Okay, let’s tackle this. So Mary has a strong background in regulatory affairs, with skills in pharmaceutical industry, licensing, and corporate law. She’s working in Greater Boston, which is a hub for biotechnology and pharmaceutical companies. Her experience in regulatory submissions, clinical trials, and regulatory requirements is valuable. Considering her skills and location, I’m estimating her hourly rate to be around $125, which is in line with industry averages for regulatory affairs professionals in the lifesciences sector. This rate is slightly lower than what top-level executives or those with more senior roles might charge, but it reflects her mid-level expertise and location.