About this role
Consultant 1 at ELIQUENT Life Sciences. Location: Columbus, Ohio, United States. Role: writing documentation, executing protocols, conducting investigations Requirements: Early-career consultant to write technical documentation, execute qualification/validation protocols, perform investigations, and support clients; proficient in Microsoft Office and familiar with FDA/cGMP documentation practices; bachelor’s degree preferred. Category: Business Development Seniority: Entry Level Tools: Microsoft Word, Microsoft Excel, Microsoft PowerPoint Commitment: Full Time Workplace: Field Languages: English