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BS in Sciences from an accredited institution (can also include Social Sciences) 1-3 years of experience in a technical fragrance development/evaluation/sensory role either with a supplier or a consumer package goods company.
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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 role requires 5+ years of Software Development experience , in-depth knowledge of Python, Django, JavaScript (React/Redux preferred) , and hands-on experience with AWS. Jack-of-all trades; Expert in one - Someone who can do anything from optimizing SQL query to writing maintainable CSS and everything in between, but they still have a preferred part of the stack and are comfortable with full-stack.
Full-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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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.
ExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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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. Regularly interfaces with team members in R&D including Biostatistics and SAS Programming staff, Data Management, clinical research and operations teams, regulatory affairs, clinical pharmacology, medical writing, medical affairs and quality management.
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Use experience with: SAS and programming languages for derived analysis datasets and TFLs; XML, Pinnacle 21; handling and processing of upstream data (multiple data forms, workflow, eDC, SDTM); providing outputs to meet downstream requirements (ADaM, Data Definition Table, e-submission); and CDISC standards and relational database to p rovide comprehensive programming expertise to clinical project teams to support the development, regulatory approval and market acceptance of BMS products.
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Advanced Tableau, Spotfire, Power BI, SAP Business Objects (BO) skills with + years of development experience. Ability to lead the development of critical path analyses and support scenario planning.
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There is strong preference for subject matter expertise related to immunohistochemistry and pathology assay development. SummaryThe Director of Solid Tumor Oncology Diagnostic Sciences is responsible for providing enterprise capabilities for the development and delivery of diagnostic products that support Precision Medicine therapeutic assets.
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The Director, Drug Safety is responsible for planning, directing, coordinating and prioritizing activities of the product safety team and providing oversight of Pharmacovigilance (PV) vendors in all aspects of PV activities for products both marketed and in development.
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DescriptionJanssen Research & Development, LLC is recruiting for an Associate Director, Clinical Pharmacology and Pharmacometrics (CPP) to be located in Spring House, PA, Titusville, NJ or Raritan, NJ.At the Janssen Pharmaceutical Companies of Johnson & Johnson, we are working to create a world without disease.
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As a member of UDC’s Chemical Business, this position will work closely with UDC’s HQ team, UDC’s contract manufacturing partner (PPG), and other UDC subsidiaries in the development and manufacture of UDC’s OLED materials in a fast-paced, non-GMP environment.
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Our team is excited to welcome a dynamic Business Development Manager who can bring their expertise to the table. Relevant government and/or industry experience with an established network across government, and militaryWhat We Offer:Whether you’re just starting out on your career journey or are an experienced professional, we offer a total rewards package that goes above and beyond with compensation; healthcare, wellness, retirement and work/life benefits; career development and recognition programs.
$130,000 - $272,000Full-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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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.
ExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Prior clinical research or related experience (e.g. monitoring of clinical studies, knowledge of drug development phases, statistical research methodology experience) From health-care-provider interactions and developing and implementing regulatory strategies with the FDA to providing medical education and collecting data to support efficacy and new product development, CMR is involved.
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401(k) with company match Wayfair company discount Growth opportunities (Career development and upskilling: Learn to use equipment such as: Forklift, Cherry pickers, reach trucks, clamps and so much more.
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