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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 .....
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 .....
quality risk lead (manager level)job description:key role to achieve corporate and departmental strategic and operational goalsis a Member of the pv quality Leadership team to set the vision for the global department and local pv activities .....
key contributions & activities:ensure consistent and effective Quality System for GXP and Health-regulated activities is implemented for medical activities, in Compliance with applicable regulations, global quality Policy and company quality .....
the Associate Medical Director – safety is responsible for global Pharmacovigilance (pv) for marketed and/or investigational products, including review and Analysis of safety data from post-Marketing sources and from Clinical trials, the .....
 Director, pv science overviewalnylam was founded in 2002 on a revolutionary vision and bold mission which remain firmly in place today. we are leading the Translation of RNA interference (rnai) into a new class of innovative medicines .....
Clinical research Director, Neurology developmentsome of the Clinical research Director’s (crd) core job responsibilities include those listed below, as well as all other duties assigned.scientific and technical expertise:has and maintains deep .....
    position summary the senior manager, safety Scientist plays a pivotal role within global Pharmacovigilance to ensure safety assessment for all alexion products, in close collaboration with the product assigned global medical safety .....
    position summary responsible and accountable for all aspects related to the handling of safety information originating from post-Marketing, Clinical trials, literature, and other sources. investigation, Documentation, Medical Research, and .....
responsibilities key contributions & activities:ensure consistent and effective Quality System for GXP and Health-regulated activities is implemented for medical activities, in Compliance with applicable regulations, global quality Policy and .....
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