- Lilly (Indianapolis, IN)
- …who are determined to make life better for people around the world. The Associate Director of QC Environmental Monitoring is responsible for the oversight of ... and isolators (eg, viable monitoring - active and passive, non -viable monitoring, personnel monitoring). + Demonstrated technical competency (method understanding)… more
- Lilly (Indianapolis, IN)
- …has become a critical element of setting and executing our strategy. The Associate Director , Competitive Analytics, will influence the broader R&D strategy by ... time pressure. + Skilled in searching out information from both traditional and non -traditional sources, all within the guidelines of our policy. Ability to work… more
- Takeda Pharmaceuticals (Boston, MA)
- …company to inspire you and empower you to shine? Join us as the Associate Director , Software Architect - AI/ML based in Cambridge, MA. **_GOALS_** _:_ ... multiagent orchestration to solve R&D challenges (eg knowledge extraction, medical writing, drug design, clinical trial optimization, etc. ). + Define and document… more
- Organon & Co. (Plymouth Meeting, PA)
- …part of the Commercial Analytics & Insights group and support the US market. The Associate Director will serve as the analytics lead for a designated business ... + Perform in-depth analysis of customer-level engagement data (personal and non -personal) to inform brand opportunities and choices. + Recommend customer engagement… more
- ThermoFisher Scientific (Greenville, NC)
- …development and implementation for foundational (US, EU, CH, DE, AU) and non -US/Central EU markets. + Oversees regulatory review and approval of promotional and ... non -promotional materials to ensure global compliance. + Manages global...quality control, FDA-508 compliance, and annual reporting requirements (US drug listing and NDC assignments). + Coordinate impact assessments… more
- Lilly (Indianapolis, IN)
- …continuous operations across two shifts and therefore, this role will require non -standard work hours, and some work on weekends and holidays. Appropriate ... adjustments in benefits will be provided for employees working non -standard hours where applicable. Qualified candidates must be legally authorized to be employed in… more
- Bristol Myers Squibb (Princeton, NJ)
- …joining our diverse team! As the Product Manager for the Clinical Data Ecosystem within Global Drug Development (GDD) IT at BMS, you will be part of the Drug ... Feasibility, and Real-World Evidence. **Key Responsibilities:** + Collaborate with Global Drug Development (GDD), Global Biometric & Data Science (GBDS) & Enterprise… more
- Gilead Sciences, Inc. (Foster City, CA)
- …projects and teams with responsibilities related to clinical trials or other drug development activities + Familiar with the practice of recording and monitoring ... ICH) and related industry standards and trends + Through knowledge of the drug development process, including all key functions involved in the various stages of… more
- AbbVie (North Chicago, IL)
- …through own efforts and those of her/his staff (if appropriate) for drug development and life-cycle management strategies for assigned projects; for the design, ... validity of study results. Be able to explain statistical concepts to non -statisticians. + Review identified or anticipated technical or data related issues arising… more
- Truist (Charlotte, NC)
- …policies and procedures to effectively manage the risk of GAAP non -compliance by reflecting new accounting pronouncements or guidance, improving clarity or ... you will also learn more about the specific benefits available for any non -temporary position for which you apply, based on full-time or part-time status, position,… more