/Third body/Regulatory Authority submissions are made within the timelines agreed with project management and Site Readiness...Job Overview Primary contact with investigative sites during study maintenance and -when assigned-, site startup...
/Third body/Regulatory Authority submissions are made within the timelines agreed with project management and Site Readiness...Job Overview Primary contact with investigative sites during study maintenance and -when assigned-, site startup...
A clinical research organization in Buenos Aires is seeking an individual to manage regulatory submissions and document...
all that's within you by working in teams of... Site Readiness and Regulatory Specialist I Fortrea Job Overview:Primary contact with investigative...Regulatory Affairs Specialist – Regulatory Affairs / Southern Cone At Johnson & Johnson, the largest healthcare...
all that's within you by working in teams of... Site Readiness and Regulatory Specialist I Fortrea Job Overview:Primary contact with investigative...Regulatory Affairs Specialist – Regulatory Affairs / Southern Cone At Johnson & Johnson, the largest healthcare...
you the opportunity to harness all that’s within you by working in teams of... Site Readiness and Regulatory Specialist...Regulatory Affairs Specialist – Regulatory Affairs / Southern Cone At Johnson & Johnson, the largest healthcare...
stakeholders, and support audit readiness. Idóneo candidates will have experience in multi-site clinical trials and possess... strong knowledge of GCP and regulatory standards. This full-time role is on-site in Buenos Aires, Argentina. #J--Ljbffr...
comply with protocols, Good Clinical Practice (GCP), regulatory guidelines, and organizational standards. The QC Specialist... with study protocols. Conduct regular monitoring visits and ensure adherence to regulatory standards. Support audit readiness...
stakeholders, and support audit readiness. Ideal candidates will have experience in multi-site clinical trials and possess... strong knowledge of GCP and regulatory standards. This full-time role is on-site in Buenos Aires, Argentina. #J--Ljbffr...
QC Specialist collaborates with site staff, Clinical Trial Managers (CTMs), and other departments to verify data accuracy... readiness and collaborate with QA teams during inspections. Train site staff on GCP, documentation practices, and internal...
... Article 6 Readiness Specialist Consultant for Argentina - Capacity Building in Carbon Markets a[...] myGwork - LGBTQ... Readiness Specialist Consultant for Argentina will... Responsibilities: Organize and lead Scrum ceremonies Oversee and manage...