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Johnson & Johnson Innovative Medicine is recruiting for a Senior Scientist, Discovery Data Science to help advance Artificial Intelligence/Machine Learning (AI/ML) for Drug Discovery. The successful candidate will be actively involved in method development and project support in collaboration with data science teams, computational and experimental protein scientists, computational and medicinal chemists, project biologists, toxicology and pharmacokinetics and IT colleagues.
$113,000 - $195,500 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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The emphasis of the Drug and Alcohol Program is multi-faceted and includes meeting clinical benchmarks for quality care and productivity, ensuring proper care is being provided in accordance with service delivery contracts and providing ongoing staff development.
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You will work on the discovery and development of small molecules, biologics and non-traditional therapeutics like peptides, novel biological The Director is a skilled quantitative drug developer, with a strong, integrated understanding of the strategic elements of drug discovery and development.
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The Vice President of Pharmacovigilance (PV) will be responsible for the global, strategic, and operational oversight of the quality and compliance of pharmacovigilance, drug safety, and clinical risk management activities in support of Larimar worldwide and in fulfillment of global legislation and regulations.
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Understanding of the drug development process, including regulatory requirements related to pharmacokinetics and pharmacodynamics. The ideal candidate will have extensive experience in the application of pharmacokinetic (PK) and pharmacodynamic (PD) principles to drug development, with a focus on modeling and simulation to predict drug behavior, optimize dosing, and improve therapeutic outcomes.
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The role collaborates closely with Drug Safety Operations staff (on medical aspects of ICSRs) and Clinical Development (medical ICSR discussion and follow-up, as well as safety surveillance.
$226,000 - $321,500 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Knowledge of the drug development process and clinical research methodologies including experience in clinical trial design, data analysis/statistics and data interpretation; knowledge of regulations, ICH/GCP, adverse event management.
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Eurest services maintains a drug-free workplace. Job SummaryThe Solutions Development Manager will participate and play a critical role in the following activities: Participates in bid evaluation.
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This individual will identify and implement tested industry methodologies associated with the appropriate use of mathematics and statistics, They will work with their pers to identify and deploy statistical, mathematical, and graphical approaches for innovation, development, validation, and base business support of drug product manufacturing and packaging processes.
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This opportunity offers the following: Competitive Compensation & Generous Paid Time Off Excellent Medical, Dental, Vision and Prescription Drug Plans (K) with company match and discounted stock plan SoFi Student Loan Refinancing Program Career development opportunities within UHS and its + Subsidiaries.
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Equivalent combination of education and experience Experience/The Ideal for Successful Entry into Job: Drug development experience in biotechnology or pharmaceutical industry, or a combination of academia and industry.
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Devise model informed drug development strategy via application of quantitative methods to integrate knowledge of PK, PD (e.g., biomarker, efficacy, and/or safety), patient characteristics, disease states, competitive and landscape to influence go/no go decisions, support patient sub-population, dose and dosage regimen selection, and optimize study designs throughout drug development.
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The activities include review of clinical study protocols, design of clinical labels, preparation of packaging and labeling requests, management of depot and site shipments, monitoring study drug inventory levels, and assist in supply planning and forecasting.
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Knowledge of GMP batch record development, review, and approval processes. Perform drug accountability with depots/clinical sites and Sponsor inventories. The selected candidate will independently coordinate clinical supply activities for clinical studies in support of development programs.
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Drug screening, #THC motor vehicle record check and criminal background check will be performed on all new hires. We are looking for leaders who are looking for a company with a strong focus on employee development and career advancement.
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drug development jobs in Conshohocken, PA
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