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Monitor progress and conduct of their respective projects, including all data cleaning and QC activities to ensure all remain on target to project timelines. Be responsible for participating in ongoing data review throughout the conduct of the study, including being responsible for the correction of
August 15, 2026 by Nexcella, Inc.Quebec, ca
Monitor progress and conduct of their respective projects, including all data cleaning and QC activities to ensure all remain on target to project timelines. Be responsible for participating in ongoing data review throughout the conduct of the study, including being responsible for the correction of
August 14, 2026 by Nexcella, Inc.Longueuil, Quebec, ca
Associate Director of Regulatory Affairs.The Director of Regulatory Affairs will support the regulatory strategy and execution for clinical trials conducted under FDA/EMA/Other Regulatory agencies regulations.This role is responsible for preparing, submitting, and maintaining regulatory documents an
August 14, 2026 by Nexcella, Inc.Laval, Quebec, ca
Associate Director of Regulatory Affairs.The Director of Regulatory Affairs will support the regulatory strategy and execution for clinical trials conducted under FDA/EMA/Other Regulatory agencies regulations.This role is responsible for preparing, submitting, and maintaining regulatory documents an
August 14, 2026 by Nexcella, Inc.Longueuil, Quebec, ca
Monitor progress and conduct of their respective projects, including all data cleaning and QC activities to ensure all remain on target to project timelines. Be responsible for participating in ongoing data review throughout the conduct of the study, including being responsible for the correction of
August 14, 2026 by Nexcella, Inc.Montreal, Quebec, ca
Monitor progress and conduct of their respective projects, including all data cleaning and QC activities to ensure all remain on target to project timelines. Be responsible for participating in ongoing data review throughout the conduct of the study, including being responsible for the correction of
August 14, 2026 by Nexcella, Inc.Longueuil, Quebec, ca
Be responsible for handling of non-CRF data, including lab data and image handling. Monitor progress and conduct of their respective projects, including all data cleaning and QC activities to ensure all remain on target to project timelines. Be responsible for participating in ongoing data review th
August 14, 2026 by Nexcella, Inc.Laval, Quebec, ca
Associate Director of Regulatory Affairs.The Director of Regulatory Affairs will support the regulatory strategy and execution for clinical trials conducted under FDA/EMA/Other Regulatory agencies regulations.This role is responsible for preparing, submitting, and maintaining regulatory documents an
August 14, 2026 by Nexcella, Inc.Laval, Quebec, ca
Be responsible for participating in ongoing data review throughout the conduct of the study, including being responsible for the correction of errors and discrepancies management for the life of a project. Be responsible for handling of non-CRF data, including lab data and image handling. Monitor pr
August 14, 2026 by Nexcella, Inc.Laval, Quebec, ca
Associate Director of Regulatory Affairs.The Director of Regulatory Affairs will support the regulatory strategy and execution for clinical trials conducted under FDA/EMA/Other Regulatory agencies regulations.This role is responsible for preparing, submitting, and maintaining regulatory documents an
August 08, 2026 by Nexcella, Inc.Quebec, ca