Mieke Tempels

Expert – Clinical Research Professional

  • Regulatory & ethics expert
  • Clinical Project Management
  • Clinical Data Management
  • Quality Management



Who is Mieke

I am an engaged person, eager to take initiatives and responsibility to move things to the next level. My interest in science and research and my will to make a difference in medical treatments and healthcare, brought me to my role as a Clinical Research Professional. I developed my skills and gained experience working for a big Pharma CRO.

After many interesting projects, I chose to switch from pharma to medical devices. This enabled me to use my experience to manage projects efficiently for a company close to my hometown and with an amazing team. I love motivating people, networking, traveling, and giving advice and training to bring out the best in people. Currently responsible as Team Lead as well as Quality Management.


Expertise and background

After my studies in Biomedical and Pharmaceutical Sciences, I have gained a broad experience in organizing and managing multiple international clinical trials in various therapeutic areas while working for a multinational CRO. I have networked with many people and worked in teams with different backgrounds. Currently, working for a medical device CRO gave me the opportunity to become an expert in clinical project management, regulatory as well as quality management.



I like sharing knowledge in a clear way, with examples and cases. A lot can be learned by listening to issues and searching for solutions together. I think providing training is most efficient when it is interactive.