I feel there's a paradigm difference here. Classical scientific method says "make hypotheses, test, confirm or infirm". That was the golden standard for 400 years. It works very well, but it has weaknesses (what doesn't). First is that it doesn't specify how you should select the hypotheses on which you want to perform (costly) experiments, and the second is that it's very bad at processing partial data. You can confirm on infirm - with some complicated math on how good the experiment was.
Nowadays we have much better protocols, mostly based on the Bayesian method which is much more robust on getting small pieces of information. One of its principles is actually this: no matter how small and useless an experimental result is, it should still budge your understanding of the phenomenon even if it's a tiny bit. There are some caveats here as well, but overall it's a whole different ballgame from the big, old, clunky scientific method.
So how does this apply to this situation? You have a cycle of 2 weeks for covid infections. A completely-pulled-out-of-my-ass protocol would involve 100 very-low-risk individuals split into vaccinated and control and infected deliberately with various doses. You get some data from this: how well is the vaccine working? how is the disease progressing depending on initial viral dose?
For the next 2 weeks you switch to slightly higher vulnerable populations, again split into control/vaccine.
For the next 2 weeks you ditch the control to lower the risk, and add another decade to the age of the population.
Now you have good enough data to start vaccinating vulnerable population at large.
You keep testing on volunteers, because you're about to vaccinate millions and you NEED extra data, like what's the fastest protocol to vaccinate everybody. Except now you have enough efficacy data to know that you won't kill your vaccinated volunteers, so you start using more mixed populations with higher ages - though the bulk will still be low-risk. And play with whatever variables you need adjusting, like vaccine dosage or booster timing, and adjust the population-at-large protocols based on that.
Compare this with what we did, which is literally last century methodology. We pulled out of the ass a protocol: vaccine dose of X, booster timing of 3 weeks. Then we tested it in a large scale long term trial. We confirmed it worked. And used it as-is, and declared that any change will require another large-scale long-term trial. Look at the definition of the scientific method in the beginning of my comment. It's just not common sense in a pandemic, except for bureaucrats minimizing their personal risk. Which is why my rather justified anger with the system.