Life Sciences & Technology
| Clinical Research & Clinical Affairs
A BDN client in Texas is looking for a regulatory affairs specialist who can provide six months of consulting coverage. Our client is looking to hire a senior level consultant to help assist with multiple types of regulatory submissions for class I - III medical devices. The types of submissions include TMF, US dossiers, EU dossiers, and 510ks. This is a hands-on position where the consultant will be responsible for the day-to-day execution of the tasks. Candidates for this position should have at least five years of submissions experience, preferably with an orthopedic background.