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You’re looking for Pharmacovigilance jobs in Cambridge United States. On BrightOwl, we centralise vacancies from biotech, pharma and life sciences companies in general. Register for free, build your profile so that companies can contact you for new openings.

70 jobs

    position summary the Medical Director, Risk Management Pharmacovigilance is accountable for executing the safety and Risk Management activities for one or more assigned Clinical Development projects or marketed products to enable the safe and .....
responsibilities 60% execution of Pharmacovigilance system audit plan manage and conduct audit activities associated with Pharmacovigilance and Clinical Trial safety.  ensures the appropriate corrective and preventative actions are completed in .....
job description the company: sarepta therapeutics, headquartered in cambridge, massachusetts, is a commercial-stage biopharmaceutical company focused on the Discovery and development of unique RNA-targeted therapeutics for the Treatment of rare .....
amgen is seeking a Director Pharmacovigilance Operations to work out of their thousand oaks, ca or cambridge, ma location.the Director Pharmacovigilance Operations ensure that Pharmacovigilance (pv) Operations safety systems and processes fulfill .....
karyopharm therapeutics is a Clinical-stage Pharmaceutical company focused on the Discovery and development of novel first in-class drugs directed against nuclear transport targets for the Treatment of Cancer and other major diseases. summary: the .....
summary: primary responsibility is oversight of processing of Adverse Events and safety data to ensure Compliance with worldwide regulatory requirements, as well as adherence to internal procedures and contractual requirements with business .....
the head of Pharmacovigilance Operations is accountable for day-to-day efficient and compliant global Pharmacovigilance operational management and oversight groups responsible for case management activities performed internally and externally by .....
amgen is seeking a global safety manager to function as a global Pharmacovigilance (pv) Scientist at its cambridge, ma location to join the global Patient Safety & labeling (gps&l) group. the global pv Scientist will report to the global .....
    position summary this position is accountable for the timely preparation of high quality, regulatory-compliant Clinical document deliverables for alexion. this position will lead the Medical writing (mw) activities across a disease area or set .....
the purpose of the position is to prepare corporate, us and eu labeling (prescribing information and patient information) documents for developmental, mature and marketed products of the sanofi-genzyme portfolio ( products in rare diseases, .....
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