Cluster/Country Clinical Research Manager - Italy Senior Manager

Work Your Magic with us!

Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.

United As One for Patients, our purpose in Healthcare is to help create, improve and prolong lives. We develop medicines, intelligent devices and innovative technologies in therapeutic areas such as Oncology, Neurology and Fertility. Our teams work together across 6 continents with passion and relentless curiosity in order to help patients at every stage of life. Joining our Healthcare team is becoming part of a diverse, inclusive and flexible working culture, presenting great opportunities for personal development and career advancement across the globe.

Your role: 

You will be accountable for day-to-day activities of all aspects for the management of local and/or regional company sponsored studies, including study plans, timelines, resources, allocation, and management of product (re-) supply, problem identification and resolution, status reports and budget to ensure timely delivery of completed study reports to the project teams; accountable for the oversight of Investigator Sponsored Studies or Collaborative Research Studies granted by the Company including the operational assessment of investigator-sponsor, tracking of performance and monitor budgets according to approved plans managing product supply (if applicable), coordinating internal review of final report; manage External providers and/or independent consultants including Contract Research Organization (CRO), Functional Service Provider teams, clinicians, etc.) when required by the project including and not limited to, oversight of the activities and coordination of project specific training, etc.; develop and monitor study budget and timelines; monitor work to ensure quality; ensure that trial status is accurate and up to date in Clinical Trial Management System. You will contribute to the planning and set-up of a study and provide planning parameters; support early access programs on the country level; provide product expertise and/or oversight at the country level to external consultants and/or flexible staff working on company sponsored clinical studies; may be assigned one or more Subject Matter Expert (SME) roles within CDPC or GDO functions (e.g., Lead at the Country level early access programs in collaboration with the Program Clinical Delivery Lead). 

Who you are: 

• Bachelor's Degree in a Medical or Life Science discipline (essential); PhD desirable
• Experienced in understanding of local / country and regional requirements for clinical trials 
• Experienced in managing and steering external providers 
• Networking skills to represent the company to key local stakeholders
• Proactive issue monitoring and management
• Experienced in managing the budget for all local clinical studies in own country, regional study in own hub, and Global Phase IV studies as well as the Investigator Sponsored Studies/Collaborative Research Studies (ISS/CRS) grants
• Fluent in English and Italian 

What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We celebrate all dimensions of diversity and believe that it drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!
 
Apply now and become a part of our diverse team!