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Syneos Health
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Franklin, NJ
Responsibilities Youll join The Scientific and Medical Affairs Advisory Group within Syneos Health Consulting....
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2 hours ago
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Boston Biomedical
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Cambridge, MA
Clinical Practices, FDA regulations, ICH guidelines, and the drug development process....
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2 days ago
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Celgene Corporation
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Summit, NJ
Reporting to the Associate Director, Global Drug Safety & Risk Management (GDSRM), Aggregate Safety Reporting (ASR), the primary role of the ASR Sr Manager, Medical Writer is to provide formatted Periodic...
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18 hours ago
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Artech Information Systems L.L.C.
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Mounds View, MN
Clinical Evidence Specialist Position Description The Clinical Evidence Specialist plans and develops clinical evaluation reports (CERs) and related evidence deliverables for cardiac medical...
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7 hours ago
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Cambridge, MA
Sr Medical Writer Return to previous page Friday, november 15, 2019 Description job summary: As the world's largest staffing and recruitment agency in the world, we can commit to find you the perfect...
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1 day ago
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Townsend & Associates
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Trenton, NJ
In-depth knowledge of AMA Medical Writing Style, Good Clinical Practices, FDA regulations, and the pharmaceutical development process, including translational medicine data generation....
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4 days ago
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Cambridge, MA
job summary: As the world's largest staffing and recruitment agency in the world, we can commit to find you the perfect role that gives you the opportunity to learn and grow in the life sciences...
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5 days ago
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Artech Information Systems LLC
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Lawrence Township, NJ
Regulatory & Medical Affairs - Medical Writer Location : Princeton Pike , NJ Duration : 12 Months Oncology Medical Writer and Project Manager [Biomarkers, translational medicine, and pharmacodiagnostics...
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5 days ago
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Psi Intl., Inc.
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Fairfax, VA
Biomedical consulting firm is currently seeking a Medical Writer to join our Bethesda, MD team....
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6 days ago
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Pfizer
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Collegeville, PA
Senior Medical Writer (Senior Manager) in Collegeville , Pennsylvania Reference #: 4769809ROLE SUMMARYThe Senior Medical Writer is a member of the Clinical Communications team within the Medical Writing...
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6 days ago
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Mms Holdings
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Philadelphia, PA
Clinical Practices, and ICH guidelines a plus Substantial clinical study protocol experience, as lead author, required Experience leading and managing teams while authoring regulatory documents with...
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7 days ago
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Custom Learning Designs, Inc
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Belmont, MA
Senior Medical Writer If you thrive in an intellectually stimulating environment where you can combine your love for writing with your medical and scientific knowledge by creating training materials...
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8 days ago
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AbbVie
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North Chicago, IL
Mentor and provide guidance to medical writers. Provide writing- and process-related mentorship/training to new medical writers across TAs....
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8 days ago
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Mms Holdings
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Canton, MI
Clinical Practices, and ICH guidelines a plus * Substantial clinical study protocol experience, as lead author, required * Experience leading and managing teams while authoring regulatory documents...
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9 days ago
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Merck & Co., Inc.
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Rahway, NJ
Our Medical Writers are integral to helping bring medical breakthroughs to the world. We rely on expert skills and inventiveness to realize this life-saving goal....
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11 days ago
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This class is offered as CS6440 at Georgia Tech where it is a part of the Online Masters Degree (OMS). Taking this course here will not earn credit towards the OMS...
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