948 English-speaking jobs in Emilia-Romagna
Environment & Sustainability
- Sanofi
- Rimini
- November 1
Drive site-level EHS compliance and environmental performance within a global biopharma network. Ensure regulatory permit adherence, monitor environmental performance (air, water, waste, GHG), and lead incident investigations.
Environment & Sustainability
- Sanofi
- Piacenza
- November 1
Drive site-level EHS compliance and environmental performance within a global biopharma network. Ensure regulatory permit adherence, monitor environmental performance (air, water, waste, GHG), and lead incident investigations.
Environment & Sustainability
- Sanofi
- Ferrara
- November 1
Drive site-level EHS compliance and environmental performance within a global biopharma network. Ensure regulatory permit adherence, monitor environmental performance (air, water, waste, GHG), and lead incident investigations.
Staff Officer (Information Knowledge Management)
- NATO-OTAN
- Poggio Renatico
- November 1
Lead Information Knowledge Management within the DACCC, shaping IM strategies and training. Responsibilities include standardizing IKM, developing staff training, and coordinating initiatives across NATO working groups. Requires a relevant degree and experience.
Staff Officer (Information Knowledge Management)
- NATO-OTAN
- Ferrara
- November 1
Lead Information Knowledge Management within the DACCC, shaping IM strategies and training. Responsibilities include standardizing IKM, developing staff training, and coordinating initiatives across NATO working groups. Requires a relevant degree and experience.
Financial Accountant
- Welocalize
- Modena
- November 1
Financial Accountant owns the reporting cycle for multiple European entities. Responsibilities include managing revenue, regulatory filings (US GAAP/local), payroll, transfer pricing, and cash flow projections. Requires accounting qualification and 2-3 years of experience.
Financial Accountant
- Welocalize
- Parma
- November 1
Financial Accountant owns the reporting cycle for multiple European entities. Responsibilities include managing revenue, regulatory filings (US GAAP/local), payroll, transfer pricing, and cash flow projections. Requires accounting qualification and 2-3 years of experience.
Financial Accountant
- Welocalize
- Reggio Emilia
- November 1
Financial Accountant owns the reporting cycle for multiple European entities. Responsibilities include managing revenue, regulatory filings (US GAAP/local), payroll, transfer pricing, and cash flow projections. Requires accounting qualification and 2-3 years of experience.
Financial Accountant
- Welocalize
- Ravenna
- November 1
Financial Accountant owns the reporting cycle for multiple European entities. Responsibilities include managing revenue, regulatory filings (US GAAP/local), payroll, transfer pricing, and cash flow projections. Requires accounting qualification and 2-3 years of experience.
Financial Accountant
- Welocalize
- Rimini
- November 1
Financial Accountant owns the reporting cycle for multiple European entities. Responsibilities include managing revenue, regulatory filings (US GAAP/local), payroll, transfer pricing, and cash flow projections. Requires accounting qualification and 2-3 years of experience.
Financial Accountant
- Welocalize
- Piacenza
- November 1
Financial Accountant owns the reporting cycle for multiple European entities. Responsibilities include managing revenue, regulatory filings (US GAAP/local), payroll, transfer pricing, and cash flow projections. Requires accounting qualification and 2-3 years of experience.
Financial Accountant
- Welocalize
- Ferrara
- November 1
Financial Accountant owns the reporting cycle for multiple European entities. Responsibilities include managing revenue, regulatory filings (US GAAP/local), payroll, transfer pricing, and cash flow projections. Requires accounting qualification and 2-3 years of experience.
Clinical Research Associate
- IQVIA
- Bologna
- November 1
Monitor clinical sites to ensure study conduct aligns with protocol, GCP, and sponsor requirements. Responsibilities include managing site communications, tracking regulatory submissions, and maintaining TMF/ISF documentation. Requires experience in Pharma or Clinical Trials.
Clinical Research Associate
- IQVIA
- Modena
- November 1
Monitor clinical sites to ensure study conduct aligns with protocol, GCP, and sponsor requirements. Responsibilities include managing site communications, tracking regulatory submissions, and maintaining TMF/ISF documentation. Requires experience in Pharma or Clinical Trials.
Clinical Research Associate
- IQVIA
- Parma
- November 1
Monitor clinical sites to ensure study conduct aligns with protocol, GCP, and sponsor requirements. Responsibilities include managing site communications, tracking regulatory submissions, and maintaining TMF/ISF documentation. Requires experience in Pharma or Clinical Trials.
Clinical Research Associate
- IQVIA
- Reggio Emilia
- November 1
Monitor clinical sites to ensure study conduct aligns with protocol, GCP, and sponsor requirements. Responsibilities include managing site communications, tracking regulatory submissions, and maintaining TMF/ISF documentation. Requires experience in Pharma or Clinical Trials.
Clinical Research Associate
- IQVIA
- Ravenna
- November 1
Monitor clinical sites to ensure study conduct aligns with protocol, GCP, and sponsor requirements. Responsibilities include managing site communications, tracking regulatory submissions, and maintaining TMF/ISF documentation. Requires experience in Pharma or Clinical Trials.
Clinical Research Associate
- IQVIA
- Rimini
- November 1
Monitor clinical sites to ensure study conduct aligns with protocol, GCP, and sponsor requirements. Responsibilities include managing site communications, tracking regulatory submissions, and maintaining TMF/ISF documentation. Requires experience in Pharma or Clinical Trials.
Clinical Research Associate
- IQVIA
- Piacenza
- November 1
Monitor clinical sites to ensure study conduct aligns with protocol, GCP, and sponsor requirements. Responsibilities include managing site communications, tracking regulatory submissions, and maintaining TMF/ISF documentation. Requires experience in Pharma or Clinical Trials.
Clinical Research Associate
- IQVIA
- Ferrara
- November 1
Monitor clinical sites to ensure study conduct aligns with protocol, GCP, and sponsor requirements. Responsibilities include managing site communications, tracking regulatory submissions, and maintaining TMF/ISF documentation. Requires experience in Pharma or Clinical Trials.

























