Job DescriptionThis position involves preparing scientific and regulatory documents on behalf of government clients for submission to the Food and Drug Administration FDA Investigational New Drug ...
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Job DescriptionThis position involves preparing scientific and regulatory documents on behalf of government clients for submission to the Food and Drug Administration FDA Investigational New Drug
Were seeking a highly motivated selfdriven and enthusiastic Regulatory Affairs writer to join our Regulatory Affairs Team At RemeGen our regulatory affairs group is responsible for drafting and re ...
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Were seeking a highly motivated selfdriven and enthusiastic Regulatory Affairs writer to join our Regulatory Affairs Team At RemeGen our regulatory affairs group is responsible for drafting and re
MMS is an awardwinning datafocused CRO that supports the pharmaceutical and biotech industries with a proven scientific approach to complex trial data and regulatory submission challenges Strong ...
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MMS is an awardwinning datafocused CRO that supports the pharmaceutical and biotech industries with a proven scientific approach to complex trial data and regulatory submission challenges Strong
Medical WriterSupernus Pharmaceuticals Inc
Rockville, MD
This position will lead the medical writing activities for multiple programs within Clinical Research Individual will be reviewingwriting clinical documents in support of Phase 14 clinical studies ...
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This position will lead the medical writing activities for multiple programs within Clinical Research Individual will be reviewingwriting clinical documents in support of Phase 14 clinical studies
Medical WriterAccreditation Council for Graduate Medical Education ACGME
Chicago, IL
Position Overview The Sr Medical Writer is responsible for the development and creation of highquality scientific communications materials for presentation and publication in scientific peer ...
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Position Overview The Sr Medical Writer is responsible for the development and creation of highquality scientific communications materials for presentation and publication in scientific peer
The Principal Medical Writer will be responsible for authoring and revising clinical and regulatory documents for submission to the FDA and other agencies and may also lead other internal and ...
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The Principal Medical Writer will be responsible for authoring and revising clinical and regulatory documents for submission to the FDA and other agencies and may also lead other internal and
Prior medical technical writing experience within the biotechpharmaceuticalCRO realm Experience and significant participation in preparation of clinical documents for regulatory submissions eg ...
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Prior medical technical writing experience within the biotechpharmaceuticalCRO realm Experience and significant participation in preparation of clinical documents for regulatory submissions eg
Director Medical Writing Reports to Head of Clinical Operations Overview Of Position Reporting to the Head of Clinical Operations the Director Medical Writing is responsible for providing ...
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Director Medical Writing Reports to Head of Clinical Operations Overview Of Position Reporting to the Head of Clinical Operations the Director Medical Writing is responsible for providing
The DirectorAssociate Director Medical Writing is responsible for leading clinical regulatory medical writing activities that conform to domestic andor international regulatory submission This ...
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The DirectorAssociate Director Medical Writing is responsible for leading clinical regulatory medical writing activities that conform to domestic andor international regulatory submission This
REMOTE Technical Writer We are currently seeking a seasoned Technical Writer for a 7 monthmedical condition genetic information mental and physical disability political affiliation ...
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REMOTE Technical Writer We are currently seeking a seasoned Technical Writer for a 7 monthmedical condition genetic information mental and physical disability political affiliation