I agree with a lot of the post above in regards to the amount of paperwork that potentially needs to be done within this field. I don’t have experience in working within Clinical Trials, however, as I have found just by reading and discussing with other colleagues, it seems that the biggest con is the actual execution of the protocol and study and less of the paper work. I have heard that some protocols are difficult to understand and trying to analyze and find significant data is almost like looking for a needle in a haystack. Therefore, I know personally I would not want to be involved in this line of work.