single-vacancy (Senior) Manager Regulatory Information Management - Iperion

(Senior) Manager Regulatory Information Management

Iperion – a Deloitte business is looking for a (Senior) Manager Regulatory Information Management (RIM) to join our growing international team.

As a (Senior) Manager, you will be responsible for 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 roadmap. You will lead a team of other consultants and subject matter experts, with a common goal to deliver sustainable advice and results to the client.

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.

Your responsibilities

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

Personal blogs

Current team members have shared their experiences in their personal blogs. Read how Nadia experiences her role as project lead, how Amy started in her job as director and how Camiel has grown to an experienced SME.

What you offer

  • You have completed MSc or at least 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 interest in Life Sciences
  • You have 4+ years of experience in (regulatory) information management, or other pharmaceutical/regulatory domain, such as data standards, IT systems, business processes, and project management
  • You are proficient in English (written and verbal communication)
  • You are willing to travel internationally
  • You have proven ability to successfully deliver value to the clients
  • You have great communication skills and ability to build effective working relationships internally and at clients
  • You are a team player, with leadership skills
  • 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 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 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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