Project Manager

Mandatory Skills: Pharma IT, GxP Project, PMP Certification Domain Experience • Working knowledge of ICH Guidelines and GCP including international regulatory requirements for the conduct of clinical development programs. • Broad knowledge of drug development process and client needs • Prior experience working on regulatory submissions • Familiar with 21 CFR part 11, GXP and other Life Sciences regulations Technical Experience • Experience with LIQUENT Insight publisher, Veeva platform strongly preferred; however, consideration will be giving to candidates with experience with other electronic publishing systems • Experience with Waterfall and Agile development • Thorough understanding of Software Development Life Cycle (SDLC) and all related documentation All your information will be kept confidential according to EEO guidelines.