Global Rare Disease Regulatory Specialist EU&INT

On behalf of our Client, Chiesi Farmaceutici, one of the top 50 pharmaceutical companies in the world with more than 80 years of experience in the pharmaceutical and biotechnology industry, IQVIA is looking for this global, rare disease regulatory affairs specialist in EU and INT to join an exciting working environment in a dynamic and international...

IQVIA Italia is seeking a Global Regulatory Affairs Manager (maternity cover) to join an international team in Rome, Italy. The role supports EU and global regulatory strategy and ensures timely submissions across regions. Requirements include 3–4 years in international regulatory affairs, a Master's degree, and fluent English, with strong...

Pharma Point ricerca un/una Regulatory Affairs Specialist – Medical Device per instaurarsi presso la sede di Roma. La risorsa supporterà la preparazione, l'aggiornamento e il mantenimento della documentazione regolatoria relativa a dispositivi medici destinati ai mercati extra-EU. Collaborerà con distributori esteri e funzioni interne,...

Job PurposeThe VP, Medical Affairs, Rare Diseases BU will provide strategic medical leadership and oversight to support the continued growth of the Rare Diseases (RRD) portfolio. S/he will champion patient centricity as key driver of business decisions. Also, this executive will be a spokesperson for Recordati within the scientific community. S/he will...

On behalf of our Client, Chiesi Farmaceutici, one of the top 50 pharmaceutical companies in the world with more than 80 years of experience in the pharmaceutical and biotechnology industry, IQVIA is looking for a Global Regulatory Affairs Manager (fixed-term maternity cover) to join an exciting working environment in a dynamic and international atmosphere. ...

Syneos Health is seeking a Sponsor Dedicated Local Regulatory Associate based in Rome to provide Italian/EU regulatory expertise for a portfolio of rare disease products. The role requires attendance at the Sponsor's offices in Rome and collaboration with internal teams to ensure compliance with local requirements.The ideal candidate will have 2–4 years of...

Clinical Research Physician, Global Rare Diseases Department: GRD Clinical Development Business Area: R&D, Pharmacovigilance & Regulatory Affairs Job Type: Direct Employee Contract Type: Permanent Location: Europe (flexible) – remote or hybrid What you will do Support the clinical team in relevant medical and scientific aspects of the assigned global...

Global Regulatory Affairs Manager-Maternity Cover IQVIA Italia•Emilia-Romagna, Italy On behalf of our Client, Chiesi Farmaceutici, one of the top 50 pharmaceutical companies in the world with more than 80 years of experience in the pharmaceutical and biotechnology industry, IQVIA is looking for a Global Regulatory Affairs Manager (fixed-term maternity...

The Global Clinical Safety Physician is a the senior clinical safety expert and reports directly to the Global Patient Safety Head. The Global Patient Safety Manager is responsible for developing, managing, executing, and overseeing all aspects of the safety programmes for one (or more) pipeline asset(s) throughout the product(s') life cycle. GPSM plays a...