Job Description
The Senior Associate will play a key role in supporting regulatory and human factors engineering initiatives across a diverse portfolio of medical device and life sciences clients. Responsibilities include: Drafting usability engineering file, conduct use related risk analysis, conduct post-market surveillance data analysis, design usability studies and draft protocols. Support usability study execution and report drafting. Develop and execute regulatory services for client companies, including Regulatory Submissions, Regulatory Strategy, Analysis & Development Design, Review & Implement Pre-Clinical Testing. Communicate with regulatory bodies and clients with support of senior MCRA staff and work collaboratively with other MCRA departments.
About MCRA
MCRA, an IQVIA business, is a leading medical device advisory firm and clinical research organization (CRO).