Grow Where You Win At Xillium, we believe your career should be a win, not just a job.  We offer stability, growth, and benefits designed to help you succeed at every stage. As a Virtual Medical Assistant, you will support US-based doctors, nurses, and other healthcare professionals in their clinical practice. You will also provide various frontline patient services and/or back-office tasks while providing administrative support to the client’s operations when needed.

• Design, organize, lead and execute training sessions for care professionals on product knowledge effectively • Ensure patients globally in both clinical trial and commercial settings are treated at the highest standards and if necessary to provide onsite support • Plan, organize, and execute Investigator Meetings, Advisory Board Meetings and other equivalent events and present on behalf of the company as needed • Support research, development and commercialization efforts through collecting and synthesizing observation in the medical field and clinicians’ feedback • Develop robust partnership relationship with HCPs within current and future therapeutic area • Educating employees the insights and information gained from academic papers and conference • Identify challenges for the mid to long-term global R&D and medical communication and propose/execute solutions from medical perspective.

• Provides medical oversight of assigned clinical studies • Interacts with senior management, customers, and project teams to ensure subject safety and scientific integrity of clinical studies • Provides therapeutic area medical input and consultation to internal colleagues and customers • Participates in business development meetings • May participate in scientific meetings, upon request • Performs the duties of Medical Monitor • Provides medical input and oversight in support of the Drug Safety and Pharmacovigilance department • Responsible for protocol design and development, upon request • Provides input into protocol amendments • Develops and delivers project-specific and therapeutic training to project team members and clinical site staff; provides training to customer staff as needed • Provides medical and therapeutic input to Study Start Up, Feasibility, and Subject Identification efforts • This activity includes, but is not limited to, review of Informed Consent Templates and Subject-Facing Materials, and input into site feasibility evaluations • Provides oversight to assigned Medical Scientist staff and Medical Director colleagues to review clinical data • Presents identified trends and issues, and mitigation strategies, to customers and project team members to minimize risks to subject safety or integrity of study data • Provides after-hours medical coverage for clinical studies • Adheres to all enterprise policies, work instructions, standard operating procedures, and project plans • Maintains in-depth knowledge of FDA and worldwide drug development regulations and national and ICH Good Clinical Practice (GCP) guidelines

• Provide expert medical input to guide clinical development, comprehensive evidence generation, launch planning and brand plan execution in relevant indications • Develop and execute ambitious short-term and long-term medical strategies, as key elements of the integrated data generation plan and brand plan. • Accountable for the alignment of all global medical affairs activities in partnership with other cross-functional members of the Indication Development Team • Develop close partnerships with regional and country medical affairs leads/teams, and the regional indication strategy teams and ensure all activities maximise cross-regional impact • Build and maintain close partnership with external experts, in collaboration with regional/country Medical Affairs teams, to bring insight to all activities • Initiate and support high impact medical activities, such as advisory boards, congress symposia and medical research projects • Drive the identification and development of productive collaborations including with healthcare organisations and experts, other important customers and stakeholders and professional organizations • Support strategy development for investigator sponsored studies and assessment of proposals • Partner with scientific communications to support development of publication and medical education strategies • Develop and continuously maintain the highest scientific and medical expertise with relevant diseases and products and be acknowledged internally and externally as an expert • Systematically capture, distil and proactively communicate insights and activities within argenx • Ensure all medical affairs activities maintain the highest standards, comply with applicable pharmaceutical regulations, as well as argenx policies and procedures