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In collaboration with the Clinical Affairs Lead and Medical/Scientific Lead, prepares strategy decisions, presents, and discusses data at relevant team, governance, external consultants, KOL and potentially regulatory meetings.
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To become a Product Tester, you'll start with a pre-qualification phase conducted by two leading consumer research companies. During your application process, reputable market research companies will determine your demographics and consumer profile to establish what products would be suitable for you to test.
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Leads engagement with internal key stakeholders (e.g. Global Medical Affairs, MCE, Region/LOCs, MPD, Global Outcomes Research and Epidemiology [GEO], and Publications) as needed. The Associate Director, Global Scientific Communications, Mature Brands, is a dynamic, strategic role within Global Medical Affairs that collaborates with cross-functional partners to own one or more disease areas / assets on a Global level.
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This ensures a perfect match between your consumer profile, demographics, and the testing opportunities available. If you are a manager, receptionist, warehouse or factory worker, driver, medical assistant, nurse, cleaner, college student, messenger, maid, teacher, retail associate, salesperson, secretary, server, janitor, cashier, contract worker, or intern who is looking for a flexible part-time or seasonal job, you should try paid Product Testing to supplement your income.
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Independently manage all aspects of R&D assay validations, experiments, data analysis, sponsor updates, interact with Scientific Affairs, IT, operational las, business development, and project management teams.
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The primary role of the Director, Regulatory Affairs - CMC is to create and/or manage contributions from others for CMC regulatory submission documents. This position reports directly to the Senior Director, Head of Regulatory Affairs - CMC. The Director, Regulatory Affairs - CMC will be responsible and accountable for CMC submission documents while successfully up-holding the vision for the function and help mentoring junior team members.
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You will be providing confidential administrative departmental support to members of the Scientific Affairs Leadership team, and to ensure that administrative processes run smoothly. Department: Scientific Affairs Leadership team/Administration.
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Work closely with Global Patient Safety and Risk Management (GPSRM), Clinical Research, Regulatory Affairs, Clinical Operations, Biostatistics, and Medical Affairs to inform clinical development and real-world outcomes and answer product- and disease-area research questions for Alnylam RNAi therapeutics using observational studies, EMR/claims data, and RWE. The Senior Director, Epidemiology reports directly to the Senior Vice President, Data Science, Statistics, and Epidemiology.
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They collaborate with faculty, the HMS Dean for Clinical and Academic Affairs, and others in the HMS Dean’s Office to achieve these objectives in supporting gender equity and positive faculty experience through development and implementation of programming that includes a focus on community building, mentoring and leadership training, and promoting the visibility and interests of women in science.
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Partner with Global Clinical and Medical Affairs, Marketing, and Market Access teams to execute strategic HEOR activities to support the successful market access and adoption of Philips devices and solutions.
$153,216 a yearFull-timeExpandApply NowActive JobUpdated 19 days ago - UpvoteDownvoteShare Job
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This group advises clients within Healthcare & Life Sciences; Energy; Advanced Manufacturing & Mobility; Private Equity; Technology, Media & Entertainment, and Technology; Consumer Products & Retail; Government & Public Sector; and Financial Services sectors.
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Primary Responsibilities:This role involves working closely with scientists and regulatory affairs departments on various nonclinical regulatory documents. The Scientific Editor's responsibilities will be:Collaborate with scientists on nonclinical regulatory documents such as Investigator Brochures, Nonclinical Study Reports, Annual Reports, CTAs, INDs, and NDAs. Assume lead scientific writing responsibility on projects, utilizing regulatory and publication documentation expertise.
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A thorough understanding of global drug development functional areas including preclinical, clinical, regulatory affairs and manufacturing. Knowledge of GLP/GCLP and GCP global regulatory requirements for clinical trial submissions (USA, UK & EU), understanding of 21CFR Pt. 11 with respect to clinical systems (QMS.
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This role will report to the Senior Vice President, Global Value, Access, Public Policy and Government Affairs. This role is responsible for leading the HEOR development and execution of the global evidence teams, engaging closely with and guiding the product development teams across our pipeline, supporting our regions and affiliates, as well as leading our V&A engagement with external stakeholders on evidence and access.
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About youAdvance degree in life sciences or pharmaceutical sciences (PhD, PharmD, MD) with significant years of relevant medical affairs experience. You should have experience and a proven track record of success in the biotechnology or pharmaceutical industry managing teams, with a strong background in scientific research, publication planning, medical communications, and medical affairs activities.
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consumer affairs jobs Title: regulatory in Cambridge, Anoka, Minnesota
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