ARTO
We are seeking an experienced
Senior Medical Director
to lead medical strategy for rare disease and cardio-metabolic programs. This role reports to the VP of Global Medical Affairs and oversees a cross-functional medical team to drive evidence generation, publications, and external engagement. Key Responsibilities Lead and mentor a Medical Affairs team supporting rare disease and cardio-metabolic assets. Develop and execute medical strategies, plans, and communications to support product lifecycle. Partner across research, development, commercial, market access, and patient advocacy functions. Guide Phase IIIb/IV studies and ensure high-quality evidence generation and dissemination. Engage with regulators, key opinion leaders, advocacy groups, and external stakeholders. Qualifications Advanced degree (MD, DO, PhD, or PharmD), ideally with clinical expertise in rare diseases or cardio-metabolic conditions. 6+ years of relevant industry experience, including leadership in Medical Affairs and product launches. Proven track record in evidence generation, cross-functional collaboration, and regulatory interactions. Deep understanding of compliance and global regulatory requirements. Seniority level : Director,
Employment type : Full-time,
Job function : Consulting and Management Note: We are an equal opportunities employer and welcome applications from all qualified candidates.
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Senior Medical Director
to lead medical strategy for rare disease and cardio-metabolic programs. This role reports to the VP of Global Medical Affairs and oversees a cross-functional medical team to drive evidence generation, publications, and external engagement. Key Responsibilities Lead and mentor a Medical Affairs team supporting rare disease and cardio-metabolic assets. Develop and execute medical strategies, plans, and communications to support product lifecycle. Partner across research, development, commercial, market access, and patient advocacy functions. Guide Phase IIIb/IV studies and ensure high-quality evidence generation and dissemination. Engage with regulators, key opinion leaders, advocacy groups, and external stakeholders. Qualifications Advanced degree (MD, DO, PhD, or PharmD), ideally with clinical expertise in rare diseases or cardio-metabolic conditions. 6+ years of relevant industry experience, including leadership in Medical Affairs and product launches. Proven track record in evidence generation, cross-functional collaboration, and regulatory interactions. Deep understanding of compliance and global regulatory requirements. Seniority level : Director,
Employment type : Full-time,
Job function : Consulting and Management Note: We are an equal opportunities employer and welcome applications from all qualified candidates.
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