Clinical Supply Project Manager (Hybrid)

Kardium • Burnaby, British Columbia, Canada • 22h ago

Your opportunity

Meaningful work you will be a part of Your Responsibilities Will Include

Own and train new users in theInvestigational Product Management Process.
Manage continuous improvement of the current process.
Maintain and ensure accurate Investigational Product records.
Ensure escalation of issues related to the timeliness and quality of Investigational Product delivery to key stakeholders in a timely manner.
Maintain awareness of key trial related metrics (i.e. study start-up and activation details) to support in-time study support for items related to site start-up requirements.
Coordinate with internal teams to ensure correct equipment availability for clinical trials.
Communicate equipment status, risks, and issues to stakeholders.
Manage the equipment configurations, and ensure compliance with company policies, procedures, and applicable industry regulations.
Support development of other process related documentation for Investigational product management
Support the operations team in other duties as assigned.

What You Bring To The Team

Bachelor's degree in engineering or a relevant Life Sciences field
2 years of experience managing projects.
5 years of experience working in engineering or life sciences.
Experience in Microsoft Office Suite (Excel, Word, PowerPoint, Outlook, Teams).
Proficiency with project management tools such as Microsoft Project and Smartsheet.
Knowledge of Clinical Operational practices and workflows is an asset.
Experience working with Medical Devices or other regulated industry is a plus.
Strong organizational, time management, communication, and problem-solving skills.
Excellent verbal and written communication skills.
Ability to work in a fast-paced environment and manage multiple priorities.

Compensation