• SGS North America (Germantown, MD)
    …network of over 2,000 offices and laboratories around the world.Job Description SUMMARY The Associate Director Clinical Operations US ( Associate Director ... Operations' staff including administrative, budgetary, resource and performance management. The Associate Director CO US develops and implements strategic… more
    CareerBuilder (09/18/20)
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  • Analysts (Summit, NJ)
    …review the job description below:Key Responsibilities:Job Title: Associate Director (Consultant, Global Regulatory CMC Biologics/Cell Therapy)Job ... ACS group has an immediate need for a CONSULTANT, GLOBAL REGULATORY CMC BIOLOGICS/CELL THERAPY with experience in the any Industry. This is a 6+ months contract… more
    CareerBuilder (09/18/20)
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  • Bristol Myers Squibb (Seattle, WA)
    …touch to every treatment we pioneer. Join us and make a difference. Come join our Global Cell Therapy Project Management team In this role, you will be focused on a ... of these projects will range from small to medium complexity with supervision from the global project manager in support of the Global Project Team Location of… more
    jobrapido (09/30/20)
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  • Bristol Myers Squibb (Seattle, WA)
    …results. Position Summary We are seeking a Principal Product Quality Lead (Principal PQL), Associate Director of Global Product Quality. The Principal PQL ... Summit, NJ or Seattle WA and reports to the Director , Global Product Quality, Cell Therapy Vector...technical quality expertise and compliance oversight in accordance with global regulatory requirements and internal policies in… more
    jobrapido (09/30/20)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …structure-guided R&D center in Berkeley, CA. Job Summary: This position serves as the Regulatory Affairs (RA) CMC project representative to the CMC sub team and the ... team and serves as ad hoc member to the Global Project Team for late stage projects. This position...& variations (eg, NDA, BLA, MAA). This position authors regulatory documents where necessary with supervision. This position conducts… more
    CareerBuilder (08/18/20)
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  • Bristol Myers Squibb (Princeton, NJ)
    Bristol-Myers Squibb is a global Biopharma company committed to a single mission: to discover, develop, and deliver innovative medicines focused on helping millions ... applying analysis and reporting standards, and driving compliance with regulatory requirements, corporate and departmental SOPs and work practices Drives… more
    jobrapido (09/30/20)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …for cardiovascular diseases, under the Group's 2025 Vision to become a " Global Pharma Innovator with Competitive Advantage in Oncology," Daiichi Sankyo is primarily ... of pharmacometrics models, PK/biomarker data, derived analysis-ready data files, regulatory guidelines pertaining to M&S, and programming and analytical software.… more
    CareerBuilder (09/30/20)
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  • Careerbuilder-US (Tampa, FL)
    …readily-available for meaningful guidance and support. In addition to the Managing Director and Benchmark Internationals' global brand, the Tampa Transaction ... such, is looking for an experienced and driven Transaction Director to take over an M&A deal team. The...Be able to obtain a Florida real estate sales associate license within 60 days of employment. . Have… more
    CareerBuilder (09/01/20)
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  • Alpha Consulting (Madison, NJ)
    …in the scope of the assigned development project(s), the Associate Director , Clinical Development may have global or regional responsibilities and fulfil ... ASSOCIATE DIRECTOR WITH CLINICAL DEVELOPMENT EXPERIENCEMADISON,...activities in compliance with all relevant laws, regulations, and regulatory guidelines as well as all the Client's policies… more
    CareerBuilder (09/13/20)
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  • SRG Woolf (Madison, NJ)
    Associate Director , Clinical DevelopmentThe Associate Director , Clinical Development should expect to be asked to participate in internal process ... focus on efficient and timely solutions. He/she leads the development of the Global Development Strategy, in collaboration with the Core Team and other applicable… more
    CareerBuilder (09/18/20)
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  • CSL Plasma (Shanghai City, IL)
    …DescriptionAs a key member of the Greater China Medical Affairs team, the Associate Director , Medical Affairs will provide short and long-term strategic ... is the parent company of CSL Behring and Seqirus. CSL Behring is a global leader in the protein biotherapeutics industry, focused on bringing to market biotherapies… more
    CareerBuilder (09/18/20)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …for cardiovascular diseases, under the Group's 2025 Vision to become a " Global Pharma Innovator with Competitive Advantage in Oncology," Daiichi Sankyo is primarily ... at each phase of the development are scientifically sound, can fulfill regulatory requirements and deliver the pre-specified product profile.CRO / Vendor Oversight:… more
    CareerBuilder (09/26/20)
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  • Integrated Resources, Inc (Cambridge, MA)
    …frames dictated by regulatory authorities.5. If applicable, manage Associate Medical Director (s) overseeing their activities for assigned compounds/products ... within Client, external stakeholders in the medical community as well with global regulatory authorities.1. Manage safety surveillance for assigned compounds /… more
    CareerBuilder (09/27/20)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …diseases, heart and kidney diseases, and other rare diseases. Job Summary:The Director / Associate Director , Global Medical Affairs Oncology ... disorders, under the Group's 2025 Vision to become a " Global Pharma Innovator with a Competitive Advantage in Oncology,"...5 years of Medical Affairs experience, preferably as an Associate Director ; 8 years of professional medical… more
    CareerBuilder (09/01/20)
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  • Collabera (Irvine, CA)
    ndustry Pharma-Location Irvine CAJob Title Associate Director R&D PMJob Requirements:Main Areas of Responsibilities Drive and support department initiatives ... and the interdependencies of individual development activities. Working knowledge of regulatory requirements for product registration on global basis. Expert… more
    CareerBuilder (09/18/20)
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  • TSYS (Columbus, GA)
    Every day, Global Payments makes it possible for millions of people to move money between buyers and sellers using our payments solutions for credit, debit, prepaid ... your mark on the payments technology landscape of tomorrow. Global Payments is the parent company for TSYS, Netspend,...operational value and quality of service. Ensures compliance with regulatory and audit standards set forth by the Statement… more
    CareerBuilder (09/18/20)
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  • SGS North America (West Chester, PA)
    …over 2,600 offices and laboratories around the world.Job Description In general, the Associate Director of Biopharmaceutical Services is expected to be highly ... testing and certification company. SGS is recognized as the global benchmark for quality and integrity. With more than...release and characterize all types of biological therapeutics. The Associate Director will also have experience in… more
    CareerBuilder (09/03/20)
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  • Scotiabank (New York, NY)
    …of Scotiabankers to help customers become better off. In this role as Quality Control, Associate Director , you will manage and assist in the review and approval ... parties. Is this role right for you? * Conduct the regulatory review of onboarding of US Global Banking and Markets clients in an efficient, compliant and… more
    ScotiaBank (09/28/20)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …for cardiovascular diseases, under the Group's 2025 Vision to become a " Global Pharma Innovator with Competitive Advantage in Oncology," Daiichi Sankyo is primarily ... complexity in design and geographic scope). Prepares clinical section of regulatory document. Collaborates as team member with AROs/CROs. Drafts development plans,… more
    CareerBuilder (09/19/20)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …quality, and develop medical writing timelines, processes, and working standards. The Associate Director , Medical Writing will possess advanced knowledge of ... for cardiovascular diseases, under the Group's 2025 Vision to become a " Global Pharma Innovator with Competitive Advantage in Oncology," Daiichi Sankyo is primarily… more
    CareerBuilder (09/01/20)
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