Ph3Overview /h3pAll Job Posting Locations: Milano, Italy /ppIn Johnson Johnson crediamo che la salute sia tutto. Il nostro impegno nell’innovazione sanitaria ci consente di costruire un mondo in cui le malattie complesse vengono prevenute, trattate e curate, in cui i trattamenti sono più intelligenti e meno invasivi e le soluzioni sono personalizzate. /ppAt Johnson Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. /ppLearn more at /ph3Job Information /h3pbJob Function /b: Medical Affairs Group /ppbJob Sub Function /b: Medical Affairs /ppbJob Category /b: Scientific/Technology /ppbLocation /b: Milano, Italy /ph3Role and Responsibilities /h3ulliFor the Milan (MI) site, Johnson Johnson Innovative Medicine seeks a bMEDICAL AFFAIRS MANAGER EMATOLOGIA /b for permanent hire in the Medical Affairs Directorate. /liliDesign and supervise clinical research activities (interventional/non-interventional, local and international) in the therapeutic area of competence, ensuring compliance with ICH-GCP, SOPs, company policies and applicable regulations, and adherence to timelines and budgets. /liliAssess strategic-scientific feasibility of each project; manage the scientific aspects of Medical Affairs studies, including product safety; plan study timelines and modalities, with execution managed by the GCO department; ensure communication of research results (clinical study reports, publications, conferences, Investigator’s meeting). /liliProvide medical-scientific contribution and support to business areas, ensuring SOP and policy compliance and regulatory adherence. /liliOrganize scientific training for Field Force, coordinate scientific information for physicians, prepare documentation (scientific materials, symposium planning, Medical Education events), review research proposals, and verify scientific content in projects; review or draft scientific documentation for regulatory purposes (expert reports, clinical study reports) and for HE MAR activities (Health Economics, Market Access and Reimbursement). /liliPublic relations and institutional cooperation: collaborate with Medical Lead to manage relations with key stakeholders (Ministry of Health, Farmindustria, scientific societies, patient associations); address issues with authorities and clinicians on relevant projects. /liliEMEA-level collaboration (Europe Middle East Africa) to develop global strategy; participate in international team meetings and projects and contribute to identifying new areas for development or product use. /li /ulh3Background and Qualifications /h3pbAcademic and Professional Background /b /pulliDegree in medico-scientific disciplines. /lili4–5 years of prior experience in Medical Affairs in oncology-hematology with experience in multiple myeloma; prior clinical research experience; practical knowledge of GCP; design and development of clinical studies in oncology-hematology. /liliFluent English. /li /ulpbInformation Technology /b /pulliProficiency with MS Office (Word, Excel, PowerPoint). /li /ulpbLocation /b: Based in Milan /ppNote: Please submit your application in English (resume). /ph3Required Skills /h3pbPreferred Skills: /b /pulliAnalytical Reasoning, Clinical Research and Regulations, Clinical Trials Operations, Coaching, Collaboration, Communication, Critical Thinking, Data Analysis, Data Savvy, Digital Culture, Digital Literacy, Healthcare Trends, Medical Affairs, Medical Communications, Medical Compliance, Product Development Lifecycle, Report Writing, Stakeholder Engagement, Technologically Savvy /li /ul /p #J-18808-Ljbffr