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1907 jobs

purposethe safety science medical Director in Licensing and early development (lead) safety will work under the supervision of a safety science group medical Director, be responsible for particular aspect(s) of an overall program or a group of .....
req id 41021 title medical science liaison, oncology - los angeles city los angeles state / province california country united states region north america company overview at lilly, we unite caring with Discovery to make life better for people .....
responsibilities about sanofisanofi, a global Healthcare Leader, discovers, develops and distributes therapeutic solutions focused on patients' needs. sanofi is organized into five global business units: Diabetes and cardiovascular, general .....
the snr medical Advisor provides comprehensive medical and scientific support for shire products in a specific therapeutic area within a local operating company (loc). primary responsibilities include scientific projects to design development and .....
serve as the field-based extension of the therapeutic area medical Strategy group hcp related activities expected to comprise 80% of msl responsibilities systematically identify the scientific exchange needs of key opinion leaders (kols), .....
this an exciting time to join a rapidly growing and dynamic arena, with a robust portfolio of assets across multiple Therapeutic Areas.  we are in search of a medical and scientific writer who will act as a subject-matter-Expert (sme) for the .....
req id 40935 title medical science liaison, Dermatology / Gastroenterology - atlanta city atlanta state / province georgia country united states region north america company overview at lilly, we unite caring with Discovery to make life better for .....
shire is the leading global Biotechnology company focused on serving people with rare diseases and other highly specialized conditions. we have best-in-class products available in more than 100 countries across core Therapeutic Areas including .....
job profilepreparation of development, quality and regulatory documents in Compliance with regulatory standards, e.g. mdd, cfr 820.duration: 6-8 months, potentially longer. (the project will be limited to 6-8 months, but can be extended depending on .....
the launch of amgen's 1st biosimilar, are you part of the team?in this role you will maximize amgen's biosimilars value propositions for amgevita (amgens first biosimilar) through first-class medical and scientific projects, services and expertise .....
1907 jobs

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