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    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 .....
 Clinical Trial manager 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 .....
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 .....
Clinical Informatics, Associate Director   overview   alnylam 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 .....
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 .....
key responsibilities:  the Clinical research Director is playing a role among a group of physicians and scientists across the entire oncology portfolio of compounds.  this may include: leading a segment of the clinical program (resource .....
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 .....
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