As a global medtech company, we are driven by our Vision of changing the trajectory of lives for a new day and our Mission to create ingenious solutions that ignite patient turnarounds. Our relentless commitment to patients and strong legacy of innovation in healthcare are the foundation of our future. If you're looking for a new chance, a new beginning, a new trajectory, LivaNova is where your talent can truly thrive. Join our talented team members worldwide to become a pioneer of tomorrow—because at LivaNova, we don’t just treat conditions — we aspire to alter the course of lives.
Medical Science Liaison Neuromodulation Eastern Europe & Adriatic (m / f / d)
Position Summary
The Medical Science Liaison Eastern Europe & Adriatic Region (MSL EEUA) establishes and maintains peer-to-peer relationships with health care providers, medical and scientific experts, and key opinion leaders (KOLs) in the Eastern Europe and Adriatic region and provides insights from these external stakeholders to internal colleagues for product and market development and life cycle management.
General Responsibilities
- Ensure that HCPs implanting, dosing or prescribing LivaNova Neuromodulation products have undergone the necessary medical education and have the necessary support to provide the highest level of safety and efficacy
- Develop an understanding of the regional landscape including specialties involved in care of patients
- Generate and execute tactical regional plans to provide needs based, value-added support of the medical and scientific community in line with company goals
- Support clinical development initiatives including investigator-initiated research (IIR) and LivaNova-sponsored clinical studies and registries (e.g., site identification, trial recruitment, and presentation of final approved data)
- Collaborate with key internal and external stakeholders on Medical Affairs-led initiatives including publications, advisory boards, medical education (e.g., CME) opportunities, training, and speaker development
- Identify, profile, prioritize and map thought leaders in line with strategic initiatives and goals
- Support external stakeholders with up-to-date medical information, robust disease expertise, and product information, including providing fair and balanced responses to requests for scientific information
- Serve as scientific peer-to-peer resource to external disease experts and internal stakeholders
- Train internal stakeholders on key scientific and medical topics in relevant therapeutic area
- Maintain effective and appropriate communication among internal stakeholders while maintaining full compliance with relevant requirements
- Maintain accurate reporting and documentation of MSL action plans and key performance metrics in SFDC
Skills and Experience
MD in the specialty of Neurology, Paediatric Neurology, Otolaryngology, Psychiatry or Neurosurgery or PhD in the field of Neuroscience or Biomedical EngineeringSome years’ experience in clinical affairs, medical affairs and / or clinical strategy in the medical device or pharmaceutical industryClinical or research experience in target Therapeutic Area(s) highly desirableDemonstrated ability to establish networks and active relationships with Key Opinion LeadersUnderstanding and demonstrated ability to work compliantly in a field-based role, within the medical affairs organization, in collaboration with the commercial organizationDemonstrated ability to embrace responsibilities and to achieve goalsStrong initiative and desire to work as part of a cross-functional teamExcellent time managementEnglish : Excellent verbal and written communication skillDemonstrated ability to work independentlyPro-active team player, flexible, and ability to work in ambiguous situationsUp to 50% travel within the region. Required travel to medical meetings, team meetings, and other group meetings (will require some weekends)What we can offer you
In addition to providing, you with a supportive, inclusive, and collaborative environment where you will feel empowered to take ownership and drive meaningful change, we will reward you with the following :
A dynamic role in an advanced Medical Device environment interfacing with all worldwide regulatory landscapes supporting your professional career growthExposure to a State-of-the-Art medical device development process, in close co-operation with international cliniciansCompetitive base salaryVariable short-term & long-term incentivesRecognition : through our STARS Program, we recognise and celebrate our colleagues’ contributions and achievementsIf you like the sound of the above and feel energised by the idea of joining a great brand at a moment of exciting expansion, please apply now. We look forward to hearing from you!
Welcome to impact. Welcome to innovation. Welcome to your new life.