- Gilead Sciences, Inc. (Foster City, CA)
- …Drive development and implementation of new systems to improve project execution and data management + Lead collaborations with Gilead PDM functions such as Quality ... within the organization + Support regulatory filings by guiding the draft, review , and approval of CMC sections; support associated agency interactions and… more
- Sanofi Group (Richmond, VA)
- …including attendance at relevant symposium, scientific workshops, preceptorships, and review of key journals, and successful completion of internal training ... Sciences/ Nursing + 3-5 years of Industry experience + Experience in biotechnology/ pharmaceutical industry + Prior product launch experience + Ability to present to… more
- Medexus Pharma (CA)
- …2025 Description **Company Bio:** Medexus Pharmaceuticals Inc. is a leading specialty pharmaceutical company with a focus on the therapeutic areas of rheumatology, ... including the provision of guidance on the publication and presentation of clinical data , in accordance with company policies. + Support the creation of Medical… more
- Merck (West Point, PA)
- …molded Device Components, Device Constituents, and Medical Devices used to deliver Pharmaceutical , Biologic, and Vaccine Products. Our team works with a "Safety ... Reliability, and Lifecycle Management). - Lead Periodic Business and Operations Review Meetings (with External Partner). . **Compliance:** Achieve compliance goals… more
- The Cigna Group (Bloomington, MN)
- …+ Meet directly with large and most complex custom clients to review modeling and cultivate relationships with Formulary Decision Makers (ie Pharmacy Directors, ... VP's, etc.). + Evaluate client data , create scenarios, and provide expert formulary modeling and...these programs are accurately represented and in alignment with Pharmaceutical rebate contract. + Analyze the financial impact of… more
- Takeda Pharmaceuticals (Boston, MA)
- …Improvement in our Cambridge office. At Takeda, we are transforming the pharmaceutical industry through our R&D-driven market leadership and being a values-led ... processes. + Design systems that facilitate the automation of repetitive tasks and data analysis to free up valuable scientific resources for critical thinking and… more
- ThermoFisher Scientific (Greenville, NC)
- …sterile injectables and work on problems of moderate scope where analysis of situations or data requires a review of a variety of factors. This colleague follows ... when performing the following duties. A Day in the Life: + Ensure pharmaceutical products are manufactured in accordance with area SOPs and current cGMP +… more
- Bayer (Berkeley, CA)
- …report and ensures resolution of critical equipment items * Develop, review and implement recommendations to improve reliability of infrastructure and production ... utility services; + Experience with regulatory and cGMP requirements for pharmaceutical manufacturing; + Knowledge and hands-on experience with pharmaceutical … more
- ICON Clinical Research (Blue Bell, PA)
- …medical input into study protocols and other trial-related documents. + Review clinical data , including inclusion/exclusion criteria and indication-specific ... medicine, we advance clinical research providing outsourced services to pharmaceutical , biotechnology, medical device and government and public health organizations.… more
- Sanofi Group (Cambridge, MA)
- …the agency of record in executing PSS patient tactics through promotional review approvals + Manage patient material inventory, utilization, print requirements, and ... or a related discipline + Minimum of 6 years of biotech and/or pharmaceutical industry marketing experience + Proven experience in pharmaceutical brand and/or… more