Italy CTR Part II Submissions Specialist

Psi CRO is seeking a Regulatory Submissions Specialist to drive CTR Part II submissions for Italy under the EU CTR. The role collaborates with regulatory and ethics teams to coordinate packages, communicate with authorities, and ensure timely, compliant documentation in a hybrid setup near Milan.You will review translations, track documentation flow, and...

Psi CRO is seeking a Regulatory Submissions Specialist to drive CTR Part II submissions for Italy under the EU CTR. The role collaborates with regulatory and ethics teams to coordinate packages, communicate with authorities, and ensure timely, compliant documentation in a hybrid setup near Milan. You will review translations, track documentation flow, and...

PSI is seeking a regulatory affairs specialist to support Italy under CTR.You will prepare and coordinate CTR Part II submission packages for Italy, communicate with authorities and vendors, and track project documentation.This role offers a hybrid working arrangement in the Milan area.Required: scientific university degree, CTR Part II experience for Italy,...

In this role you drive regulatory submissions for Italy under the EU CTR, supporting the startup of studies for novel medicines. You will work within regulatory and ethics teams to coordinate packages, communicate with authorities, and ensure timely, compliant documentation. The position blends regulatory expertise with cross‑functional teamwork in a...

In this role you drive regulatory submissions for Italy under the EU CTR, supporting the startup of studies for novel medicines. You will work within regulatory and ethics teams to coordinate packages, communicate with authorities, and ensure timely, compliant documentation. The position blends regulatory expertise with cross‑functional teamwork in a...

In this role you drive regulatory submissions for Italy under the EU CTR, supporting the startup of studies for novel medicines. You will work within regulatory and ethics teams to coordinate packages, communicate with authorities, and ensure timely, compliant documentation. The position blends regulatory expertise with cross‑functional teamwork in a...

Location: Remote - EuropeLa preghiamo di verificare di possedere il livello di esperienza e le qualifiche adeguate leggendo la panoramica completa di questa opportunità qui sotto.Company: VB SpineVB Spine is expanding its European organization, and we are now finalizing recruitment for our main Regulatory Affairs team. The core team is based in Warsaw,...

ph3About Ravago /h3pRavago is a privately owned international group with more than 60 years of entrepreneurial heritage.Today, we are a global leader in the distribution of polymers, chemicals and life ingredients, as well as recycling and manufacturing activities.With operations in over 55 countries and more than 10,000 employees worldwide, Ravago combines...

ppJoin to apply for the CMC Senior Specialist role at Zambon /p pZambon is a multinational pharmaceutical and chemical company that focuses on innovation and development with the aim to improve the quality of people's health and patients' lives.Based on a valuable heritage but strongly focused on the future, its Vision is "Innovating cure and care to make...