... are looking for a Senior Regulatory Affairs Manager Consultant with 10+ years of experience in regulatory affairs, including CMC expertise. This challenging ... : 10+ years of experience in regulatory affairs Extensive knowledge of CMC writing ...
... currently looking for a Senior Regulatory Affairs Consultant (Project Lead) As a ... are functioning Work with RAL Regulatory Affairs Lead and or TL Technical ... to have Extensive years of Regulatory Affairs experience in an industry-related ...
... highly skilled and experienced Regional Regulatory Affairs Director (EMEA) to join our ... role thanks to your extensive Regulatory Affairs CMC experience, strong leadership, innovative ...
Study Start Up Associate I & II (Site Activation Associate) - Mexico - Homebased ICON ... Role: Study Strat Up Associate II (Site Activation Associate) Summary: Participate on clinical trial ... set Understanding of regulatory and submission processes in many ...
... bring: As a Site Management Associate at ICON you will be ... Update Clinical Management Systems,local regulatory tasks protocol amendments submissions packages ... of ICH-GCP and applicable regulatory requirements. Advanced English level (oral ...
... program development, submission strategies and regulatory interactions in a broad range ... challenges in clinical trials, and regulatory guidance As a world-class ... avoid them. Thorough understanding of regulatory guidance and practices pertaining to ...
... implementation of all Medical Affairs evidence generation projects aligned with ... and expectations of key stakeholders (Regulatory bodies, HCPs, Patients caregivers, Payers, ... industry inclusive of Medical Affairs. Experience with late-stage clinical ...
... , including Clinical Budget Management and Regulatory Affairs Facilitate Informed Consent Form review ... internal groups (Legal, Medical Monitors, Regulatory Affairs, etc.) as well as external ...
... Affairs. Support, update and maintain the ... master file, regulatory binder, source documents, and investigational product ordering, shipping, and associated documentation The Clinical Operations Senior Clinical Research Associate (CRA) is responsible for ...
... Affairs. Support, update and maintain the ... master file, regulatory binder, source documents, and investigational product ordering, shipping, and associated documentation The Clinical Operations Senior Clinical Research Associate (CRA) is responsible for ...