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Post-approval RA Project Manager - International Markets Regulatory Affairs - Israel
Teva pharmaceutical 7
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 colleagues .....
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. .....
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. .....
Regulatory and Start Up Specialist / Senior Site Management Coordinator - office based in Vilvoorde - (1807488)
Iqvia 29
job description join us on our exciting journey!iqvia™ is the human Data Science company™, focused on using data and science to help Healthcare clients find better solutions for their patients. formed through the merger of ims Health and .....
Regulatory and Start Up Specialist / Senior Site Management Coordinator - office based in Vilvoorde - (1807488)
Iqvia 23
job description join us on our exciting journey!iqvia™ is the human Data Science company™, focused on using data and science to help Healthcare clients find better solutions for their patients. formed through the merger of ims Health and .....
Regulatory Information Management- SPECIALIST - United Kingdom, United States
Navitas Life Sciences 72
category: senior level location: uk (portsmouth) or us(princeton) job type: full time Education: minimum 10 years in industry experience in a regulatory Operations Leadership role in rim space – with Consulting experience job description: position .....
pursuant to section 20 c.f.r. 656.10, you are hereby notified that an application for alien employment certification has been filed by shire human genetic therapies inc. for the following job opportunity: job location: lexington, ma position: .....
your job preparation of electronic Applications in particular in the eCTD format for approval according to the requirements of the relevant authorities (europe, usa, etc.) including preparation of proposals, Project Planning and tracking .....