About

I came to health research through a national parcel network.

  1. 2015TehranMBA, quality engineering
  2. 2016TehranMSc, socio-economic systems
  3. 2017Iran PostWhere the parcel hubs should go
  4. 2019Leuven and HasseltDual PhD
  5. 2024Leuven and HasseltPostdoctoral researcher
  6. 2026Innovation MandateWith Johnson & Johnson Innovative Medicine
Leuven and Hasselt2019 to nowTehran2015 to 2019
Cities where I have given talks. From Tehran to Leuven4,056 km and Hasselt4,012 km, as the crow flies. Map data: Natural Earth.
On this page
  1. Into health
  2. The USB stick
  3. In the middle
  4. Teaching
  5. Where I am going
  6. Outside work

From systems engineering into health

I trained in Tehran, first an MBA in quality engineering and then an MSc in industrial engineering on socio-economic systems, so my picture of engineering came from logistics and industrial systems. From 2017 to 2019 I worked on Iran Post's parcel network, on a question that sounds simple: where should a national post put its sorting hubs? I built a simulation of the whole network and let a search run over it for a better layout. The best one came out 15% lower on projected transport cost, in the simulation, and it ended up as a decision support dashboard for the executives who had to choose. What I liked most was that last part: turning the analysis into something the people making the decision could actually use. I carried that preference with me into health research.

Cities, and where their parcels are sortedold hubbetter position
A sketch of the problem. In the real simulation, the best layout cut projected transport cost by 15%.

In 2019 I started a dual PhD in Belgium, in electrical engineering at KU Leuven and in biomedical sciences at Hasselt University. That meant a new country and a new field at the same time.

The USB stick

When I started, I imagined someone would hand me a dataset on a USB stick, and I would take it away and find something in it.

Instead, before I could choose any method, I had to find out what clinicians actually wanted to know, what the records could answer, and what the people responsible for those records would allow. It was almost two years before I worked with real world data. That was much slower, and much harder, than I expected.

What I expectedWhat it wasContents: 0 bytes. I checked.a dataset, handed overpeople, questions, permissions
A sketch: the USB stick I expected, and the people I needed instead.

In the middle

For a while my work sat between two groups, and neither was quite sure what to make of it. Some engineers told me it was not technical enough, and some clinicians and epidemiologists told me the opposite: too technical, and not methodological enough. I heard both.

On one study I might need a clinician, an engineer, a registry holder and a lawyer to agree, and each of them starts from a different question. A lot of my work is finding out what each one needs before they can say yes, and I have done that with registries and consortia in more than thirty countries.

hold the datatreat the patientsdecide what is allowedin the middle
The people around one study, and me in the middle.

Teaching

Ashkan Pirmani speaking at a white lectern with a laptop open in front of him
                      and a headset microphone on.

I taught in the Data Science in Healthcare course at Hasselt University for two academic years, and I have supervised seven master's theses in artificial intelligence at KU Leuven.

Where I am going

In 2026 I won a personal grant from the Flemish government, an Innovation Mandate, which is meant to carry research out of the university and into a company. It goes to one researcher and one company together, and mine is with Johnson & Johnson Innovative Medicine. I wrote the proposal and defended it.

The goal is drug safety: comparing people who take one medicine with people who take another, on health records and insurance claims, in my case Optum's. When each site has only a few patients, that comparison is hard to keep fair. The mandate started in September 2026, with the methods first; drug safety comes in its second year. The question I am working on now grows out of my disability progression study: models that stay reliable when each site has few patients and the sites differ. Under all of it is one question: how much each site should learn together with the others, and how much on its own.

I don't know yet whether these methods hold up on claims data, outside multiple sclerosis. More on the mandate.

Outside work

Azeri is my mother tongue. I went to school in Persian, and learned Turkish and the Azerbaijani of Azerbaijan on the side. English came after that, and I am still working on Dutch.

Azeri, my mother tongueتورکیmother tonguePersian, the language of schoolفارسیschoolTürkçeAzerbaijani, as written in AzerbaijanAzərbaycancaon the sideEnglishnextIk ben nog aan het oefenen.Nederlandsstill coming
Each language written in itself.

I watch Formula 1 . If you ask me Verstappen or Hamilton, I will say Alonso and Räikkönen

Let's talk.

If your question depends on real world health data, I probably want to hear about it.

Email me

TurkishMerhabaAzeri, my mother tongue, as written in Urmia: xoş gəldin, welcomeخوش گلدینAzerbaijani, as written in AzerbaijanSalamPersian, the language of school: dorudدرودEnglishHelloDutch, as said in FlandersDagyou
A greeting in each language I speak, where it lives.