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.
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
Overview As Global NPP Manager, you drive early pipeline assessment and inorganic growth initiatives for the AIR Franchise. You analyze market landscapes, competitive dynamics, and revenue potential to shape investment stories and commercial strategies. You work
Overview In this role, you will lead site management and monitoring for assigned trials to ensure patient safety and high-quality execution. You will work with cross-functional teams to keep study activities on track from activation to
Overview In this Senior Site Contracts role, you’ll own contract strategy and start-up contracting for selected sponsors, enabling complex studies and multi-protocol programs. You’ll work with sponsors, RSU regional teams, and internal partners to ensure timely,
Overview In this role you join Medpaces Clinical Monitoring team in Italy to perform site monitoring, qualification, initiation, and closeout visits while ensuring protocol and regulatory compliance. You will verify investigator qualifications, manage data integrity, and
Overview In this role you support and expand a network of clinical sites in Europe, focusing on feasibility, site selection, and study start-up. You will partner with cross-functional teams to optimize site performance and intelligence, driving
Overview In this role you will lead medical strategy and guidance for neurology programs within ICON, ensuring ethical, compliant and high-impact clinical research. You will collaborate with sponsors, sites, and cross-functional teams to shape protocol medical
Principal Biostatistician (strong Seniors considered) – Global Pharma | Italy (Hybrid) Shape the Future of Drug Development Are you an experienced statistician ready to take your expertise to the next level? Our client, a leading international pharmaceutical company,
Overview As Medical Director you provide medical oversight for clinical trials and serve as the primary medical monitor for sponsor-led studies. You act as the front-line medical resource for project teams, available around the clock to
Overview In this role you lead R&D programs by developing integrated development plans and coordinating cross-functional teams to drive drug development programs forward. You will align Preclinical, Safety, Regulatory, Clinical Operations, and CMC activities, ensuring timely delivery within agreed