$90K - 130K a year
Lead and drive multiple regulatory pharmaceutical manufacturing projects through all phases, managing risks, dependencies, and deliverables while collaborating with internal and external stakeholders.
At least 5 years of project management experience in pharmaceutical manufacturing regulatory projects, understanding of drug development lifecycle, strong organizational and communication skills, US-based with East Coast hours availability.
Our client is seeking a Remote Consulting Regulatory (Pharmaceutical Manufacturing) Project Manager for 6+ months. The Regulatory Project Manager will work with the PMO, other Project Managers, project teams, and the business to develop project artifacts and drive project execution and delivery for one or more concurrent projects. The Project Manager will set up and lead work shops; ask detailed drill down questions to understand true risks, dependencies, options, and "what ifs"; track deliverables and interdependencies, report on project status; and drive the project through phases and to successful completion. To be considered, you must have: • At least 5 years of Project Management experience in Pharmaceutical Manufacturing and related Regulatory concerns • A good understanding of the Drug Development process and lifecycle, including but not limited to: Clinical Trials, CMC, Labelling, and Policy and working with Health Authorities • Proven experience driving projects to completion • Proven ability to collaborate across an organization as well as with both internal and external parties • An orientation to ask detailed drill down questions in a non confrontational manner • Solid organizational skills and an ability to prioritize and execute effectively • Strong verbal and written communication and interpersonal skills • Must be US based and willing / able to work East Coast hours • May be occasional travel to the Northeast
This job posting was last updated on 10/7/2025