Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionAt Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future.Our global Clinical Operations colleagues within our PPD clinical research services provide end-to-end support for clinical trials from study start up to monitoring through to study close out, across commercial and government contracts. Together, we help clients define and develop clinical programs, minimize delays, and execute high-quality, cost-efficient clinical studies.The PPD FSP Solution:PPD's Functional Service Provider division partners with and serves as an extension of our PPD team, supporting our customers' key functions. We cover customer needs on every level, allowing them to do more with less, with an uncompromising commitment to quality. We deploy the same top-tier talent in ALL engagement models. Exceptionally trained, rigorously supported and technologically empowered to help customers manage capacity and set programs up for success.Joining within our PPD FSP functional area allows you to join the renowned PPD CRO and still gain invaluable client dedicated experience.Discover Impactful Work:The Medical Science Liaison (MSL) is a field-based expert on scientific data, products, and trials, responsible for engagement with medical stakeholders at Clinical Trial Centers (Kidney Transplant Studies) across the region. The MSL will represent and reflect client values as a science-driven, patient-centric organization. The MSL is critical in understanding the management of diseases of interest, mapping the patient journey, identifying unmet medical needs, data gaps, and areas of collaboration. The MSL will work closely with the Kidney Transplant Clinical Trial Teams. While the focus will be on the region, the function will also support activities and projects across the EMEA region.A day in the Life:Expert medical resource and ambassadorMaintain the highest scientific and medical expertise of all relevant diseases and products; be acknowledged internally and externally as an expert. Focus lies on the Clinical Trials we are conducting in the Transplant TA (DGF and AMR with empa and efgar respectively).Identify and develop productive relationships and collaborations with all relevant stakeholders, including healthcare professionals and professional organizations.Support the development and implementation of the kidney transplant site engagement plan to advance client objectives.Help shape the position of the client in the region.Maintain a high level of knowledge of and appropriately implement current local pharmaceutical regulation and ensure implementation of client policies and procedures.Scientific/medical exchange and education, and insight generationEnsure timely and informative scientific/medical exchanges with external stakeholders that accurately reflect scientific data.Deliver high quality scientific/medical education in a variety of settings, including related to diseases of interest, clinical studies (focus on our DGF trial and in 2nd line AMR Trial), investigational products, and any future licensed products.Obtain feedback that can be disseminated throughout the organization.Coordinate the timely and appropriate response to internal and external Medical Information inquiries, utilizing client medical information resources and in line with regulatory requirements.Attend appropriate local, national, and international meetings and congresses to gather intelligence, develop productive collaborations, engage in scientific exchange, and ensure insights are shared within the client.Cross-functional collaborationEnsure a close working relationship with all client functions: Focus lies on the CTT for the two kidney transplant studies.Support cross-functional teams to ensure operations are patient-focused, including rapidly responding to internal and external requests to discuss specific situations and challenges and provide medical affairs support to all stakeholders.Keys to Success:Entrepreneurial spirit and ability to achieve results independently and partner with colleagues across functions and geographies.Strong influencing skills to be able to engage effectively with stakeholders and within the company.Ability to quickly understand:complex disease areas, treatments, and clinical development plans - Ideally experience in the kidney transplant TA.healthcare landscape, hospitals, healthcare professionals, and patient journey.the broader healthcare policy context including especially market access processes.Demonstrated ability to build productive collaborations with medical experts.Excellent communication skills: verbal, written, and when giving presentations.Proven track record of delivering results that meet or exceed targeted objectives.Ability to work collaboratively and effectively together within cross-functional teams and networks.Demonstrated communication skills, within a multi-cultural and multi-lingual global environment.Is agile and demonstrates adaptability, comfort with ambiguity, trust-building, and resilience.Derives energy from operating in a dynamic, complex, fast-moving, and frequently changing business environment.Demonstrable experience with project management, proactive planning, priority setting, and securing alignment.Drives toward outcomes.Ambitious, inquisitive, naturally a quick study, with demonstrated eagerness to continuously learn, self-improve, and develop. This includes being comfortable giving and receiving feedback in a diverse environment.Passionate and prepared to lead and contribute to our culture, which is driven by our corporate values of co-creation, innovation, empowerment, excellence, and humility.EDUCATION, EXPERIENCEScientific, healthcare, or medical degree (MS, PharmD, PhD, MD, RN, PA).Significant field-based experience in a biopharmaceutical industry in medical affairs.Clinical experience in Medicine (Kidney or other solid organ) is an advantage.Knowledge of regulations and practices related to industry interactions with healthcare professionals.OTHERValid driver's license.Ability for 50% travel.
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