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RequirementsA PhD in oncology/immuno-oncology, or related field, with at least eight or more years of translational research, applicable biomarker, and/or clinical trial experience.
$237,500 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Bristol-Myers Squibb is actively conducting translational medicine research to further our understanding of cancer biology and to identify which patient populations may be more likely to derive benefit from Immuno-Oncology (I-O.
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Specific experience in the diagnostic industry, oncology biomarkers, diagnostic business development, and/or certification in laboratory medicine (e.g. ASCP) is a plus. The Associate Director of Diagnostic Sciences provides subject matter expertise related to development and execution of the companion biomarker diagnostic programs for BMS product development and brand teams.
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1 Year residency and/or Board-Certified Oncology Pharmacist (BCOP) preferred At least 7 years of pharmacy experience preferred. 1 Year residency and/or Board-Certified Oncology Pharmacist (BCOP) preferred At least 7 years of pharmacy experience preferred.
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Disseminate MSK oncology nursing practice standards and outcomes through abstract submission, podium presentation, and evidence-based research findings. A successful collaborator with the ability to engage others with different points of view and priorities You will: Provide clinical leadership in the areas of evidence-based oncology nursing practice, education, consultation, and research.
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But working at Bristol Myers Squibb is anything but usual.
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Today, we're advancing programs in Endocrinology Rare Disease and Oncology. Bachelor’s degree in marketing, business, or related field 8+ years’ experience in pharmaceutical marketing, preferably with brand management experience Proficiency in core principles of brand management, including brand positioning, value proposition, segmentation, messaging, and investment optimization.
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Eugia is a US-based independent specialty pharmaceutical company focused on generic sterile injectables, oncology, hormones, and ophthalmic medicines. Prior generic pharmaceutical marketing experience required.
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Identify develop operational institutional pathways to grow scientific engagements research and data for the enterprise with a special focus on community oncology centers and accounts for ongoing working groups and consortium support Contributes to the scientific affairs HCE partnership execution with select external research partners to maximize effective and compliant delivery of research with external organizations.
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Specialty Pharmacy Technician Requirements:High School Graduate/GED/ Equivalent WorkCompletion of a Pharmacy Technician ProgramNew Jersey Board of Pharmacy Technician registrationCertified Pharmacy Technician (CPhT) from the Pharmacy Technician Certification Board (PTCB)Minimum 2 years of previous pharmacy technician experience, specialty pharmacy (oncology) experience preferred.
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Kyowa Kirin is a fast-growing global specialty pharmaceutical company that applies state-of-the-art biotechnologies to discover and deliver novel medicines in four disease areas: bone and mineral; intractable hematologic; hematology oncology; and rare disease.
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Responsibilities Collaborate with extended Business Development and specialty therapy area teams to refine Sun’s strategy for growth in current areas of ophthalmology, dermatology, and onco-derm; and evaluate opportunities to expand into additional therapy areas such as oncology and rheumatology.
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Collaborate with extended Business Development and specialty therapy area teams to refine Sun’s strategy for growth in current areas of ophthalmology, dermatology, and onco-derm; and evaluate opportunities to expand into additional therapy areas such as oncology and rheumatology.
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Focusing on Oncology, this business critical position is heavily focused on Risk Management / Safety Surveillance and will oversee the Safety / Risk profiles for all assigned compounds within the organization.
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Under the leadership of Regulatory Affairs, the incumbent manages global regulatory operational activities (except Asia) for all Taiho Oncology, Inc. (TOI) projects, provides strategic regulatory operational guidance during drug development, approval, post-approval, and commercialization, in coordination with internal staff and external consultants/contractors.
$210,000 a yearFull-timeExpandApply NowActive JobUpdated Today
immuno oncology jobs in Princeton, NJ
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