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We are seeking a highly skilled Senior Cost Manager to join our finance team and play a pivotal role in managing and optimizing the cost structure of our biopharmaceutical manufacturing operations.
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Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies. Develop and enforce operational standards for biomarker management, vendor relations, and internal processes to ensure program quality, efficiency, and regulatory compliance.
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A concentration in biopharmaceutical market access, field reimbursement or managed markets is preferred. All responsibilities of the Associate Director will be carried out with strict adherence to the JJIM Credo and HCC Guidelines, in line with the FRM Rules of Engagement.
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Join our game-changing, global company dedicated to creating better, smarter, faster ways to get biopharmaceutical therapies to patients. 3+ years in Pharmaceutical or Life Science sales. Join our game-changing, global company dedicated to creating better, smarter, faster ways to get biopharmaceutical therapies to patients.
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Proficiency in using at least one major Clinical Data Management System (e.g., Medidata, OCRDC, Inform, etc. Approve all data management documentation, including CRF, data validation plans, and others, ensuring compliance with DMP and quality standards.
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Additionally, certain local governments or Syneos Health customers may have vaccine requirements that apply to some of our employees. Syneos Health complies with all applicable federal, state, and municipal paid sick time requirements.
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Prior knowledge of genomic medicine approaches, biopharmaceutical manufacturing process flow, and GMP. Experience working with large biopharma organizations; launching and scaling new solutions offerings in an emerging market.
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B.A. or B.S. degree (preferably in Engineering or Life Science) and at least two years' experience in the pharmaceutical or biopharmaceutical industry, or an equivalent combination of education and experience.
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Assist in the integration of the risk management program with quality systems including, but not limited to, Validation, CAPA, Change Control, APQR, Complaints, and Inspection Readiness. Software that will be used in the role: eValRoche, VeevaVault and one QMS.
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Responsibilities: or degree (preferably in Engineering or Life Science) and at least two years of experience in the pharmaceutical or biopharmaceutical industry, or an equivalent combination of education and experience.
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Syndax Pharmaceuticals is a clinical stage biopharmaceutical company developing an innovative pipeline of cancer therapies. Minimum 5+ years of previous pharmaceutical, biotech, and/or medical sales experience with a strong preference for Oncology/Hematology.
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Job Title: Quality/Validation Engineer. Working with multiple functions, lead solution of validation issues following cGMP regulations and standards. Review and approve validation documents (e.g. Project Plans, User Requirements, Protocols, Validation Deviations, Summary Reports, etc) for CGMP and technical content.
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Jazz Pharmaceuticals plc (NASDAQ: JAZZ) is a global biopharmaceutical company whose purpose is to innovate to transform the lives of patients and their families. Reporting to the Executive Director of Tax, this position will be responsible for various tax issues, including income tax provision, preparation/review of tax returns, audit defense, and various other tax projects.
$148,000 - $194,250 a yearFull-timeRemoteExpandUpdated 1 month ago
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