Gra Eu Spec - Global Regulatory Affairs

Our client, **Chiesi Farmaceutici **- one of the top 50 pharmaceutical companies in the world, with more than 80 years of experience within the pharmaceutical and biotechnology industry - in order to expand their staff, entrusted to IQVIA the recruitment of **GRA Eu Specialist-Global Regulatory Affairs - **who can join an exciting working environment in a dynamic and international atmosphere.
The GRA EU RA Specialist ensures the execution of regulatory plans in the Region EU for the assigned portfolio.
**RESPONSIBILITIES**:
- Support the Business continuity and GMD strategic plans;
- Support the R&D projects cross-functional teams;
- Timely inform and coordinate the EU affiliates, other GRA units (operations and CMC), corporate functions(GMD, GPV, GCD, GMA and global MKTG) and external stakeholders (licensors, partners and licensees) forthe achievement of the assigned task
- Compile and maintain the regulatory databases REQUIREMENTS:
**TYPE OF CONTRACT**:
Maternity Replacement
Chemical contract