Duties WHAT IS THE COMMUNICATIONS AND LIAISON (C&L) DIVISION? A description of the business units can be found at Vacancies will be filled in the following specialty areas Office of Communications, Planning and Content Development Branch and Employee Communications Branch. The following are the duties of this position at the full working level. Recommends policies, progra

At Alcon, we are driven by the meaningful work we do to help people see brilliantly. We innovate boldly, champion progress, and act with speed as the global leader in eye care. Here, you'll be recognized for your commitment and contributions and see your career like never before. Together, we go above and beyond to make an impact in the lives of our patients and customers

Pushing the frontier of solid cancer therapy, Neogene Therapeutics is a global, clinical stage biotechnology company built on the premise of innovation and novel paradigm changing science. Using tumor mutation profiles to engineer fully individualized T cell therapies, Neogene is bringing new hope to address the current limitations of treatments available today. We offer

Recruiter Spencer Gregory Hale Regulatory Affairs Specialist II Neuromodulation About the role Support the regulatory submission activities to obtain and maintain approvals for conducting clinical investigations and for commercially distributing products worldwide. Participate in activities to ensure compliance with worldwide regulatory requirements. Your responsibilities

Government Relations Manager United States Virtual Req #463 Thursday, December 28, 2023 Want to help people learn the newest ways of working and getting things done? How you'll make a difference You will be responsible for planning, developing and executing a strong positive government relations and advocacy program for PMI. You will be fostering a community relationship

Advantage Technical is seeking a Regulatory Affairs Specialist for our client in Irvine, CA. This position is Hybrid Monday Wednesday Friday on site and Tuesday Thursday remote. Support the EU's In Vitro Diagnostic Regulation (IVDR) transition activities that will impact all our client's products currently CE Marked under the IVD Directive. Activities include preparation

The UCLA CORE Kidney Health Program is seeking an experienced RegulatoryProject Manager to oversee all regulatory aspects of clinical trials, clinical programs,our patient and community outreach program, education and training, and assistwith administrative tasks. You will be responsible for the oversight ofregulatory coordination for clinical research studies. This inclu