- Eurofins (Kalamazoo, MI)
- …in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in ... files in accordance with SOPs and regulatory requirements. + Manage data management processes including paper and electronic data capture, overseeing data … more
- Takeda Pharmaceuticals (Cambridge, MA)
- …equivalent plus 7 years of clinical research experience within the pharmaceutical industry, CRO health-related consulting company, or biomedical/clinical ... team on a high priority molecule. At Takeda, we are transforming the pharmaceutical industry through our R&D-driven market leadership and being a values-led company.… more
- Boehringer Ingelheim (Ridgefield, CT)
- …clinical data engineering (CDE) tasks performed by an external partner. Oversee CRO capacities / budget for outsourced trial / project tasks. Develop/test different ... Job Requirements: Bachelor's degree (US or foreign equivalent) in Pharmaceutical Technology, Biomedical Technology, Computer Science, Software Engineering, Computer… more
- Charles River Laboratories (Rockville, MD)
- …week detailed lookaheads and 12-month rolling), GMP preparedness for runs, deviation management , training plans which are executed on by manufacturing, and process ... practices (GDP) incompliance with FDA, EMA, guidelines. **Training and Documentation Management ** * Develop and maintain SOPs, training materials, and documentation… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …equivalent plus 7 years of clinical research experience within the pharmaceutical industry, CRO health-related consulting company, or biomedical/clinical ... in our Cambridge, MA office. At Takeda, we are transforming the pharmaceutical industry through our R&D-driven market leadership and being a values-led company.… more
- Grifols Shared Services North America, Inc (Los Angeles, CA)
- …year of relevant experience in pharmacovigilance, clinical research, or regulatory affairs in a CRO or a pharmaceutical company is usually required. + 2-3 years ... reporting timelines. Responsible for data review, compilation and analysis including management of the integrated safety database. **_Essential Job Duties:_** + … more
- Eurofins (Columbia, MO)
- …in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in ... a supervisor in the laboratory. Responsibilities include: + Responsible for management of the day-to-day laboratory activities. Identifies and recommends training… more
- Charles River Laboratories (Northridge, CA)
- …the highest quality cellular material and services to biotech and pharmaceutical companies and research organizations that are performing innovative research and ... such as Terumo Optia or Trima, which includes set-up, run, quality control , troubleshooting, and routine maintenance with RN oversite. * Performs white blood… more
- Takeda Pharmaceuticals (Boston, MA)
- …equivalent plus 7 years of clinical research experience within the pharmaceutical industry, CRO health-related consulting company, or biomedical/clinical ... Science in our Cambridge office. At Takeda, we are transforming the pharmaceutical industry through our R&D-driven market leadership and being a values-led company.… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …equivalent plus 3 years of clinical research experience within the pharmaceutical industry, CRO health-related consulting company, or biomedical/clinical ... in our Cambridge, MA office. At Takeda, we are transforming the pharmaceutical industry through our R&D-driven market leadership and being a values-led company.… more