To answer your question, I find with most recrystallization processes (unless your going for faceted stones), follow a similar motif. Start with your poor solvent, the less solvent the better, heat it to fully dissolve, let temperature drop naturally with agitation. This can take hours or days. Once it looks like no more crystal growth is occurring you can either decant your mother liquor and end it, or chill it further if there is more remaining. That’s a good blanket way to develop a method.
So what this looks like is dissolve at high heat, let cool on bench, stir plate or ultrasonic bath; this is where the solution will get cloudy because it is seeding. Bring outside to get to 0C and let it go until no more growth happens. Place in freezer to crystallize further.
You can always get fancy with it; temperature pulsing, solvent blends, louching, solvent removal, but start simple and add steps as needed. This should yield some nice looking chunks while not taking too long. Really the slower you go, the better your recrystallization will be (purity-wise)
) and looking at doing something like this.