Medical Science Liaison Emerging Therapies - Medical Affairs And Evidence Generation (Maeg) Int[...]

Detalles de la oferta

Join argenx
At argenx, we build our culture from the collective power of the team and the knowledge that together, we are better.
If you are entrepreneurial, curious and committed to making a difference for patients and thrive on creating solutions for rare autoimmune diseases, then argenx is for you.
Next to a competitive salary with extensive benefits, we offer you the chance to grow and be a part of a team driven by purpose, creativity, innovation and science.
About argenx
argenx is a fast-growing global immunology company committed to improving the lives of people suffering from severe autoimmune diseases.
Thanks to colleagues based in Europe, the United States and Japan, we translate immunology breakthroughs into a world-class portfolio of novel antibody-based medicines.
Position Overview
For the expansion of our INTERNATIONAL Medical Affairs and Evidence Generation team, argenx is looking for a Medical Science Liaison Emerging Therapies, located in Germany, Austria, Belgium, The Netherlands, Italy or Spain.
PURPOSE OF THE FUNCTIONThe Medical Science Liaison Emerging Therapies will focus on communicating clinical data and providing scientific expertise about argenx investigational products and compounds in development, in a strictly scientific, non-promotional manner, and in full compliance with argenx policies and procedures.
ROLES AND RESPONSIBILITIESAct as a subject matter expert for pipeline products in preclinical and early-phase clinical stages and be acknowledged internally and externally as an expert.Identify potential high-impact medical research projects and publication opportunities aligned with argenx's objectives.Identify disease-specific KOLs/HCPs to build a cross-specialty KOL map for future indications.Develop and maintain relationships with KOLs for collaboration on research projects and educational initiatives.Supervise experts and centers in defined European countries.Ensure timely scientific/medical exchange and education for HCPs on topics like disease awareness and treatment adherence.Act as a key resource for scientific and clinical questions related to pipeline development.Provide KOLs with the latest clinical data and emerging scientific trends relevant to the pipeline.Initiate and support high-impact medical activities, such as advisory boards and congress symposia.Lead or participate in the training and education of internal teams on therapeutic areas and pipeline assets.Communicate key clinical and scientific findings from ongoing trials to relevant stakeholders.Collaborate on medical strategies for pre-launch and early-stage pipeline products.Attend international congresses and meetings to gather intelligence and develop relationships with important customers.Ensure medical accuracy of Medical Affairs activities and compliance with regulations.SKILLS AND COMPETENCIESAbility to develop and maintain knowledge in complex disease areas.Good understanding of clinical trials and execution.Demonstrated ability to build relationships with external stakeholders.Scientific and customer-centric mindset with a track record of delivering results.Able to problem solve and translate organizational needs into action.Can operate autonomously and assess priorities in real time.Ability to work collaboratively within cross-functional teams.Demonstrated communication skills in a global environment.Agile and adaptable in a dynamic business environment.Project management and proactive planning skills.Ambitious and eager to continuously learn and self-improve.Passionate about contributing to a culture driven by corporate values.EDUCATION AND EXPERIENCEMedical, pharmaceutical or high-level scientific degree (MD, PharmD, PhD).Minimum of 8+ years field-based experience in the biopharmaceutical industry.Proven experience in Medical Affairs is mandatory.Therapeutic area experience in neurology, rheumatology, dermatology, immunology, nephrology, or other rare diseases is an advantage.Experience in clinical R&D is beneficial.Strong understanding of compliance and regulatory landscape.Business fluency in English and at least one other major European language.OTHERAbility for frequent travel (40-60%) as required.Valid driver's license required.The candidate must reside in one of the following countries: Germany, Austria, Belgium, The Netherlands, Italy or Spain.

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Salario Nominal: A convenir

Fuente: Jobleads

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