Loading...
Share this Job
Apply now »

 

Let's push the boundaries together and make the most of your talents!

Global Submission Project Manager

Location: 

Anderlecht, Brussels, Belgium

Job Function:  Regulatory Affairs
Job ID:  67913

.

To strengthen our Global Regulatory Affairs Department based in our Headquarters in Brussels, Belgium we are looking to fill the position of: Global Submission Project Manager.


As a Global Submission Project Manager, you will be focused on the delivery of a project or set of responsibilities that will further the value creation for patients.

 

This is typically captured via the five stages of a project: setting the goal with the sponsor, defining the project strategy, planning the project, executing against the plan and closing out through lessons learned and measuring the impact.

 

The Submission Project Manager skill set requires using standard project management tools such as a project charter, scope of work, budget, resources as well as scenario planning, risk/opportunity assessment, trade-off analyses, and partnering with stakeholders to appropriately prioritize and execute the project. These deliverables contribute to the company’s success and depending on the project, may take a long-term view.

 

Additionally, the Submission Project Manager requires working knowledge of the Common Technical Document, Drug Development and Regulatory Filing procedures.

 

Operationally, you will be focused on driving the submission team in alignment with the Project plan, including meeting outcomes/actions, budget preparation (where applicable), challenging of resource estimates and utilization, and on adherence to agreed timelines.

 

You will act as champion for Project Management techniques and processes, coaches team members in these areas and shares lessons learned for continuous improvement.

 

Interested? For this position you’ll need the following education, experience and skills:

  • Previous pharmaceuitcal or CRO experience is a must. 
  • A Degree in relevant field or equivalent. 
  • Prior experience from either a cross functional role or from a line function.
  • Has worked in a global environment with matrix structure and/or project organization with strong project management experience, in the pharmaceutical industry, CRO or comparable partner organization for drug development.

 

Why you should apply

At UCB, we strive to attract passionate and outstanding talents who thrive on change and are ready to bring real value to patients. Working for us you’ll discover a place where you can grow and express your full potential. We place an emphasis on innovation, collaboration and impact. Through meaningful recognition and a motivating work atmosphere, we aim to provide an optimal experience by caring about and valuing our employees – just as we do for the patients we serve.

 

If you believe you are the perfect match to join us on our pioneering adventure, then we invite you to apply and tell us more about your profile and motivation.

.

Apply now »