Clinical Project Manager – European Medical Device Studies

Clinical Project Manager – European Medical Device StudiesYour Job Description Summary: Are you ready to combine your expertise in clinical research with your talent for project leadership?Join our European Clinical Affairs team and play a pivotal role in advancing endovascular therapy.As a Clinical Project Manager, you'll lead the planning and execution of clinical studies, ensuring every milestone is met with excellence.From protocol development and regulatory submissions to study reports, you'll orchestrate every detail with precision and purpose.You'll oversee both post market studies and pre market development projects, driving innovation while ensuring patient safety.We're looking for a motivated professional with a life sciences degree, 3+ years of clinical study management experience, and strong communication skills across diverse stakeholders.Hospital experience is a plus.Fluency in English is required, while Italian proficiency will give you an edge for upcoming studies.Remote role with up to 40% (or more during peak times) travel across Europe, based preferably in Italy.Applicants from Germany or France could also be considered.This is your chance to contribute to cutting edge medical device research, grow within a dynamic team, and make a real impact on patient outcomes.Your Key ResponsibilitiesLead clinical study planning and execution to ensure timely, on-budget delivery on high-risk Class III medical devices.Manage projects from protocol development to study reports.Manage contracts, budgets and financial tracking including invoice approvals and accruals.Oversee internal project teams in a matrix organization and external vendors to ensure quality and compliance.Ensure regulatory and procedural compliance with EU-MDR, ISO*****, Good Clinical Practice, applicable European regional laws and standards and with the BD's quality system.Serve as a clinical subject matter expert on cross-functional project teams.Supervise and mentor department personnel as needed.Support trial master files (eTMF) and clinical data systems (CDMS) for clinical documentation and clinical data management.Engage with investigational sites and key opinion leaders (KOLs) to foster collaboration.Support on-site monitoring and participate in cross-functional meetings.Prioritize tasks effectively to meet or exceed project milestones.Manage regulatory submissions to national competent authorities and ethics.Your Profile3>Degree in life sciences (biology, medicine, clinical research) – bachelor's or master's.5+ years of experience in clinical research (medical device, pharmaceutical and/or biotechnology and/or academic clinical research).3+ years' experience in clinical study project management, site management and monitoring within industry or a CRO.Strong project management skills and ability to communicate with diverse stakeholders.Experience in hospital settings is a plus.Languages English: mandatory; and Italian: a strong plus, especially for upcoming studies in Italy.Expect *****% travel.Based preferably in Italy (alternatively in France or Germany).Ready to make an impact in advancing healthcare innovation?Apply now and help us shape the future of endovascular therapySalary Range Information€54,****** - €86,****** EUR AnnualBD is one of the largest global medical technology companies in the world.Advancing the world of healthTM is our Purpose, and it takes the imagination and passion of all of us—from design and engineering to the manufacturing and marketing of our billions of MedTech products per year—to look at the impossible and find transformative solutions that turn dreams into possibilities.We welcome people with the imagination and drive to help us reinvent the future of health.At BD, you'll discover a culture in which you can learn, grow and thrive.And find satisfaction in doing your part to make the world a better place.Becton, Dickinson and Company is an Equal Opportunity Employer.We evaluate applicants without regard to race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, and other legally-protected characteristics.#J-*****-Ljbffr