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Principal Project Manager

Job in Maryland Heights, St. Louis city, Missouri, 63043, USA
Listing for: Curium Pharma
Full Time position
Listed on 2026-07-08
Job specializations:
  • Management
    Operations Manager, Program / Project Manager, Change Management
Salary/Wage Range or Industry Benchmark: 100000 - 130000 USD Yearly USD 100000.00 130000.00 YEAR
Job Description & How to Apply Below
Location: Maryland Heights

Principal Project Manager

Date:
Jun 18, 2026

Location:

St. Louis, MO, United States, 63146

About Curium

Curium is the world's largest nuclear medicine company with more than a century of industry experience. We develop, manufacture and distribute world‑class radiopharmaceutical products to help patients around the globe. Our proven heritage combined with a pioneering approach are the hallmarks to deliver innovation, excellence and unparalleled service. With manufacturing facilities across Europe and the United States, Curium delivers SPECT, PET and therapeutic radiopharmaceutical solutions for life‑threatening diseases to over 14 million patients annually.

The name ‘Curium’ honors the legacy of pioneering radioactive researchers Marie and Pierre Curie, after whom the radioactive element curium was named and emphasizes our focus on nuclear medicine. The tagline ‘Life Forward’ represents our commitment to securing a brighter future for all those we serve: an enhanced quality of care for our patients, a trusted partner to our customers, and a supportive employer to our valued team.

Summary

of Position

This Principal Project Manager role provides a unique opportunity to collaborate across the different functions including Regulatory Affairs, Research and Development (R&D), Operations, Quality, Supply Chain, Finance, Legal, HR, Engineering, Marketing and Commercial. This individual will work closely with the Vice President – North American Project Management Office and the Senior Director Project Manager – North American Project Management Office to implement Curium's strategic initiatives and projects.

This position requires effective communication on program status to senior leadership across the company.

Work Schedule: Monday – Friday 8:00 am – 5:00 pm. Hours could be adjusted.

Essential Functions
  • Maintain operational compliance with US and international regulatory agencies and guidelines (e.g., FDA, EU, HC, TGA, PIC/S, ISO, USP, NRC, cGMP, etc.).
  • Coordinate and align multiple shared services activities between board‑approved New Product Development (NPD) and MOB‑related initiatives.
  • Provide Project Management Services for North America Strategic Business Initiative projects that are classified as NPD or MOB.
  • Facilitate key meetings, including core and designated sub‑team meetings.
  • Coordinate MOB and Strategic Business Initiatives to be integrated in escalation and governance processes where critical projects are managed and reported.
  • Support efforts to improve and enhance the PMO process/governance structure and systems initiatives, including resource management across all functional groups for NPD, MOB and other Strategic Business issues; optimize the financial forecasting process; support PMO portfolio software implementations; assist with execution of stage‑gate process for all projects.
  • Provide PM Services, when necessary, to ensure business continuity within the PMO.
  • Present project status, issues and risks to the Project Review Committee team members and provide recommendations on project direction.
  • Work with the PMO group during the concept phase to provide scoping, scheduling and cost information for requirements.
  • Provide PM services/support for elements of Integration activities for M&A.
  • Use Project Management systems to capture and share information from each project to drive continuous improvement and best practices.
  • All other responsibilities as assigned, with or without accommodation.
Requirements
  • Bachelor’s level degree in engineering or related sciences or equivalent experience.
  • 8 or more years of experience in the pharmaceutical industry and leading cross‑functional projects.
  • Technical understanding of pharmaceutical processing.
  • Knowledge/experience in aseptic/terminally sterile operations; isolator technology a plus.
  • Knowledge/experience in radiopharmaceutical industry and operations a plus.
  • Experience in manufacturing operations preferred.
  • Team member and team leader experience.
  • Strong evidence and mastery of being a team contributor.
  • Demonstrates strong interpersonal skills, including the ability to maintain composure and professionalism under pressure.
  • Allocate resources effectively across multiple…
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