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Daiichi Sankyo jobs - Morristown, NJ

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  • Associate Director, Regulatory Affairs

    Daiichi Sankyo - Edison, NJ

    of IND’s and NDA’s for development practices. Represent Daiichi Sankyo’s regulatory group in internal and external ... ways and norms. Willing to travel 20% of the time. Daiichi Sankyo, Inc. is an Equal Opportunity Employer -...

    1 day ago from job.com

  • Quality Assurance Intern

    Daiichi Sankyo - Edison, NJ

    Daiichi Sankyo, Inc., is an equal opportunity/affirmative action employer. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national...

    7 hours ago from IHispano

  • Associate Director Clinical Pharmacology

    Daiichi Sankyo - Edison, NJ

    years industry experience, or equivalent experience Daiichi Sankyo, Inc., is an equal opportunity/affirmative action employer. All qualified applicants will receive consideration for employment without regard to sex, gender identity,...

    7 hours ago from Women's Career Channel

  • Ass Dir Regulatory Operations

    Daiichi Sankyo - Edison, NJ

    Auto req ID 7174BR Job Title Ass Dir Regulatory Operations Functional Area Research & Development City Edison State New Jersey Job Description Job Description: The Associate Director, Regulatory Operations, within the Regulatory Operations...

    30+ days ago from Professional Diversity Network

  • Sr Director Clinical Safety

    Daiichi Sankyo - Edison, NJ

    Daiichi Sankyo is an Equal Opportunity Employer - Minority/Female/Disabled/Protected Veteran Auto req ID: 7291BR Job Title: Sr Director Clinical Safety Functional Area: Research & Development City: Edison State: New Jersey Job Description:...

    14 days ago from HealthJobsNationwide

  • Director Regulatory Affairs

    Leading Pharmaceutical Company - Edison, NJ

    activities. 4.Collaborate with all disciplines within the Daiichi Sankyo organization to obtain and/or provide information/data for regulatory filings. 5.Mentor/instruct and provide guidance to direct reports. 6.Review and interpret...

    18 days ago from IvyExec

  • Sr Clinical Study Mgr - Oncology

    Daiichi Sankyo - Edison, NJ

    of the supervisor. Coordinate and liaise with Daiichi Sankyo QA on audit activities * Provide oversight of the ... of trial and site level documents to the Daiichi Sankyo Document Control Center (DCC) in support of the Trial...

    14 days ago from HealthJobsNationwide

  • Manager, Quality Assurance - GMP

    Daiichi Sankyo - Edison, NJ

    GMP[DJ1] compliant drug products and services to Daiichi Sankyo'™s commercial markets and clinical study sites. This ... in accordance with FDA requirements and Daiichi Sankyo SOPsParticipate as a team member of the Daiichi Sankyo...

    1 day ago from job.com

  • Associate Director, Regulatory Affairs

    Leading Pharmaceutical Company - Edison, NJ

    strategies and strategic RACMC advice. Represent Daiichi Sankyo during FDA interactions; schedule and lead meetings with FDA CMC staff and prepare company personnel for FDA interactions. Determine the content for regulatory submissions as...

    17 days ago from IvyExec

  • Sr. Director, Experimental Medicine

    Daiichi Sankyo - Edison, NJ

    in Oncology; qualified to hold a US-state medical license. Cultural sensitivity and ability to influence outside of formal reporting lines.Must be willing to travel 20%25%20of the time Daiichi Sankyo, Inc. is an Equal Opportunity Employer...

    30+ days ago from Professional Diversity Network

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