Can please someone help me to revise this paragraph? Ty!

I would like to know in detail about preclinical/regulatory protocols and seems that no one here in Yongin site can provide me proper lessons and would like to ask you, if possible, I can shadow someone from the HQ to attend meetings where I can observe and learn. I am reading thru the FDA site about IND protocols but it seems I need a real-life experience to fit in what I have learned from the FDA site.