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