934 English-speaking jobs in Emilia-Romagna

Support worldwide post-approval regulatory activities focused on CMC for vaccines or biological products. Develop submission strategies, assess quality changes, and coordinate cross-functional input for regulatory dossiers. Requires Life Sciences education and experience in technical/CMC/quality regulatory affairs.

Senior Regulatory Affairs Associate drives post-approval CMC activities for biologics and vaccines. Responsibilities include developing submission strategies, assessing quality changes, and preparing documentation for variations and renewals. Requires experience in pharma regulatory affairs and CMC.

Senior Regulatory Affairs Associate drives post-approval CMC activities for biologics and vaccines. Responsibilities include developing submission strategies, assessing quality changes, and preparing documentation for variations and renewals. Requires experience in pharma regulatory affairs and CMC.

Senior Regulatory Affairs Associate drives post-approval CMC activities for biologics and vaccines. Responsibilities include developing submission strategies, assessing quality changes, and preparing documentation for variations and renewals. Requires experience in pharma regulatory affairs and CMC.

Senior Regulatory Affairs Associate drives post-approval CMC activities for biologics and vaccines. Responsibilities include developing submission strategies, assessing quality changes, and preparing documentation for variations and renewals. Requires experience in pharma regulatory affairs and CMC.

Senior Regulatory Affairs Associate drives post-approval CMC activities for biologics and vaccines. Responsibilities include developing submission strategies, assessing quality changes, and preparing documentation for variations and renewals. Requires experience in pharma regulatory affairs and CMC.

Senior Regulatory Affairs Associate drives post-approval CMC activities for biologics and vaccines. Responsibilities include developing submission strategies, assessing quality changes, and preparing documentation for variations and renewals. Requires experience in pharma regulatory affairs and CMC.

Senior Regulatory Affairs Associate drives post-approval CMC activities for biologics and vaccines. Responsibilities include developing submission strategies, assessing quality changes, and preparing documentation for variations and renewals. Requires experience in pharma regulatory affairs and CMC.

Senior Regulatory Affairs Associate drives post-approval CMC activities for biologics and vaccines. Responsibilities include developing submission strategies, assessing quality changes, and preparing documentation for variations and renewals. Requires experience in pharma regulatory affairs and CMC.

Clinical Project Leader guides global clinical studies for Large Pharma partners. This role leads cross-functional teams to deliver trials on time and budget, ensuring ICH GCP compliance. Requires CRO experience in Phase I–III trials, strong English, and financial management skills.

Clinical Project Leader guides global clinical studies for Large Pharma partners. This role leads cross-functional teams to deliver trials on time and budget, ensuring ICH GCP compliance. Requires CRO experience in Phase I–III trials, strong English, and financial management skills.

Clinical Project Leader guides global clinical studies for Large Pharma partners. This role leads cross-functional teams to deliver trials on time and budget, ensuring ICH GCP compliance. Requires CRO experience in Phase I–III trials, strong English, and financial management skills.

Clinical Project Leader guides global clinical studies for Large Pharma partners. This role leads cross-functional teams to deliver trials on time and budget, ensuring ICH GCP compliance. Requires CRO experience in Phase I–III trials, strong English, and financial management skills.

Clinical Project Leader guides global clinical studies for Large Pharma partners. This role leads cross-functional teams to deliver trials on time and budget, ensuring ICH GCP compliance. Requires CRO experience in Phase I–III trials, strong English, and financial management skills.

Clinical Project Leader guides global clinical studies for Large Pharma partners. This role leads cross-functional teams to deliver trials on time and budget, ensuring ICH GCP compliance. Requires CRO experience in Phase I–III trials, strong English, and financial management skills.

Clinical Project Leader guides global clinical studies for Large Pharma partners. This role leads cross-functional teams to deliver trials on time and budget, ensuring ICH GCP compliance. Requires CRO experience in Phase I–III trials, strong English, and financial management skills.

Clinical Project Leader guides global clinical studies for Large Pharma partners. This role leads cross-functional teams to deliver trials on time and budget, ensuring ICH GCP compliance. Requires CRO experience in Phase I–III trials, strong English, and financial management skills.

Drive European retail media campaigns for a global advertiser, managing end-to-end efforts across major retailers. This data-driven role requires 4+ years in Paid Media, strong analytical skills, and experience with retail media platforms.

Drive European retail media campaigns for a global advertiser, managing end-to-end efforts across major retailers. This data-driven role requires 4+ years in Paid Media, strong analytical skills, and experience with retail media platforms.

Drive European retail media campaigns for a global advertiser, managing end-to-end efforts across major retailers. This data-driven role requires 4+ years in Paid Media, strong analytical skills, and experience with retail media platforms.