- Lilly (Indianapolis, IN)
- …better for people around the world. **Main Purpose and Objectives of Position:** The Sr . Director , Clinical Supply Strategy is accountable for partnering ... broader Product Delivery (PD) Organization to speed delivery of clinical trial materials to patients and enable...system (SAP) and communication with key business partners. The Sr . Director provides strategic leadership and technical… more
- Lilly (Indianapolis, IN)
- …us to develop creative solutions to support communities through philanthropy and volunteerism The Clinical Design Sr . Director is the single point of ... given asset or portfolio of assets and the complete trial package. This person will be a key partner...the CDDA to ensure smooth transition to execution. The Sr . Director will integrate clinical … more
- Lilly (Indianapolis, IN)
- …those listed below as well as all other duties as assigned. **_Clinical Plan and Trial Options and Clinical Trial Protocols_** + As the Medical leader ... risks created/discharged, cost, and time). + Represent program and trial design optionality to asset teams and Sr...three (3) years that provides adequate background relevant to clinical trial design of PhII to Phase… more
- Lilly (Indianapolis, IN)
- …to craft viable clinical scenarios. You will work to deliver complete clinical trial packages that enable rapid transition into trial execution. ... + Champion development of the asset strategy and translate to the clinical plan across Clinical Trial Management staff + Demonstrate strong business insight,… more
- IQVIA (Avon, IN)
- …Functionally responsible for all team members throughout the duration of each clinical trial . Assures clear client communication, process documentation, and ... forth by IQVIA Biotech and sponsors. Supports the department director in development of functional training, mentoring, and definition...health-related field with at least five (5) years direct clinical trial experience in a CRO or… more
- Edwards Lifesciences (Indianapolis, IN)
- …will make an impact:** + Act as core team member/lead biostatistician of assigned clinical trial (s) in US and international/global trial + Accountable for ... exceeding the requirements of the Associate Manager Required + Experience in clinical trial design, indication lead + FDA/EMEA/PMDA submission experience +… more
- Takeda Pharmaceuticals (Indianapolis, IN)
- …of the Signal Management and Innovation (SMI) team, you will report to the Senior Director , Head, Signal Management and Innovation (SMI). You will review and ... experience in pharmacovigilance + In depth knowledge and experience of clinical trial methodology, pharmacovigilance regulations, signal detection and… more
- Takeda Pharmaceuticals (Indianapolis, IN)
- …study timelines are achieved. + Perform negotiation and administration of global master clinical trial agreements rate cards. + Support the development of ... of your future at Takeda. Join us as the Senior Site Budgeting Analyst based remotely, reporting to the...study. + Negotiate directly with globally assigned sites master clinical trial agreements rate cards. + Support… more
- Takeda Pharmaceuticals (Indianapolis, IN)
- …of disease, access to targeted patient population, drug landscape, historical/current clinical trial landscape) to influence and inform protocol development, ... of Takeda R&D objectives. **ACCOUNTABILITIES:** + Accountable, in collaboration with Director , Feasibility and/or Sr . Manager, Feasibility for the development… more
- Lilly (Indianapolis, IN)
- …distribution of the medicines needed for clinical trials (CT). As the PRD QA Sr . Director - CT Materials Supply and Centralized Services, you will lead the ... the oversight on quality-related matters and compliance across multiple areas ( Clinical Trial Materials, Wholesalers, Ancillary Supplies, and Chemistry… more