629 English-speaking jobs in Milan

Associate Clinical Trial Manager (PhD) role for Infectious Disease/Immunology. Requires a PhD in Life Sciences to manage clinical trial activities, collaborate on global studies, and maintain project timelines.

Associate Clinical Trial Manager (PhD) role in Neuroscience/Ophthalmology. Requires a PhD in Life Sciences to manage clinical trial activities, collaborate on global studies, and maintain project documentation.

Seeking a Dermatologist - Medical Director to provide medical, scientific, and strategic leadership for clinical trials. This role involves medical expertise, study report contribution, and developing new clinical projects. An M.D. degree is required.

Account Executive Small Enterprise owns business accounts, building C-level relationships to deliver outcome-based solutions. Responsibilities include executing account strategies, expanding share-of-wallet, and managing profitability across a full product portfolio.

The Print Sales Specialist specializes in sales, managing account relationships, and providing expertise on HP's products. This role focuses on achieving sales quotas, developing proposals, and landing new logos.

Electrical Commissioning Engineer for Data Centres. Key duties include safe testing, commissioning, and energisation of critical LV and HV electrical systems. Experience with UPS, generators, and power distribution is required.

Mechanical Commissioning Engineer needed for Data Centre projects. Responsibilities include testing and validating HVAC, chilled water, and ventilation systems, and producing commissioning documentation. Experience with complex mechanical systems is required.

Associate in Environmental Law & Town Planning within the Public Law and Regulatory group. Requires an Italian Law Degree (min 105/110), Italian license, and 2-3 years PQE in Town Planning. High level of English is required.

Associate role in Project, Energy and Infrastructure within Banking and Finance. Handle high-profile domestic and cross-border transactions, including project financing, M&A, and due diligence. Requires Italian Law Degree, Italian license, and 3 years PQE.

Senior Site Contracts Associate manages contract strategy and oversees start-up contracting for complex clinical studies. Requires 5+ years of international site contracting experience and expertise in clinical trial regulations.

Experienced Clinical Research Associate needed to perform site selection, monitoring, and close-out visits. Responsibilities include supporting recruitment plans and managing regulatory submissions. Requires relevant degrees, CRA Certification, and pharma/clinical trial experience.

Lead complex global clinical trials in Renal, Obesity, and MASH. Accountable for successful delivery, managing timelines, budgets, and quality while partnering with sponsors. Requires 7+ years of clinical research experience.

Executes feasibility, site identification, regulatory, start-up, and maintenance activities for investigative sites. Prepares and manages site documentation, reviews contracts, and tracks site performance metrics. Requires a Bachelor's in Life Sciences and 1-3 years of relevant experience.

Perform site monitoring and management to ensure study compliance with protocol, GCP, and ICH guidelines. Responsibilities include tracking recruitment, managing documentation, and evaluating site practices. Requires a Master's in Life Sciences and CRA certification.

Medical Director in Oncology provides medical and scientific support for clinical research programs. This role involves medical oversight as a Medical Monitor, reviewing protocols, and managing safety data. Requires a medical degree and 10 years of relevant experience.

Lead a Pharmacovigilance function, managing a team and ensuring high-quality PV and medical information delivery. Requires significant PV experience, people management, and knowledge of European regulations.

Perform site monitoring and management to ensure study compliance with protocol and regulations. Responsibilities include site visits, tracking recruitment, and maintaining study documentation. Requires 3+ years of on-site monitoring experience.

Plan and conduct independent clinical (GCP) audits to assess compliance with regulations and procedures. Prepare findings reports and provide consultation on regulations and policies. Requires certification for audits in Italy and 3+ years in QA Audits.

Principal SoC Design Lead to support global product development for BMS and 48V automotive products. Responsibilities include design execution from kick-off to tape-out, architecture proposal, and IP integration. Requires 10+ years in IC development with analog/mixed-signal expertise.

Senior Consultant supervises Consultants on project work plans and manages client engagements. Responsibilities include reviewing and testing credit risk and financial models, developing solutions, and training team members. Requires a relevant Bachelor's degree and 3+ years of experience.