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EAC Network, a not-for-profit social service agency that empowers, assists, and cares for over 62,888 people in need through 100 programs across Long Island and NYC, seeks a Case Manager Community Transitional Case Management (CTCM) to work full time for its Brooklyn Community Re-Entry Assistance Network (CRAN) program.
$28.93 an hourFull-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Extensive experience in vulnerability management, patch management, and configuration management best practices. to join our team at the Drug Enforcement Administration. Maintain patch and vulnerability management practices to protect against exploitation.
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Utilize relevant market intelligence resources to offer insights into pursuing traditional and AI-driven drug development partnership opportunities. 10+ yrs of business development experience within the pharmaceutical industry with a preference for oncology drug development expertise.
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Collaborate with cross-functional stakeholders including DMPK, translational medicine, clinical development, clinical operations, regulatory, CMC, and project management to ensure completion of clinical pharmacology deliverables.
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Adherence to patient management programs through call cadence schedules, medication management programing, drug counseling and provider collaboration. Counsel and educate new/existing oncology patients on specialty drug therapies via phone.
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Saab is a federal government contractor and adheres to policies and programs necessary for sustaining drug-free workplaces. Manage data using PDM and follow processes related to configuration management.
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Depending on your eligibility, options for part-time employees include: medical/prescription drug coverage (with a Health Savings Account feature), dental and vision options; employee life insurance; 401(k) with PNC match, pension and stock purchase plans; back-up child/elder care; adoption, surrogacy, and doula reimbursement; educational assistance, including select programs fully paid; a robust wellness program with financial incentives.
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Driving accountability and goal alignment; revenue retention and growth strategies including value realization, renewal execution, risk management, and customer growth. Experience: 5+ years customer success or account management experience.
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Advising and supporting a global team of 5-6 Business Development Managers as well as the CHC Product Management Team responsible for CHC business categories, including Dermal Drug Delivery, Eye Care, Cough & Cold, Allergic Rhinitis, and VMS.
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Demonstrated experience in inventory management (specifically IXRS systems) and forecasting global drug supply requirements. Proven experience in clinical supplies environment with a strong understanding of clinical study design, execution, and impact of study drug supply from study start-up through trial completion.
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Clinical trial, drug development, Oncology, Phase I-III, FDA, ICH Guidelines, GCP, vendor management, APAC regulations, travel. This role is a unique opportunity for an experienced Clinical Operations Professional with technical expertise in managing Phase I-III clinical trials in an industry setting and a strong knowledge of clinical operations, Good Clinical Practice (GCP), and US Food and Drug Administration (FDA) regulatory requirements.
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Oversee the drug substance, drug product, packaging/labeling/serialization, third-party logistics vendors for production activities of early and late-phase therapeutic areas. Building upon this track record of establishing a robust pipeline through in-licensing and acquisition of novel assets and technology platforms, Roivant is currently building new capabilities in drug discovery and expanding upon existing development disciplines to become the leading tech-enabled pharmaceutical company.
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12+ years of experience as a biostatistician working in clinical trials, with a deep understanding of statistical methods in drug development. This candidate will have the opportunity to be responsible for the management, oversight, and direction of multiple projects, author SAPs (including TLF shells), develop cross-functional data review plans, and help to represent the company to regulatory authorities.
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The American drug supply is highly reliant on this plant for pain and addiction treatment. site Accounting (Cost Accountant, General Accountant, Payroll & AP) and Management Information Services activities and personnel to enhance site productivity and results.
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Performs other operational readiness tasks as required, such as: document review/approval, team onboarding, and materials management. Please note: Supervisor/Manager level candidates who have upstream manufacturing experience and API/drug substance, are highly preferred.
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management drug jobs in Queens, NY
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