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As a top five CRO, we have worked on 100+ marketed drugs across several therapeutic areas and conducted the pivotal or supportive trials that led to FDA and/or international regulatory approval of 45+ such drugs. At PRA Health Sciences, .....
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, .....
When you join PRA Health Sciences, you will not only witness the future of clinical development. You come to shape it!Do you have experience and great affinity with scientific writing? Do you see transforming data into an understandable text as a .....
Participates as a member of the PRA medical investigator team. Participates and assists in managing the screening process and clinical care of potential volunteers and study participants for clinical trials in the Phase I clinic. The position .....
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 .....
descriptionthe senior Medical Director/executive Medical Director, Clinical research will provide direct support as a subject matter Expert to various compounds & programs related to the sleep disorders therapeutic area. dependent upon specific .....
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 Director of global medical information and medical review leads the development and transfer of intellectual capital that maximizes the safe and appropriate use of alexion products to Healthcare professionals and patients .....
    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 .....
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