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Accountable for the scientific guidance and design of the bioanalytical translational and clinical strategies and the execution (e.g. Biomarker) of therapeutic programs with different modalities.
$140,000 - $200,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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This role will develop and lead all medical affairs activities ensuring partnership within the team (medical strategy, scientific communications and publications) all key Medical Affairs functions (Medical Excellence, HEOR, Field Medical, Medical Information) as well as maintaining a high-level cross-functional collaboration across the organization to ensure alignment and One Insmed approach.
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The Director of Clinical Pharmacology role within Clinical Development organization will provide leadership and expertise to support assigned clinical pharmacology projects in the clinical development programs for an expanding portfolio of small, biological and inhaled molecules across several disease areas.
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Works closely with the Regulatory Affairs labeling group regarding package insert changes to assess and determine the impact of proposed labeling changes on product promotion. Strong business acumen and the ability to see business drivers outside of regulatory affairs.
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Creates demand for BMS medicines by articulating in a balanced manner the clinical and scientific rationale for use of products in appropriate patients. - Excellent communication and presentation skills to articulate scientific and clinical data in an easy-to-understand manner to help HCPs best serve their patients.
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NJ candidates: hybrid schedule (2x week) Boston candidates: in-person training, fully remote after •Education: minimum qualification is a Bachelors in Biology, or Pharmacy •Must-Have Experience with: VEEVA, life-cycle tools, MS Suite especially Word & Excel •Preferred experience: Regulatory affairs •Work Experience: 5 years of industry experience.
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Plan and execute publication and clinical communication strategy in coordination with Scientific Communications. As Medical Director at Genmab, you will be accountable for the medical oversight of one or more clinical trials, medical review and communication of data, and medical input into regulatory documents, and presentations.
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Ability to communicate scientific or clinical data accurately and convincingly to help physicians best serve their patients. - Advanced scientific degree and/or preferred 5+ years of pharmaceutical or biotechnology experience as healthcare sales / MSL / HCP / nurse.
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Provides scientific and technical expertise by collaborating closely with Translational Science Leads, Clinical Biomarker Leads, Biosample Operations, Clinical Leads and Regulatory Liasions to ensure sucessful implementation of CDx and data collection.
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QuidelOrtho unites the strengths of Quidel Corporation and Ortho Clinical Diagnostics, creating a world-leading in vitro diagnostics company with award-winning expertise in immunoassay and molecular testing, clinical chemistry and transfusion medicine.
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Foster collaboration, alignment and seamless working across R&D and GCSO functions, including the Clinical Development Team (CDT), Commercial, Medical Affairs, and Global Market Access COE to ensure optimal launch readiness for the brand.
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Licensed Clinical Social Worker (LCSW)/ Licensed Marriage and Family Therapist (LMFT) / Licensed Professional Counselor (LPC). We are actively looking to hire talented Licensed Therapists in the Princeton Junction, Brick, Eatontown, Piscataway, North Brunswick, Mt Laurel, Lyndhurst and Cherry Hill, NJ area who are passionate about patient care and committed to clinical excellence.
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As a Senior Manager, Global Procurement you will be accountable for supporting the definition and implementation of the global Clinical Core (IRT, eCOA) and Digital Health Technology Category strategy.
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The HORIBA Group of worldwide companies provides an extensive array of instruments and systems for applications ranging from automotive R&D, process and environmental monitoring, in-vitro medical diagnostics, semiconductor manufacturing, and metrology, to a broad range of scientific R&D and QC measurements.
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This individual will support the organization in its build and ramp-up of clinical production and facility approval of a state of the art cell therapy facility. This position will be responsible for maintenance support and mechanical system operations for cGMP Clinical and Commercial Cell Therapy Manufacturing facility.
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clinical scientific affairs jobs Title: director Company: Regeneron Pharmaceuticals Inc in Bridgewater, NJ
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