- Lilly (Indianapolis, IN)
- …behaviors to develop medicines with safety first and quality always. The Associate Director - Technical Services/Manufacturing Science (TSMS) Visual Inspection ... classification, control strategies, validation strategies, and personnel qualification strategies. The Associate Director - TS/MS Visual Inspection must balance… more
- Lilly (Indianapolis, IN)
- …creative solutions to support communities through philanthropy and volunteerism. The Associate Director Clinical Development, Oncology independently leads the ... on trials with quality, on time, and within scope and budget. The Associate Director consistently demonstrates leadership and influence throughout the trial… more
- Otsuka America Pharmaceutical Inc. (Indianapolis, IN)
- …needs. Remote options may be considered within the US. As an ** Associate Director , Quantitative Pharmacology, Pharmacometrics,** you will support all ... submissions. You will conduct analysis, execution and reporting of **pharmacometrics** studies , while providing input into all phases of drug development including,… more
- Lilly (Indianapolis, IN)
- …to make life better for people around the world. **Position Summary:** The Associate Director , Diagnostic Development will serve as the investigational in vitro ... diagnostic (diagnostic) trial-level expert for global clinical studies where approved diagnostics are needed to support the...+ Own the delivery of appropriate language for global study drug protocols when a diagnostic is included to… more
- Sumitomo Pharma (Indianapolis, IN)
- …seeking a dynamic, highly motivated, and experienced individual for the position of ** Associate Medical Director .** The Associate Medical Director ... a medical safety subject matter expert (SME) on behalf of PVRM for: Study Protocols, Informed Consent Forms (ICF), Safety Management Plans (SMP), Clinical Study… more
- Lilly (Indianapolis, IN)
- …must be capable of using this expertise to enable very complex study designs driven by advanced randomization schemes, complex sourcing strategies, automated ... inventory methodologies, and data flow requirements. **Key Responsibilities:** ** Study Setup process management and oversight** + Partner with medical teams, key… more
- United Therapeutics (Indianapolis, IN)
- …Bachelor's Degree in life sciences, quality, regulatory affairs or a related area of study or 10+ years of biologic or pharma regulatory experience with a Master's ... sciences, quality, regulatory affairs or a related area of study or 7+ years of biologic or pharma regulatory...sciences, quality, regulatory affairs or a related area of study + 8+ years of project or people management… more
- Lilly (Indianapolis, IN)
- …Synthesis and Purification / Small Molecule]_ reports to the API EM Engineering Associate Director and provides technical leadership and expertise in conjunction ... operational incidents. + Peer review documentation of learning points, technical studies , and incident investigations. **Develop and Sustain Process Knowledge** +… more
- ASM Research, An Accenture Federal Services Company (Indianapolis, IN)
- …responsible for online tool development and enhancements and dotted-line reporting to their associate director . Therefore, this role will exist in both circles ... timelines. **Minimum Qualifications** + Bachelor's Degree in a related field of study or equivalent relevant experience. + Certified Tester -- Foundation Level… more
- Grifols Shared Services North America, Inc (South Bend, IN)
- …in more than 110 countries and regions. **Position Overview:** The Medical Director will be responsible for clinical strategy relating to upcoming clinical trials, ... are not limited to the following:** + Design of trials, including study population and eligibility criteria, treatment duration, clinical endpoints, biomarkers, and… more
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