... documents, ensuring alignment with global regulatory strategies.Oversee distribution and tracking ... labeling content development.Recognize potential regulatory issues, solutions, and opportunities.Show ...
... documents, ensuring alignment with global regulatory strategies.Oversee distribution and tracking ... labeling content development.Recognize potential regulatory issues, solutions, and opportunities.Show ...
... with global Legal and Government Affairs teams to identify regulatory trends and understand the impact of existing and future regulatory requirements. The Regulatory Insights team will utilize these ...
... services within: Medical Information, Pharmacovigilance, Regulatory Affairs and Quality Assurance. PrimeVigilance provides ... literature screening and screening of Regulatory Authority website s (if applicable ...
... activation timelines.Escalates to project manager when site activation timelines are ... Meeting.In collaboration with the Regulatory Affairs group, may oversee activities related to central ethics and regulatory submissions.Ensures collection of required ...
... Acts as a Clinical Trial Regulatory Manager (CTRM) on complex clinical trial projects or programs and may act as a Regulatory Oversight for a key customerAbility ...
... customers reservations to Site Works Manager Coordinator or Project Manager by mean of proper tool ... items identified to Site Works Manager Coordinator or Project Manager by dedicated tool template; Updates ...
... customers reservations to Site Works Manager Coordinator or Project Manager by mean of proper tool ... items identified to Site Works Manager Coordinator or Project Manager by dedicated tool template; Updates ...
... across the globe.The Global Regulatory Submissions Lead (Manager, Regulatory Submissions) will collaborate with peers ... suitably experienced, provide guidance and regulatory expertise on the application of ...
... Acts as a Clinical Trial Regulatory Manager (CTRM) on global projects which ... dossiers in accordance with applicable regulatory requirements.Ability to write scientific ... (customer and or IQVIA).Deliver regulatory training presentations as required.May ...