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Marc Abernathy

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Marc Abernathy
Gegend:
Cologne, Germany
Arbeit:
Regulatory Affairs Specialist
Organisationen:
Member, American Medical Writer's Association
Hochschulen:
 University of California, Berkeley (History, B.A.), University of Cambridge/Berlin School of English (English Teacher Training, CELTA - Certificate in English Language Teaching to Adults)
Status:
Employee
Sprachen:
English
Ich suche:
writing and editing project work, English training, telecommuting, IRB and regulatory consulting work
Ich biete:
regulatory affairs, FDA regulations, DHHS regulations, ICH guidelines, GCP guidelines, IRB (ethics board) review process, HIPAA, consent form writing and editing, managing, medical writing, medical editing, technical editing, protocol review and editing, proofreading, copy editing, writing press release and marketing material
Interessen:
telecommuting, project work, skiing, bicycling, travel, languages, museums
Über mich:
I have nearly six years of regulatory and consent form editing experience. My experience in IRB (ethics board) review uniquely positions me to assist small and medium-sized biotechnology and pharmaceutical firms understand the review and approval process at U.S. IRBs. In particular, I can provide protocol and consent form appraisal and editing and regulatory interpretation that can assist firms ...

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Marc Abernathy
Gegend:
Kln und Umgebung, Deutschland
Zusammenfassung:
Clinical Trial Regulatory Experience, Editing, and English Training
Berufserfahrung:
Quorum Review IRB (Research Ethics Board) (In Privatbesitz; Branche: Pharmazie): Senior Regulatory Analyst,  (Januar 2008-Mrz 2010) Appointed to newly-created position to conduct regulatory project work. Researched and drafted memoranda and white papers for IRB policy positions a...
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