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Health Safety Environment Sr Manager, P&BPrinceton, NJOnsiteAs the Health Safety and Environment Sr Manager, you are responsible to provide HSE leadership, knowledge and guidance across all operational departments and teams of the site.
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At Genmab, we’re committed to building extra[not]ordinary futures together, by developing antibody products and pioneering, knock-your-socks-off therapies that change the lives of patients and the future of cancer treatment and serious diseases.
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The evidence-based history of Applied Behavior Analysis (ABA) therapy has proven it to be a best practice model used to support and provide effective treatment to individuals with Autism Spectrum Disorder (ASD) as well as other behavioral and developmental disabilities.
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Manager – Digital, Biopharma Dev & Chemistry, Manufacturing, and Controls (CMC)ZS is looking for an experienced team member that brings pharmaceutical drug development and tech transfer knowledge with a focus on digital transformation in this space.
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And through a broad range of genomics research, and by collaboration with cross-functional teams, this position offers an exciting opportunity to enable immunology discovery groups to launch novel programs, validate drug targets, profile pharmaceutical candidates, and assess preclinical biomarkers.
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Treatment caseload includes motor vehicle accident and work accident cases with a focus on trauma and mild TBI. Our Director of Training, Jonathan H. Mack, Psy. D., ABN, FACPN, is a board-certified neuropsychologist with over 30 years of experience in forensic neuropsychology and forensic psychology, having testified over 200 times in a wide range of jurisdictions and states.
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Performs duties as assigned by Pharmacy Manager, Staff Pharmacist and Store Manager including utilizing pharmacy systems to enter patient and drug information, ensuring information is entered correctly, filling prescriptions by retrieving, counting and pouring pharmaceutical drugs, verifying medicine is correct, and checking for possible interactions.
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Responsibilities The Patrol Lieutenant, reporting to the Patrol Captain, is an administrator of the Department of Public Safety (DPS). Five-year tenure in the Princeton University Department of Public Safety or comparable experience as a Campus Law Enforcement Officer.
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Chemistry is a core capability in Small Molecule & Drug Discovery with innovative scientists working in medicinal chemistry, radiochemistry, analytical chemistry, and large-scale synthesis. Bristol Myers Squibb encompasses a broad range of disciplines to enable a robust pipeline of drug candidates aimed at serious diseases.
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Knowledge and understanding of drug development including regulatory requirements and quality standards applicable to nonclinical and clinical laboratories (e.g., GLP, GCP, ISO). For more than 20 years, its passionate, innovative and collaborative team has invented next-generation antibody technology platforms and leveraged translational research and data sciences, which has resulted in a proprietary pipeline including bispecific T-cell engagers, next-generation immune checkpoint modulators, effector function enhanced antibodies and antibody-drug conjugates.
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Provide strategic CMC regulatory expertise for development project teamsProvide strategic input to development & GO teams to mitigate drug supply issues. The team also supports Medical Information to build/maintain database to address external questions regarding drug products.
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ComAbout LifeStance Health LifeStance is a national provider of mental healthcare services focused on evidenced-based, medically driven treatment services for children, adolescents and adults suffering from a variety of mental health issues in an outpatient care setting, both in-person at its clinics nationwide and through its digital health telemedicine offering.
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Safe and timely execution of Phase I studies; close collaboration with internal and external clinical study support staff and scientists (including discovery research, biostatistics, drug metabolism, modeling and simulation, regulatory affairs, and global clinical trials operations.
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Significant experience in pharmaceutical/biotechnology and extensive knowledge of drug development processes, ICH-GCP guidelines, 21 CRF Part 11, and major Health Authority regulations as they pertain to the operational aspects of clinical trials.
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High level of computer expertise in multiple industry-wide software products, such as:MS Office ProductsScheduling software such as Primavera and MS ProjectClient ERP systems such as JDE, QUAD, SAP, ARIBA, CONCURPPM Software: Prolog, Proliance, Prism G2, Procore, Cleopatra, Cora SystemsContext, Environment, & SafetyA safety-minded individual who must comply with the IPS Mission Zero Safety policy.
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treatment drug safety jobs Company: Genmab A S in Princeton, NJ
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