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.
Job details are sourced from the employer's original posting.
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