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Serve on cross functional drug product (DP) working group and supports LVV lyophilized DP activities through filing and Process Performance Qualification (PPQ), site characterization plan and execution, tech transfer control strategy, process development, PPQ readiness, PAI (Pre.
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Trusted by leading health systems, payers, biopharma companies and patients alike, Biofourmis' connected platform improves patient outcomes, prevents hospital readmissions, accelerates drug development, and closes critical gaps in care-ultimately making science smarter, healthcare simpler, and patients healthier.
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Leads design, implementation and interpretation of the global clinical program for a drug candidate to deliver a successful regulatory submission worldwide through regulatory submission and approval (i.e., Phase 2, 3, pediatric and interventional Phase 4 studies)Works closely with early development to ensure alignment between early and late stage development strategy.
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International Oncology Medical Affairs, Pfizer Research & Development (PRD) cross-TA global Medical platforms, Worldwide Medical, Drug Safety Research and Development and Safety in order to drive TA Medical Strategy across the organization.
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You will contribute to the development of an affiliate marketing strategy for each advertiser and ensure the successful execution of that strategy, including managing Client Partnerships Associates in their tactical execution.
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This is a Remote Role based in North America*Job OverviewProvide leadership and advice on the development of optimum regulatory strategies for drug development, product lifecycle management and portfolio management, particularly focused on emerging biopharmaceutical company customer goals in oncology.
$215,100 - $366,200 a yearFull-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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The Business Integration Specialist will work collaboratively with the Business owner and the rest of the business team to develop the strategy behind how each MES module will support the business requirements definition as well translation and specification of all functional requirements.
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Global BDO Strategy: Drive initiatives to enhance the harmonization and efficiency of drug development on a global scale, contributing to cost savings. Drug Development Strategy: Offer strategic input into development plans to ensure alignment with product profiles and regulatory expectations.
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Work closely with Marketing and Sales team in addition to other cross-functional leaders to build and execute an effective and efficient regulatory strategy for domestic and international levels, ensuring regulatory compliance for all new product development regarding chemical, formula, and packaging compliance for cosmetics and children’s products regulations.
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This role will be responsible for the development and execution of pricing analytics to drive profitable sales and revenue growth, while supporting overall corporate strategy. In order to be considered for this position candidates are required to submit an application for employment through our career site, be at least 18 years of age, willing to take a drug test, submit to a background investigation as part of the selection process, as well as additional periodic background checks as required by the Chemical Facility Anti-Terrorism Standards (CFATS) or regulations adopted by the department of Homeland Security or other regulatory agencies.
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The company is growing exponentially with a focus in drug development within the oncology space; this hire is purely due to growth. Our client, a Reputable, Global Pharmaceutical Company, is seeking a Regulatory Affairs Strategy professional at the Director level.
ExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Participation in NDA/MAA/Submission experienceTrack record and demonstrated ability to lead and manage both science and business aspects of drug development. The MDMP interacts and partners with marketed products R&D function leads (regulatory affairs, pharmacovigilance, global development operations and project management) to set R&D strategy and prioritize R&D functional support for assigned MP portfolio.
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Serve as a project management liaison with other groups within QPS.Provide consultation to clients on drug development process, strategy, and plans as needed. QPS’ Story:Since its inception, QPS has been assisting pharmaceutical, biotechnology and medical device companies with their drug development efforts by providing a full range of Neuropharmacology, DMPK, Toxicology, Bioanalysis, Translational Medicine, Early Phase Clinical and Phase II – IV Clinical Research services.
Full-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Cogent People Inc is looking for a full-time Business Development Executive to lead its business development (BD) efforts and develop the company’s BD strategy and be a part of its growth journey.
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Your primary role as M&Q Data Governance Lead is to co-create, execute, improve, and oversee Manufacturing and Quality (MQ) Data Strategy and Governance in collaboration with Business Data leaders.
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