Duties/responsibilities:
路Will be working on procedural documents via Mastercontrol system and Viva
路Will be working on harmonizing effort- someone who will oversee the harmonization process
路A good Project Manager
路Will be starting the QMS
路Ability to work cross-functional and cross-developmental, someone who can work really well with vendors and clients
Qualifications:
路Knowledge of
路Knowledge of LMS
路Strong Project Management skills
路Pharmaceutical experience- must have
路Background in Clinical trial work and R&D
路Global harmonization process experience- nice to have
路Someone who has experience with SOP- must have
路Previous SOP harmonization experience- nice to have
路 Not looking for someone who has manufacturing background
路PMP certification is not required
Integrated Resources INC
https://careers.smartrecruiters.com/IntegratedResourcesINC