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Basic knowledge of medical terminology and a working knowledge of drug development services desired; We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries.
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Sound knowledge of drug development and understanding of FDA and ICH GCP guidelines. Working knowledge of relevant therapeutic areas and experience working within development of preclinical through translational stage clinical studies.
RemoteExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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10-15 years of experience in pharmaceutical/biotech industry, including drug substance/drug product manufacture, development, and/or quality. 10-15 years of experience in pharmaceutical/biotech industry, including drug substance/drug product manufacture, development, and/or quality.
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Experience in Sales, Business Development or Key Accounts management. Sell Temperature Control Storage to CDMO/Pharma who manufacture API's & Drug substance. Supervise Sales, Business Development, and Marketing efforts.
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They have gone through sustained growth over the last few years, with an expansion strategy combining both site acquisition and continued investment & development of existing facilities. Our client is an industry leading CDMO who offer end to end services from discovery to commercialisation, with varying capabilities across small & large molecule development & manufacture.
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A leading provider of drug, alcohol, addiction, trauma, depression, anxiety therapies is looking for a Business Development Rep. You will have the opportunity to personally interact with physicians, hospital administrators, social workers, case managers and other clinical personnel to strengthen business relationships and gain referrals.
$150,000ExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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In addition, the Pharmacy Business Integration Specialist is responsible in supporting the Business Management space to achieve successful development of the Pharmacy Benefit Management Solution in support of the Medicaid program.
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Good knowledge of statistics and drug development processExperience as a lead programmer for NDAs/BLAsExperience overseeing the work of internal contractors and external vendors (CROs)Experience in pharmacokinetics/pharmacodynamics modeling a plusFamiliarity with CDISC standards, including SDTM and ADaM modelsSolid verbal and written communication skills.
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As a digital project manager, you will join a team of professionals working in web design, web development, user experience and information architecture, and search engine optimization. The unlawful or unauthorized use, abuse, solicitation, theft, possession, transfer, purchase, sale, or distribution of controlled substances (including medical marijuana), drug paraphernalia, or alcohol by an individual anywhere on Reingold premises, while on company business (whether or not on Reingold premises), or while representing the company is strictly prohibited.
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Familiarity with clinical trials terminology, FDA, PMDA, and ICH guidelines as well as the drug development process. Experience with any data analysis package such as SPSS, SAS, R, or MATLAB.
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Ability to develop software solutions in conjunction with data scientist, statistician, and study team to anticipate and meet client needs. YPrime's Customer Experience and Data Science team is looking for an Associate Data Scientist to be responsible for supporting the teams activities for the collection, cleaning and transformation of data to meet our customer and company needs.
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Accountable for clinical parts of regulatory documentation (e.g. meeting packages, investigational device exemption [IDE], investigational new drug [IND] applications, and sections of marketing applications [PMA/NDA/MAA/CTD] or other submissions depending on host country.
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To join a well-established, global clinical research organization focused on improving the drug development process and access to therapeutics. SAS, Programmer, statistics, CDISC, SDTM, ADaM, CRO, clinical research, pharmaceutical, biotechnology, clinical data, data management, EDC, Electronic Data Capture, Medidata, Rave, Oracle, Inform, datasets, TLF, tables, listings, figures, programming, benefits, medical, dental, vision, 401k, Remote.
Full-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Knowledge of the drug development process and FDA and ICH Guidelines required. In this position, you will provide overall technical, administrative and functional oversight for the Biostatistics functions of the organization which include statistical consulting, statistical analysis plans, protocols, study reports, and other statistical sections of NDAs and other drug, device, or biologic regulatory submissions.
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Provide expertise and business support to the Pharmacy and Ancillary Services Business Unit in the development and implementation of the Medicaid Enterprise Modular Pharmacy Business Management (PBM) Solution.
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drug development jobs in Raleigh, NC
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