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Maintain active a New Jersey Alcohol and Drug Counselor certification, (CADC), or License, (LCADC) POSITION STATEMENT: The Alcohol and Drug Counselor main function is to provide substance abuse counseling services for assigned clients.
Full-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Spearhead the development and strategy of our client’s computational platform, integrating novel computational techniques and GPCR structural biology to aid drug discovery and development.
ExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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Our client is pioneering revolutionary patient treatments through a robust structure-based and computational drug discovery approach. The candidate should be driven by the latest innovations in drug discovery technology, possess strong leadership skills, and have a zeal for impactful change.
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The Alcohol and Drug Counselor main function is to provide substance abuse counseling services for assigned clients. Knowledge of addiction, substance abuse treatment services and counseling skills and theory.
Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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10+ years of experience in drug safety/pharmacovigilance within global clinical trial settings, with expertise in FDA, EU, ICH regulations, and Good Pharmacovigilance Practice guidelines.
ExpandApply NowActive JobUpdated 15 days ago - UpvoteDownvoteShare Job
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Knowledge of drug substance and drug product manufacturing processes as well as knowledge of other bulk characterization techniques (such as powder flow, rheology, friability, stickiness etc) is a plus.
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The Metropolitan Council's Occupational Health Department (A unit within Human Resources) has one (1) vacancy for a full-time DOT Drug and Alcohol Program Compliance Coordinator. The DOT Drug and Alcohol Program Compliance Coordinator.
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Extensive experience in late-phase drug product development and commercial development with CMC regulatory filings for the US (NDA), Europe (MAA), Japan, and China. Thorough understanding and working experience of pharmaceutical drug products concerning GMP, quality systems, ICH guidelines, FDA, EMA, and associated regulatory requirements.
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The qualified candidate must have at least 10 years (120 months) of Drug Safety/Pharmacovigilance and clinical development experience. Work together with other Drug Safety (DS) staff in managing the safety assessment of products, including review of individual and aggregate AEs and the scientific literature, preparing safety reports and communicating changes in the product risk profile to internal and external stakeholders.
Full-timeExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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Lead pre-formulation, final form selection, formulation and process development, clinical manufacturing, scale-up, tech transfer, process optimization, and process validation activities related to solid oral dosage and parenteral drug products.
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Under general direction and reporting to the Director of Wellness Services, the Alcohol and Drug (AOD) Prevention and Recovery Specialist provides individual substance use support for students.
Full-timeExpandApply NowActive JobUpdated 14 days ago - UpvoteDownvoteShare Job
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Abraxas Youth & Family Services is a national nonprofit human services provider dedicated to Building Better Futures for at-risk youth, adults, and families. Our diversified array of services includes alternative education, outpatient counseling, in-home services, shelter, detention, residential treatment and re-entry/transition services.
Full-timeExpandApply NowActive JobUpdated 12 days ago - UpvoteDownvoteShare Job
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Conduct modeling and simulation to inform drug discovery and translation of drug properties. Our aim is to find the right dose of the right drug for the right patient, embodying the model-informed drug discovery and development (MIDD) paradigm.
Full-timeExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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Playing a critical role as the drug product technical lead and CMC project lead, this position will be responsible for drug product development activities leading to NDA submission and commercialization and development and execution of the CMC strategy.
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The Manager will be responsible for oversight of safety operation activities with Arrowhead CRO vendors and partners, implementing Arrowhead safety reporting processes ensuring compliance with global requirements and monitor compliance of internal standard operating procedures related to drug safety & pharmacovigilance.
$120,000 - $155,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago
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