single-vacancy Project lead / (senior) manager - Iperion Project lead / senior consultant Regulatory Information Management

Project lead / (senior) manager

As a Project lead / (senior) manager within the area of Regulatory Information Management, you will be responsible for the delivery of our projects to the clients. Typical projects involve data standards assessments and implementation, regulatory information management system selection and implementation, RA business process optimization, defining information management strategy and roadmaps. You will lead a team of multiple consultants and subject matter experts, all with the common goal to deliver sustainable advice and results to the client.

Iperion – a Deloitte business is a young and ambitious team with the mission to increase digitalization and transparency in Life Sciences industry. We aim for sustainable changes within organizations by process improvements, data interoperability and implementation of technology and data standards in the regulatory landscape. Our work field includes both industry as well as regulators. Our mission drives us to deliver value to our international customers and requires motivated and passionate consultants.

Are you keen on becoming part of a group who shares the joint drive to make a difference? Then, join Team Iperion!

Your responsibilities

  • Ensuring high quality delivery of projects to clients, including project & change management and coordination activities.
  • Developing a deep understanding and knowledge of Iperion product areas and applying them to relevant projects (externally and internally).
  • Establishing an excellent working relationship with the client.
  • Identification of new business opportunities.
  • Defining various approaches and methodologies for business opportunities.


What you offer

  • You have completed MSc or at least BSc in the area of life sciences (e.g. Biomedical Sciences, Medical Biology) or have relevant alternative education (e.g. Computer Science or Technical Business Administration) with interest in Life Sciences.
  • You have 4+ years of experience in (regulatory) information management or in other pharmaceutical/regulatory domains, such as data standards, IT systems, business processes, and project management.
  • You have proven ability to successfully deliver value to the clients.
  • You have strong communication skills and the ability to build effective working relationships with both colleagues and clients.
  • You are not afraid of new challenges and have a flexible and constructive attitude / work ethic.
  • You are proficient in English (written and verbal communication).
  • You are willing to travel internationally.
  • You are a team player, with (developing) leadership skills.
  • You are motivated, pro-active and reliable.

What we offer

  • A diversity of interesting and challenging projects with different clients.
  • The opportunity to work within a dynamic and growing organization
  • Working in an international setting within a global organization, with the intimacy of a small team, where communication lines are short.
  • A welcoming down-to-earth environment, with like-minded individuals and team events.
  • A 32-40 hours working week with a competitive salary, based on your experience.
  • Great opportunities to pursue your ambitions, which include a personal development plan supporting your professional and personal growth.

If this role as project lead / senior consultant Regulatory Information Management is appealing to you, then we’d love to hear from you!
Please send your motivation including what you would bring to the company and why along with your CV to

If you have further questions about this vacancy, please reach out to our HR officer Tamara van Lieverlooy via 06-55 55 16 24 or fill in the form below.

Besides Project Leads, we are also recruiting Senior Consultants Regulatory Information Management, Medior Consultants and Junior Consultants.

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