Overview A World Leading Pharmaceutical Company located in CT is hiring a Project Office Specialist with 3-5 years industry experience. If you have clinical supply chain management experience, please apply! Responsibilities
As a Project Office Specialist, you will closely collaborate with the Head of the Project Office to set-up and continuously develop the new Global Clinical Trial Services Unit Project Office.
With your experience in supply chain management, you contribute to maintain and improve the global project plan templates in Planisware and act as CTSU Key-user role to ensure correct project plans for all NBE, NCE and NTM trials including IIS and client sponsored trials for commercial products.
Thanks to your expertise in clinical supply chain management, you are responsible to generate and provide reports from several systems to support global CTSU management and medical budgeting.
With your knowledge in GMP you contribute to daily operations to support project work, trial management and supply chain activities for Clinical trials supplied by CTSU.
Requirements
Bachelors' Degree
3-5 years working in Pharma Industry
Ability to learn multiple computer systems.
SAP software-based computer systems experience.
MS Office and MS Teams experience
GMP and GCP Pharmaceutical Industry Regulations knowledge
BenefitsSystem One offers eligible employees health and welfare benefits coverage options, including medical, dental, vision, spending accounts, life insurance, voluntary plans, and participation in a 401(k) plan.