LAVORO INTERNATIONAL REGULATORY AFFAIRS SPECIALIST PARMA, EMILIA ROMAGNA

Experience required 5 years in regulatory with good knowledge of drug development and regulatory procedures education at least bachelor’s degree in life sciences...

Soft skills customer orientation communication skills proactiveness goal orientation technical skills knowledge of national and international pharmaceutical legislation...

The site manages direct distribution to customers in the french market and exports to other markets, effectively meeting both local and international needs...

Participate to regulatory inspections and customer audits as required... about us based in parma, italy, chiesi is an international research-focused pharmaceutical...

Technical skills knowledge of national and international pharmaceutical legislation (in particular national laws (e... about us based in parma, italy, chiesi is...

Languages fluent english technical skills familiarity with international trademark systems (e... about us based in parma, italy, chiesi is an international research-focused...

About us based in parma, italy, chiesi is an international research-focused pharmaceutical and healthcare group with over 90 years’ experience, operating in 31 countries...

regulatory compliance: ensure all documents comply with the applicable regulatory guidelines and company policies, throughout the documents’ development process...

Strong understanding of gcp, regulatory requirements, and clinical trial methodologies...     collaborate with clinical program leaders, statisticians, regulatory...

Strong understanding of gcp, regulatory requirements, and clinical trial methodologies...     engage with regulatory authorities, external experts, and key...

Strong understanding of gcp, regulatory requirements, and clinical trial methodologies...       outstanding communication skills with ability to interact with...

Stay current with regulatory guidelines and industry trends related to patient engagement and innovation in clinical research...  we are looking for real team players...

Stay updated with the latest industry trends and regulatory changes...     deep knowledge of international pharmacopoeia (usp, phr eur, etc)     proficiency...

Ensure cpms maintain compliance with internal sops, gcp, and regulatory standards... strong knowledge of ich-gcp, clinical trial lifecycle, regulatory requirements...

Author, review or approve pharmacometrics reports and related sections of regulatory documents; participate in meetings with clients and regulatory agencies...

About us based in parma, italy, chiesi is an international research-focused pharmaceutical and healthcare group with 90 years’ experience, operating in 31 countries...