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And minimum 7 years global Drug Safety/Pharmacovigilance clinical trial and post marketing experience in a pharmaceutical or biotechnology industry in positions of increasing technical and leadership responsibility.
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Dive into the dynamic world of AI and Digital Technologies at Genmab The Role: As an Associate Digital Product Manager in IT & Digital, you will have a critical role in overseeing the product strategy, development/implementation and management of technology products in different focus areas in Global Drug Safety and Pharmacovigilance.
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Understands, conducts, and documents appropriately Dialysis/Apheresis machine safety tests/alarm tests, equipment calibration, dialysate testing, machine safety tests, functional testing, and internal and external disinfection on all water & dialysis machines, and complies with the documentation/notification standards per FMS policies.
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This is a non-laboratory, management position, requiring excellent interpersonal and writing skills, a high level of organization, diplomacy, focus, ability to work under tight deadlines, and strong affinity with biomedical research and knowledge of how Translational Research, Precision Medicine, Pharmacology, and Toxicology impacts drug development.
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Targeting 10 years of experience as lead statistician on clinical trials in the pharmaceutical industry with significant experience in rare disease drug development. Maintain thorough understanding of current regulatory guidelines and requirements relevant to rare disease drug development.
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The successful candidate will be a valuable member of a growing energetic team of cell scientists, whose responsibilities include stable cell line production, generation of cell biomass and assay ready cells, supporting drug development efforts at different levels and recombinant protein expression in mammalian cells.
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As the business support manager for several critical Public Safety systems, this role is responsible for business technology management, oversight of service analytics, and multiple functional system requirements (training, user acceptance testing, business stakeholder management, etc.
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Working with SPC, SAP, Food Safety and Quality Plans, Water Treatment, Batching Process, Internal Sanitation, Microbiology, Environmental Monitoring Programs, and Product Testing Requirements. Long term goal is to promote to a SQF practitioner and Quality Manager.
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Performs duties as assigned by Pharmacy Manager, Staff Pharmacist and Store Manager including utilizing pharmacy systems to enter patient and drug information, ensuring information is entered correctly, filling prescriptions by retrieving, counting and pouring pharmaceutical drugs, verifying medicine is correct, and checking for possible interactions.
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Qualifications & Experience:MD, PhD, DVM, PharmD, MBA or equivalent advanced degree of relevance, in the drug development process. Key ResponsibilitiesStrategy and Execution:Uses an understanding of disease biology, the drug development process (particularly cross-functional connectivity), and relevant late-stage challenges (e.g., trends in disease area therapeutic advances, and evolving regulatory, patient advocacy and market access environments) to create a vision for each asset, then design and execute effective development programs in support of the overall R&D portfolio goals.
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Pre-employment background screening (criminal and MVR ) a nd drug testing (including for marijuana) are required for all positions. We work with an exciting variety of nationwide supermarkets (ShopRite, Trader Joe's, Whole Foods, etc.
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PhD/MD/PharmD or commensurate with experience including thorough understanding of drug development and scientific principles and at least 7 years of organizational leadership. Proven track record in the delivery of successful major filings (NDA / MAA / J-NDA / China NDA), preferably in different therapeutic areas strong depth and breadth of knowledge of the submission process and significant experience in writing highlevel summary documents for global registrations; experience in process development and preparation of key regulatory documentation such as protocol development, clinical study report, Investigator Brochure, and safety aggregate reporting.
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The Sr. Application Architect collaborates with OmniChannel Customer Experience team to provide technical solutions that include designing omni channel experiences including Web, Email and SMS touchpoints and help with development, testing and rollout of the solutions using Agile methodology.
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Proficiency in Python/R and SQL, or similar technologies, for hands-on data wrangling, and exploratory data analysis and hypothesis testing. We do not discriminate on the basis of age, ancestry, color, gender identity or expression, genetic predisposition or carrier status, marital status, national or ethnic origin, race, religion or belief, sex, sexual orientation, sexual and other reproductive health decisions, parental or caring status, physical or mental disability, pregnancy or maternity/parental leave, protected veteran status, status as a victim of domestic violence, or any other classification protected by applicable law.
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A Senior Data Management Professional (DMP) is a key role within our organization responsible for optimizing our data for clients and improving our data operations. g Qlik, Tableau, Power BI. This role encompasses various specialty areas, including Data Engineering, Data Product Ownership, Data Modeling & Data Quality and requires a solid background in data management.
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drug testing jobs Title: sales manager Company: Nrg in Cranbury, NJ
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