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imove, the sanofi vie program, is available to citizens of the european economic area (eu + norway, liechtenstein and iceland) aged between 18 and 28.please note that since this program is primarily an international development program, candidates .....
solvay is a multi-specialty chemical company committed to developing Chemistry that addresses key societal challenges. we innovate and Partner with customers in diverse global end markets. solvay composite materials combines 50 years of technology .....
primary location:  toronto (canada) or gothenburg (sweden)role purpose:  the Clinical Trial safety management (ctsm) Scientist will work under the supervision of the ctsm program lead, senior ctsm Scientist to assist in Clinical Development .....
responsibilities department descriptionthe Health safety & environment group (hse) is responsible for implementing programs and policies that comply with all local, state and federal hse rules and regulations and continuously strive to reduce the .....
teva is a global Pharmaceutical Leader and the world’s largest generic medicines producer, committed to improving Health and increasing access to quality Health solutions worldwide.  our employees are at the core of our success, with .....
at astrazeneca we work together across global boundaries to make an impact and find answers to challenges. we do this with the upmost integrity even in the most difficult situations because we are committed to doing the right thing. we continuously .....
job description we are expanding iqvia's Epidemiology and Drug Safety team and are seeking outstanding additions to our team.about our teamthe Epidemiology and Drug Safety practice of ims Health is a fast-growing component of the medical/scientific .....
bristol-myers squibb is a global biopharmaceutical company whose mission is to discover, develop and deliver innovative medicines that help patients prevail over serious diseases.one shared journey is moving us forward at bristol-myers squibb. .....
descriptionresponsible for receipt of all marketed and investigational product reports of Adverse Events from all sources. preliminary evaluation of all Clinical Trial, spontaneous (post-Marketing), and solicited reports of Adverse Events, including .....
job description senior (regulatory) safety/Pharmacovigilance Expert to join an expanding team of senior experts in tarius (on-line platform). your role:you will join a dedicated and experienced team of senior regulatory experts who together with the .....
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