I think Chris yesterday (as an expert in the field) said that he was extremely confident that no safety shortcuts would have been taken, that it’s mainly administrative savings that have been found in the timeframe (as well as some differences in opinions about efficacy). This seems to also be the conclusion of almost all experts.
All of the data will need to go through expert regulators before they are ever approved for human use. If there are any safety concerns whatsoever remaining (which is extremely unlikely) then they will be picked up at that stage.
Each to their own Doe, and you’ve gotta do whatever makes you most comfortable, but you’d hate to have a situation where you chose not to get the vaccine because of some concerns that were ill-founded and then you ended up getting sick.