The Senior Associate will play a key role in supporting regulatory and human factors engineering initiatives. Responsibilities include drafting usability engineering files, conducting use related risk analysis, post-market surveillance data analysis, designing usability studies, and drafting reports.
This fellowship program invites applications from professionals with advanced degrees and strong backgrounds in science, health policy, and/or law, offering a perspective into regulatory science/policy, drug development, and market access. The fellow will gain knowledge of regulatory issues facing healthcare companies by researching, presenting, and publishing insights on regulatory topics.