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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.
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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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Piper Companies is looking for an experienced Senior Statistical Programmer (PK/PD) to join a well-established, global clinical research organization focused on improving the drug development process and access to therapeutics.
Full-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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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.
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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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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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Responsibilities:Create or review and approve CDISC-compliant datasets and corresponding documentation for electronic submission to regulatory agencies. Bachelor's degree in computer science, Statistics, Mathematics, Life Sciences or other relevant scientific fields; master's degree preferredMinimum of 3 years of experience in developing software for clinical trials using the SAS systemSkilled in programming with SAS. Knowledge of additional programming languages a plus.
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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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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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In-depth knowledge of the pharmaceutical and biotech industries, clinical trials, and drug development and commercialization (strongly preferred) Science 37 is accelerating the research and development of breakthrough biomedical treatments by bringing clinical trials to patients' homes.
Full-timeExpandApply NowActive JobUpdated 12 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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Basic understanding of CROs and scientific & clinical data/terminology, & the drug development process preferred. Strong industry experience, technology-enabled services, and a data-driven approach to drug development make MMS a valuable CRO partner, creating compelling submissions that meet rigorous regulatory standards.
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With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners’ most high-profile drug and device programs.
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The experience of the Verona team, and its highly effective leadership allows us to challenge the status quo in drug development and commercialization. We do this principally through the development of our first-in-class molecule, ensifentrine.
ExpandApply NowActive JobUpdated 16 days ago - UpvoteDownvoteShare Job
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Demonstrated understanding of the overall drug development process with clinical trial design, study implementation, sponsor/site interactions, scientific and clinical methodology, protocol design, project management and regulatory requirements for clinical studies to be reviewed by health authorities.
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drug development jobs in Raleigh, NC
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