
Medical Director β North America
Posted 5 days ago

Posted 5 days ago
This is a fully remote position, open to applicants in United States, +1 more country.
β’ Develop and implement MADxβs medical and clinical strategy for the US and Canada, with senior Director-level accountability, defined priorities, and measurable deliverables.
β’ Initiate, manage, assess, and publish clinical and performance studies.
β’ Propel scientific and clinical initiatives from conception to execution and follow-up.
β’ Build and maintain peer-to-peer relationships with allergists, immunologists, laboratory directors, pathologists, and clinical biochemists.
β’ Establish clinical partnerships and collaborate with key opinion leaders for joint studies and research initiatives.
β’ Formulate and drive healthcare reimbursement and market access strategies for the US and Canada.
β’ Support FDA and Health Canada processes, clinical evaluations, and clinical requirements throughout the product lifecycle.
β’ Collaborate with Regulatory Affairs, Quality Management, R&D, and Product Management teams.
β’ Evaluate the adequacy of clinical evidence and escalate any identified gaps or potential patient-safety concerns.
β’ Represent MADx at scientific conferences and participate in international committees such as CLSI.
β’ Review and approve clinical and medical content, including clinical and performance evaluation reports.
β’ Serve as the primary medical contact for physicians, clinics, and laboratories.
β’ Coordinate medical topics across the organization.
β’ Provide clinical and medical support and training to external clinicians.
β’ Medical degree (MD) with significant clinical expertise in allergy, immunology, or a closely related discipline.
β’ Comprehensive understanding of allergy diagnostics and clinical practice.
β’ Established professional network in the US and/or Canada, preferably including allergists, immunologists, clinical institutions, laboratories, laboratory directors, pathologists, scientific societies, and key opinion leaders.
β’ Experience in clinical or performance evaluation.
β’ Proven track record in planning, conducting, assessing, and publishing clinical or performance studies.
β’ Strong knowledge of applicable regulatory requirements and standards for IVDs and clinical studies, particularly FDA regulations, the US regulatory framework, and Health Canada as well as relevant Canadian provincial regulations.
β’ Ability to critically evaluate clinical evidence and make well-informed medical decisions.
β’ Proactive, self-motivated, and collaborative, with a strategic, hands-on approach, strong ownership, and the capacity to independently translate scientific opportunities into actionable initiatives and measurable results.
β’ Excellent networking, stakeholder management, communication, and presentation skills while interacting with medical professionals and cross-functional stakeholders.
β’ Experience in project planning and management; comfortable working in a dynamic, expanding international organization.
β’ Fluent in English; proficiency in French is a plus.
β’ 10+ years of experience in allergy, immunology, or the diagnostics industry is a strong advantage, ideally with experience in molecular allergy diagnostics or multiplex technologies.
β’ Full-time permanent position.
β’ Flexible working hours.
β’ Remote or hybrid working model available in the US or Canada.
β’ Opportunity to influence MADxβs medical and clinical strategy in North America.
β’ Environment that encourages innovation and the development of scientific and clinical initiatives.
β’ A growing international setting rooted in sustainability, equity, diversity, inclusion, and mutual respect.
AbbVie
AbbVie
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