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Job Categories: Advertising/Marketing/Public Relations, Arts, Entertainment, and Media, Banking, Biotechnology and Pharmaceutical, Consulting Services, Finance/Economics, Financial Services, Healthcare, Other, Healthcare, Practitioner and Technician, Information Technology, Internet/E-Commerce, Legal, Sales, Broadcasting/Communications, Research & Development, Medical, Web Technology.
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Minimum of 15 years of experience as a regulatory toxicologist (study director/monitor and/or project lead) in the pharmaceutical or biotechnology industry or within a regulatory authority. Minimum of 15 years of experience as a regulatory toxicologist (study director/monitor and/or project lead) in the pharmaceutical or biotechnology industry or within a regulatory authority.
$170,000 - $236,667 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Clinical data management experience in a medical device, pharmaceutical company, or similar environment (e.g., CRO); oncology, immunology, or complex disease therapeutic area is a must. Is accountable for inspection readiness of external data documentation filed/archived in Trial Master File (TMF) according to applicable Daiichi Sankyo and regulatory requirements.
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Prior experience in the pharmaceutical industry as a Publications Manager is preferred. 5+ years' relevant pharmaceutical/ biopharmaceutical industry experience. Whether you are considering starting a family, need help paying for emergency back up care or summer camp, looking for mental health resources, planning for your financial future, or supporting your favorite charity with a matching contribution, CSL Seqirus has many benefits to help achieve your goals.
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To help develop and deliver novel antibody therapies to patients, Genmab has formed 20 strategic partnerships with biotechnology and pharmaceutical companies. Requirements: BSc or MSc level degree preferably within the life sciences (PharmD, PhD, or MD preferred) Minimum of 10 years of experience within Regulatory Affairs (Oncology experience preferred) Direct interaction/negotiation skills with regulatory authorities (e.g. FDA, EMA) A broad knowledge of development and life-cycle management is preferred.
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Fluency with key pharmaceutical data sources and platforms such as IQVIA, MMIT, 852/867 Wholesaler data, Veeva CRM, and Power BI. Fluency with key pharmaceutical data sources and platforms such as IQVIA, MMIT, 852/867 Wholesaler data, Veeva CRM, and Power BI.
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The right person will be out of the Pharmaceutical, Pharmaceutical, Client, Sandoz, Sanofi, Bristol Meyers, Amerisource Bergan, Hershey, Unilever, IFF, Church & Dwight, L'Ore al, Este Lauder, Polo, level companies.
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10 or More Years Recent experience with government, trade association, think tank, or pharmaceutical company required. Daiichi Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and technology.
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Intermediate knowledge of pharmaceutical manufacturing and utilities that support cell therapy clinical. Intermediate knowledge of cGMP pertaining pharmaceutical facilities, utilities, and equipment.
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10 or More Years Pharmaceutical industry experience or commensurate healthcare or research experience required. Collaborates across GMA functions to develop, review, and align on key scientific communications and medical information response documents within legal and compliance regulations.
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A background of pharmaceutical manufacturing or quality control/quality assurance is a plus. Knowledge of US pharmaceutical regulations is essential. Job Title: CMC Regulatory Technical Writer II.
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This position will work directly with External Manufacturing Organizations (EMO) involving Pharmaceutical, Medical devices/Combination products, Consumer products /OTC and Biologics to ensure drug products/ Biologics are manufactured as per cGMP regulations and Bausch Health requirements.
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MHA provides expertise in Group Purchasing, Managed Care and Payer Contracting, Reimbursement Management, Specialty Pharmacy Solutions, Pharmaceutical Data Analytics, Consultant Pharmacy Software and Legislative Advocacy.
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Yearsof experience in strategic sourcing, indirect procurement, and/or supply chain management in pharmaceutical, medical device, or healthcare industries. Team Leadership: Provide leadership, guidance, and mentoring to a team consisting of Travel Agent, Supplier Diversity Manager, Analytics Manager, Analytics Analyst, and Buyer(s.
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5-7 years in the pharmaceutical industry, preferably with 1-3 years CMC regulatory experience. Participate in the development of the CMC regulatory strategy for small molecules, biologics and cell therapy submissions.
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