the USMA Field Leaders (Executive Director (ED)/ Associate Vice President (AV)), the SDMA is responsible for… more
- Lilly (Indianapolis, IN)
- … trial data in Clinical Trial Registry activities. Clinical Planning + Communicate and collaborate with Director -Medical and Business Unit Team ... product development activities over the entire spectrum of drug development and clinical trial phases. Specific activities include developing or contributing to… more