single-vacancy Medior Consultant Regulatory Information Management - Iperion

Medior Consultant Regulatory Information Management

Iperion – a Deloitte business is a young and ambitious team with a mission to increase digitalization and transparency in Life Sciences industry. We aim to make sustainable changes to the 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 attracted to the idea of becoming a part of a group that shares the drive to make a difference? Then joining Team Iperion is your next step.

We are looking for a Medior Consultant in Regulatory Information Management area to join our growing team.

As a Medior Consultant, you will participate in ongoing projects at our clients. You will be a part of a project team, led by a project lead and responsible for performing activities and producing deliverables according to the project plan. Some examples of projects: RA business process optimization, IDMP assessment, definition of information management strategy. Your activities will range from business process mappings, data analysis, preparation of reports and documents, participation in workshops, support in system implementation.

Your responsibilities

  • Execution of activities and deliverables according to the project plan, e.g. data analysis, process mapping, support in workshops, preparation of reports
  • Establishing a good working relationship with the client
  • Developing a good understanding and knowledge of Iperion product areas and supporting projects as content expert
  • Supporting Senior Consultants in preparation of approach and methodology of new business opportunities and in minor project management activities
  • Pro-actively addressing own professional and personal growth

What you offer

  • You have completed BSc in area of life sciences (e.g. Biomedical Sciences, Medical Biology) or have relevant alternative education (e.g. Computer Science or Technical Business Administration) with special interest in Life Sciences
  • You have 2+ years of experience in pharmaceutical/regulatory domain, such as (regulatory) information management, data standards, IT systems, business processes, and/or project management
  • You are proficient in English (written and verbal communication)
  • You are willing to travel internationally
  • You have great communication skills and ability to build effective working relationships internally and at clients
  • You are a team player
  • You are motivated, pro-active and reliable
  • You are not afraid of new challenges and have a flexible and constructive attitude

What we offer

  • A diversity of interesting and challenging projects with different clients
  • Opportunity to contribute to our growing and dynamic organization
  • Working in an international setting and 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 (e.g. Friday drinks, company outings, sports events)
  • A 32 to 40 hour working week with a competitive salary, based on your experience
  • Great opportunities to work on your ambitions including a personal development plan which supports your professional and personal growth

If this role 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 at 06-55 55 16 24.

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