Pharmaceutical Document Management Jobs
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Found 56 jobs
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Regulatory Specialist (Document Control - CMC & Bioanalytical)
Regulatory Specialist (Document Control - CMC & Bioanalytical) Our client, a growing innovator in the biopharma industry, is seeking a Regulatory D...
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Principle Medical Writer
Summary: The Principle Medical Writer is responsible for clinical regulatory documents (e.g., study protocols, Investigator Brochures, Clinical Stu...
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Senior Submission Manager
Wallingford TransitionBristol-Myers Squibb is a global biopharmaceutical company whose mission is to discover, develop and deliver innovative medicine
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Research Investigator- Protein Analytics and Characterization
Bristol-Myers Squibb At Bristol-Myers Squibb, we're creating innovative medicines for patients who are fighting serious diseases. We're also nurturing
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Research Investigator, Toxicology
Bristol-Myers Squibb is a global biopharmaceutical company whose mission is to discover, develop and deliver innovative medicines that help patients p
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Senior Stability Consultant
As a member of the Bulletproof family, you'll enjoy a culture that values diversity in all things - people, work, experience levels, and much more. We
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Research Investigator II
Responsibilities:Responsible for route scouting and the design and implementation of safe, efficient and robust chemical processes for the synthesis o
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Research Investigator I/II (Cancer Genetics Focused)
The Research Investigator will join the Immuno Oncology Resistance Biology research team at Bristol-Myers Squibb (BMS) in Cambridge, MA. This team is
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Research Investigator
We are seeking a highly motivated and innovative scientist to drive the development and implementation of immunoassays broadly supporting multiple the
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II-ON Research Liaison
Bristol-Myers Squibb is a global biopharmaceutical company whose mission is to discover, develop and deliver innovative medicines that help patients p
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Associate Director, Regulatory Operations
The Regulatory Operations Associate Director will be responsible for overseeing operational aspects of all regulatory submissions.
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Director Regulatory Affairs, CMC - Innovative Gene Therapy Start Up
DESCRIPTION Location: Menlo Park (US) Reporting to: Sr VP, Quality Assurance and Regulatory Affairs Orchard Therapeutics is an international biotec...
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Research Fellow
The successful candidate should have a PhD in organic chemistry, or a related field, with approximately 14 or more years of additional industrial or a
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PVA Manager, External Affairs
Bristol-Myers Squibb is a global biopharmaceutical company whose mission is to discover, develop and deliver innovative medicines that help patients p
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Associate Submission Manager
allingford TransitionBristol-Myers Squibb is a global biopharmaceutical company whose mission is to discover, develop and deliver innovative medicines
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Associate Submission Manager
Job DescriptionBristol-Myers Squibb is a global biopharmaceutical company whose mission is to discover, develop and deliver innovative medicines that
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Senior Submissions Manager
Wallingford TransitionBristol-Myers Squibb is a global biopharmaceutical company whose mission is to discover, develop and deliver innovative medicine
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Senior Submission Manager
Wallingford TransitionBristol-Myers Squibb is a global biopharmaceutical company whose mission is to discover, develop and deliver innovative medicine
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Senior Submission Manager
Wallingford Transition:Bristol-Myers Squibb is a global biopharmaceutical company whose mission is to discover, develop and deliver innovative medicin
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Associate Director, Submission Management
Wallingford TransitionBristol-Myers Squibb is a global biopharmaceutical company whose mission is to discover, develop and deliver innovative medicine