Hobson Prior is seeking a Technical Documentation Specialist to join a dedicated team. This role will focus on creating and managing important documents related to medical devices, ensuring they meet European standards. The successful candidates expertise ...
... IRB and, where appropriate to Regulatory Authorities Ø Interfaces with Investigators, external ...
... supervision while adhering to compliance regulatory policies. You are capable of ...
... including ICH GCP and local regulatory requirements. Solid communication and computer ...
... division. We work closely with regulatory authorities and payers to find ...
... Affairs, Clinical Sciences, Operations, and Regulatory, and provide guidance to Commercial ...
... . Ensure all activities comply with regulatory and legal standards. Act as ...
... approval, as well as preparing regulatory submissions Balancing sponsor generated queries ...
... supervision while adhering to compliance regulatory policies. You are capable of ...
... IRB and, where appropriate to Regulatory Authorities Ø Interfaces with Investigators, external ...