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As a Graduate Rotation Analyst, you will perform the same tasks as our entry level Analysts and have an opportunity to learn the methods, tasks, and objectives each of these groups complete in their day-to-day support of NRG’s operations and business strategy.
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Possess understanding of drug development experience and understand what it takes to shepherd a molecule through its lifecycle. Must demonstrate knowledge of the overall drug development process relevant to biotech/ pharmaceutical companies; commercial launch experience and familiarity with drug development experience is highly desirable.
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In this role, the Manager will play a critical role in the development of the talent within the team and contribute to broader Talent Acquisition strategy and execution. CoStar Group is an Equal Employment Opportunity Employer; we maintain a drug-free workplace and perform pre-employment substance abuse testing CoStar Group (NASDAQ: CSGP) is a leading global provider of commercial and residential real estate information, analytics, and online marketplaces.
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Managing the performance and development of 6 salary logistics coordinators and 3 hourly oil-shed operators. Unilever at a Glance | Working at Unilever | Powering our Purpose | Planet & Society | Unilever’s Brands | Unilever on LinkedIn | Strategy | Unilever | Diversity, Equity & Inclusion | Careers at Unilever | Benefits, Learning, & Wellbeing | Latest News About Unilever.
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The Executive Director, CMC Regulatory Affairs is responsible for developing and directing the regulatory CMC strategy, objectives, and programs pertaining to development and marketing of drug products.
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Accordingly, the Clinical Biomarkers & Diagnostics (CBD) function plays a critical role in advancing our drug development programs and is accountable for the development of biomarker and diagnostics strategy across our pipeline.
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Within the industry landscape, increasing demand for observational research (now commonly referred to as real-world evidence [RWE]) from regulatory and reimbursement authorities makes observational research a key component of drug development and commercialization.
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Working with an experienced Program Manager and a cross-functional team, the PTL shapes the Program strategy, goals, priorities, and plans, bringing both a ‘future-orientation’ toward the ultimate goal of broad, global commercial access for patients in need, and a “pragmatic-orientation” to chart the path, mitigate risks, cultivate options, and lead through complex drug development decisions.
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The success of our lead product has provided a solid commercial foundation allowing us to reinvigorate our research efforts, and grow our team in areas such as Drug Discovery, Clinical Development and Commercial.
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This Senior Manager position and their direct reports will be collaborating with the following groups: small molecule drug substance (development and manufacturing), drug product (development and manufacturing), analytical, regulatory, quality (QA and QC), supply chain, packaging/device and labeling, and the Global Development and Program Strategy teams.
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Engage and negotiate with partnering groups within and outside Research, such as Clinical Pharmacology and Precision Medicine, Pharmaceutical Sciences, Early and Late Clinical Development, Legal/IP, Regulatory Strategy, and Project & Portfolio Management to ensure critical path activities are identified and prioritized to achieve Research project objectives and milestones.
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Knowledge of the drug development process, Good Clinical Practices (GCP) and Good Pharmacovigilance (GVP), including worldwide PV regulations and their application to safety science activities (aggregate PV reports, risk management plans, signal detection, clinical trials and clinical development.
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The Regional Sales Manager works collaboratively with the Sales Executive, Sales Support, Solution Consultant and Sales Leadership teams worldwide to develop the sales strategy for maximizing sales across the customer base.
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You possess extensive experience in leading cross-functional teams to drive all Chemistry, Manufacturing, and Controls aspects of oligonucleotide drug development and commercialization. As the CMC Lead for antisense oligonucleotides (ASOs), you are a highly skilled and motivated professional with a deep understanding of oligonucleotide (or related compound) development and manufacturing processes.
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The team strives to deliver compelling preclinical, clinical and translational data packages providing confidence in the dosing strategy, tolerability profile and therapeutic efficacy of our candidate drugs to support investment in late stage clinical development, leading to drug approval.
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