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Responsible for performing medical review for any or all of the following according to the client Standard Operating Procedures and guidelines: review of aggregate reports (e.g. Periodic Safety Update Reports (PSURs), Periodic Benefit Risk .....
Responsible for performing medical review for any or all of the following according to the client Standard Operating Procedures and guidelines: review of aggregate reports (e.g. Periodic Safety Update Reports (PSURs), Periodic Benefit Risk .....
req id 43625 title us regulatory Advertising and promotion Medical Device Reviewer city indianapolis state / province indiana country united states region north america workplace arrangement local company overview at lilly, we unite caring with .....
purpose:serves as a therapeutic area (or multiple ta), primary point of contact for externally sponsored and affiliate-run Research (iis and collaborative study) Operations in global medical affairs. acts as the subject matter Expert for the review, .....
other locations:us- nj- summit eastcelgene is a global biopharmaceutical company leading the way in medical Innovation to help patients live longer, better lives. our purpose as a company is to discover and develop therapies that will change the .....
description summary:this position is for Medical Director within the enfortumab vedotin program, an antibody drug conjugate currently in late phase development for metastatic urothelial Cancer and earlier phase development for other solid tumors. .....
    Position Summary The Associate Director of Global Medical Information and Medical Review is responsible for managing all US and Global Medical Information service functions within a given therapeutic area, including but not limited to the .....
    Position Summary The Sr. Manager of Global Medical Information and Medical Review will sustain and promote Alexion’s professional standing and integrity amongst patients, health care professionals and the pharmaceutical / biotech .....
    Position Summary  The Director of Medical Coding and Clinical Data Review in the Global Clinical Data Management (GCDM) department is responsible for the development of a medical coding and clinical data review sub-department developing a new .....
the Translational Medicine Leader (tml) oncology is a core Member of the well-established oncology Translational Medicine group. the tml leads the exploratory medicine Strategy for early oncology drug assets. he/she is the key medical .....
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