Job Title: DPS – EMEA Sales Associate DirectorLocation: France, Belgium, Netherlands, Germany or Italy are consideredTravel: 30 to 50%Working Pattern: Remote/Site-BasedThe role:This is an exciting opportunity for an experienced commercial professional to join Lonza’s Drug Product Services
In this role you will drive growth for Lonza’s Drug Product Services across the EMEA region by acquiring new business and expanding existing relationships. You will collaborate with Business Development, Global Sales, Account Management, and Marketing to promote
Overview In this role you will drive growth for Lonza’s Drug Product Services across the EMEA region by acquiring new business and expanding existing relationships. You will collaborate with Business Development, Global Sales, Account Management, and Marketing to
Project Manager Transfer Integrations (m/f/d) Department: Global Operations & Production Job ID: 45153 Professional | Permanent | Full-time | Hybrid Our people in Manufacturing & Global Operations share two priorities: getting things done and making things
Job OverviewThe medical department consists of a Chief Medical Officer, Medical Directors, Sr Medical Directors, Medical Writers, and Safety Associates. The Medical Director provides medical and scientific support to clinical research programs, study teams and investigators.
Job SummaryOur clinical activities are growing rapidly, and we are currently seeking full-time, home or office-based Clinical Research Associates to join our Clinical Monitoring team in Italy. This position will work with a team to accomplish
Sr. Site Contracts AssociateIQVIA BiotechItaly - HomebasedIQVIA Biotech partners exclusively with biotech and emerging biopharma companies to support clinical development across all phases and therapeutic areas. agile structure, collaborative culture, and deep therapeutic expertise allow us to
Job SummaryOur clinical activities are growing rapidly, and we are currently seeking a full-time Clinical Trial Site Relationship Coordinator to join our vibrant Clinical Operations team in Italy, Milan. This is a fantastic opportunity to work
When our values align, theres no limit to what we can achieve.At Parexel, we all share the same goal - to improve the worlds health. From clinical trials to regulatory, consulting, and market access, every clinical
Job SummaryOur clinical activities are growing rapidly, and we are currently seeking full-time, home or office-based Clinical Research Associates to join our Clinical Monitoring team in Italy. This position will work with a team to accomplish
Essential Duties and Responsibilities1. Serve as technical lead and actively participate in complex project conceptual and detail design, execution, development, and support activities crossing multiple projects in two or more focus areas*.2. Identify, prepare and present successful
Job title:Value Access & Pricing Manager Specialty CareLocation: Milan, ItalyAbout the jobAs Value Access & Pricing Manager Specialty Care within our Market Access Team, you’ll be responsible for the design, development, planning and implementation of local Market
Job SummaryOur clinical activities are growing rapidly, and we are currently seeking full-time, home or office-based Clinical Research Associates to join our Clinical Monitoring team in Italy. This position will work with a team to accomplish
Job OverviewManage end-to-end delivery of data management services for single/multi-service projects with minimal guidance, ensuring quality deliverables on time and within budget, to customer satisfaction. Provide comprehensive data management expertise to Data Management (DM) team to
Overview In this role you coordinate the operational management of assigned clinical projects to advance Chiesi’s pipeline in line with medical standards. You act as the primary liaison to CROs, providers, and internal stakeholders, ensuring study
Overview As a Technical Lead, you guide complex projects across multiple focus areas, from concept to delivery, ensuring quality, safety, and customer satisfaction. You’ll shape proposals, lead cross-functional teams, and mentor staff while upholding SEL values
Overview In this role you will program and validate outputs (tables, listings, figures) to support data cleaning and statistical analyses for clinical studies, regulatory and market access requests. You will oversee SDTM/ADaM datasets and related documents,
Overview In this role you will lead labeling strategy within Global Regulatory Affairs to align CCDS, dCCDS, USPI and EU SmPC across products. You will influence product development plans, ensure compliant labeling and support commercial opportunities. You’ll
Overview In this role you will drive regional market access for BeOne Medicines, shaping access strategies through engagement with regional payers and hospital stakeholders. You will represent therapeutic areas and portfolio priorities with a focus on
Overview In this full-time role, you join Medpace’s Clinical Monitoring team to support site-based trials in Italy, helping advance clinical development for diverse therapies. You will perform monitoring visits, ensure protocol and regulatory compliance, and contribute to
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