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PhD, Pharm D, MS or equivalent degree preferably within the medical, biological, pharmaceutical science or related discipline. To help develop and deliver novel antibody therapies to patients, Genmab has formed 20+ strategic partnerships with biotechnology and pharmaceutical companies.
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Resource Label Group, LLC is a leading full-service provider of label and packaging solutions with a diverse product offering which includes pressure sensitive labels, shrink sleeves, RFID/NFC technology, sustainable product solutions, scent activation technology, pharmaceutical packaging and fulfillment services.
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Minimum of 7-10 years of experience in pharmaceutical market access marketing, pricing, and/or brand marketing, with a focus on payor and channel marketing. Strong understanding of pharmaceutical coverage in the government and commercial channels; pricing dynamics; reimbursement models; and contracting strategies across various payer segments (e.g., commercial, Medicare, Medicaid, VA/DHA) and coverage pull-through messaging and materials.
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The Scientific Team at Russell Tobin & Associates is supporting an exciting pharmaceutical organization that has an opening for a Clinical Quality & Compliance Specialist near Princeton, NJ! 6+ years R&D focused pharmaceutical experience in a GCP regulated environment.
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D. or Master degree in Bioanalytical, pharmaceutical, immunology, biological sciences, or a related field. The incumbent will provide leadership for the performance of the Small Molecule, Large Molecule and Central Lab functions at the WuXi NJ site, lead the team in bioanalytical sciences, GLP operations, and business aspects, and to collaborate with WuXis Bioanalytical and Central Labs in China to promote synergy in supporting global clinical and non-clinical studies.
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Maintains understanding of laws and regulations, enforcement actions and evolving practices relevant to pharmaceutical ethics & compliance and proposes updates to Ethics & Compliance program, as appropriate.
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Broad knowledge of secondary pharmaceutical data sources such as Retail & Non-Retail data, Medical & Pharmacy Claims, EMR, Lab Test/Diagnostics, Chart Audits, Patient Hub & Specialty Pharmacy Data, 852/867 EDI and Health System/Payer – Plan hierarchies.
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At Genmab, we’re committed to building extra[not]ordinary futures together, by developing antibody products and pioneering, knock-your-socks-off therapies that change the lives of patients and the future of cancer treatment and serious diseases.
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Successful candidate will have a strong understanding of the drug development process from preclinical pharmacology through to regulatory approval and the principles, concepts, practices, and standards of pharmaceutical program management.
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Minimum work experience: Minimum 15 years of US pharmaceutical or biologics sales management experience including a minimum of 5 years as a Regional Business Director. Advanced understanding of market access dynamics in the pharmaceutical industry to include payers, specialty pharmacies, pharmacy benefit managers, Integrated Delivery Networks (IDNs), etc.
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Must have Master’s in Chem, Pharmacology, or rel sci field and 3 yrs laboratory exp in pharmaceutical industry with cGMP requirements. Alternatively, must have Bach’s in Chem, Pharmacology, or rel sci field and 5 yrs laboratory exp in pharmaceutical industry with cGMP requirements.
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5+ years working within the pharmaceutical industry inclusive of experience tailoring media activations within HCP and DTC campaigns. The Media Director will ensure both our internal and external partners are maximizing their relationships through media strategy and lead the day-to-day operations of the media agencies.
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Support start-up of biotechnology, cell & gene therapy, and pharmaceutical manufacturing facilities. 7-15 years of experience in the biotech/biologics, cell/gene therapy, and/or pharmaceutical/drug sectors.
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Founded in 2002, Clinical Resource Network (CRN), a division of Solomon Page, provides clinical research and talent solutions for pharmaceutical, biotech, and medical device companies. Pharmaceutical industry experience in Clinical Development (+ 6 years’ experience) for neuroscience products would also be considered.
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Advanced understanding of pharmaceutical development and CMC regulatory affairs including regulatory guidelines, federal regulations and legal considerations. Minimum of 10 years of pharmaceutical industry experience, at 8+ years in Regulatory Affairs with emphasis on CMC. Must have managerial experience.
$80,000 - $170,000 a yearFull-timeExpandApply NowActive JobUpdated 4 days ago
pharmaceutical entry jobs in East Windsor, NJ
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