174 English-speaking jobs in Emilia-Romagna

Lead Statistical Programmer responsible for SAS programming for clinical and safety data systems. Develop work plans, ensure data integrity, and support regulatory submissions using CDISC standards.

Senior Analytical Scientist specializing in LNP/RNA analytics. Drive analytical development and control strategy for gene editing products, including mRNA-LNP characterization using UPLC/UHPLC, DLS, and LC-MS. Manage CRO/CDMO activities.

The Global New Product Planning Manager will complete strategic commercial assessments to drive early pipeline development and due diligence. Responsibilities include assessing market landscapes, revenue forecasts, and developing investment stories. A medical or scientific background is preferred.

Manage inspections, training, documentation, and site compliance for the Quality Management System. Ensure GMP adherence to FDA and EU regulations while improving quality KPIs. Requires a scientific degree and 5+ years in pharma QA/Production.

Manage GCP compliance, CAPAs, and quality metrics within Global R&D. Execute first and second-party audits and finalize quality documents. Requires 3+ years in Pharma/CRO QA with strong GCP knowledge.

Senior Technical Leader for GRD CMC is accountable for CMC development and IMP supply strategy from nomination to commercial launch. Requires 10+ years in pharma, experience with regulatory interactions (EMA/FDA), and leadership of internal/external teams.

Senior Technical Leader for Protein Biologics Development in GRD CMC. Lead CMC strategies for recombinant protein therapeutics, covering expression, upstream/downstream process development, and quality attributes.

Principal Regulatory Writer for Global Rare Diseases. Author, review, and manage regulatory documents for global health authorities, translating clinical and CMC data into compliant submissions across the product lifecycle.

Lead global post-marketing pharmacovigilance operations, ensuring data quality and compliance for Chiesi's portfolio. Oversee safety data collection, literature review, and stakeholder engagement.

Senior Manager, CMC Regulatory Affairs, Global Rare Diseases. Requires 7+ years of Regulatory CMC experience, 3+ in Biologics/Biopharmaceuticals, and advanced knowledge of global CMC regulations.

Senior Technical Leader in GRD CMC with end-to-end responsibility for CMC strategy, execution, and risk management. Expertise includes analytical method development, validation, and control strategy for biological products.

This role ensures control and validation of software systems in GXP processes. Responsibilities include drafting validation plans, managing changes, and acting as a technical expert in audits. Requires 5+ years in CSV within the pharmaceutical industry.

Define and execute the global publication strategy and tactical plan for all global studies. Ensure timely, compliant dissemination of scientific data via congress presentations and peer-reviewed publications.

Senior Manager to drive R&D digital transformation by designing and implementing data-driven processes using platforms like Veeva Vault. This role orchestrates process excellence, digital innovation, and change management across functions.

Drive global supplier quality oversight and lifecycle management for APIs, packaging, and critical GxP suppliers. Define strategy, governance, and performance monitoring across the supply chain.

Manage pharmacovigilance operations for interventional clinical trials, ensuring compliance with PV legislation. Support safety data collection, process maintenance, and CRO oversight within R&D. Requires a Master's degree and 3+ years in Pharmacovigilance or Clinical Research.

Clinical Partnership Manager to optimize governance and operational models for strategic CRO partnerships. Develop and manage vendor relationships, ensuring high-quality clinical trial delivery and continuous improvement. Requires 8-10 years in Clinical Operations.

Principal Statistician for Global Rare Diseases. Provide statistical expertise for drug development programs, clinical trials, and regulatory submissions. Requires PhD/MSc in Statistics and 10+ years in clinical trials.

Financial Controller supporting the Core Markets Business Unit. Responsibilities include month-end/year-end close, financial reporting, planning, and performance monitoring across international markets. Requires 4+ years in international finance.

Manage the Pharmacovigilance System Master File (PSMF) and ensure compliance with regulatory requirements. Evaluate guidelines, update PSMF documentation, define KPIs, and report on PV system performance. Requires a Master's degree and 5+ years in international Pharmacovigilance.