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C.G. (Carlisle, MA)

Scientific project management and clinical operations professional with 10+ years of clinical and quality control experience for both small and large international biotech companies, collaborating with in-house and outsourced partners. She successfully developed the clinical operations department and launched the first clinical trials in cell therapy for a French start-up from 2001-2005, which is now a larger biotech company. From 2007-2012 she worked as a clinical trial manager for Merck Serono/Switzerland where she managed worldwide clinical trial-level activities ensuring alignment of guidelines, budget, timelines and quality, and consistency across clinical documents. She has also done some consulting work for a large US pharmaceutical company where she supported the clinical team in managing the bio-samples and in collecting and organizing the clinical program documentation. Recognized as a strong, dependable, and energetic team player, she is seeking part-time project management responsibilities in a supporting or administrative role, where she can combine her science background and her administrative and operations experience. She is proficient in MS Office and Google suite and is fluent in French. She has an MS in Sciences from Paris University-France.

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