Responsible for project activities associated with monitoring functions of phase I through phase IV clinical research studies and Real World Evidence (RWE) studies, while continuing to develop knowledge of drug development process, International Council for Harmonisation
Job Purpose/ Summary: Independently manage essential regulatory documentation (as applicable) for submission to country/regional/site Institutional Review Boards (IRB), Ethics Committees (EC), Competent Authorities (CA) and/or other Regulatory Bodies for all clinical studies performed globally. Interact with, assist,
Executive Assistant Department: Operations Employment Type: Permanent Location: Covington, Louisiana Reporting To: President, US & Global Expansion Compensation: $55,000 - $70,000 / year Description At Veriforce, we help companies in high-risk industries keep their people, worksites,