
Associate Medical Director, Global Medical Strategy
Posted 2 days ago

Posted 2 days ago
This is a fully remote position, open to applicants in United States.
β’ Assist in the formulation and implementation of global medical affairs strategies and tactical plans for designated assets and indications.
β’ Aid in the annual medical planning process and the establishment of measurable medical objectives, key initiatives, and success metrics.
β’ Monitor, assess, and integrate scientific, clinical, and competitive insights.
β’ Support lifecycle management, launch readiness, and planning for indication expansion.
β’ Identify gaps in evidence and prioritize opportunities for evidence generation.
β’ Contribute to plans for evidence generation, secondary analyses, publications, real-world evidence, and scientific communications.
β’ Establish and nurture relationships with external experts and stakeholders.
β’ Assist in organizing advisory boards, expert consultations, and scientific engagement activities.
β’ Support publication planning, congress initiatives, scientific narratives, communication platforms, and materials for medical education.
β’ Ensure scientific accuracy, consistency, and alignment across all medical affairs deliverables.
β’ Represent Medical Affairs on cross-functional asset teams and strategic initiatives.
β’ Collaborate with Commercial, Clinical Development, Regulatory, Global Integrated Evidence & Innovation, Market Access, and other departments.
β’ Lead assigned medical affairs projects and workstreams.
β’ Gather and analyze insights from external experts, scientific meetings, emerging data, and the broader treatment landscape.
β’ Convert insights into actionable recommendations and communicate strategic implications to internal stakeholders.
β’ An MD, DO, PharmD, or PhD in a relevant life sciences field is required.
β’ At least 4 years of experience in Medical Affairs Strategy.
β’ Capability to contribute to the development of medical strategy and execute cross-functional initiatives.
β’ Experience in supporting evidence generation activities, scientific communications, publications, and/or engagement with external experts.
β’ Strong understanding of pharmaceutical development, Medical Affairs functions, and relevant industry regulations.
β’ Ability to critically assess and synthesize scientific and clinical data to guide medical and business decisions.
β’ Excellent skills in writing, verbal communication, presentation, and stakeholder engagement.
β’ Capacity to work effectively in a highly collaborative, cross-functional setting.
β’ Strong project management, organizational, and prioritization skills; ability to manage multiple initiatives simultaneously.
β’ Experience in working with external experts, advisory boards, and scientific meetings.
β’ Experience in launch and/or pre-launch phases.
β’ Preferred experience in the psychiatry therapeutic area.
β’ Proficiency in Veeva and Microsoft Office applications is preferred.
β’ Comprehensive medical, dental, vision, and prescription drug coverage.
β’ Basic life insurance provided by the company.
β’ Accidental death and dismemberment insurance.
β’ Short-term and long-term disability insurance.
β’ Tuition reimbursement.
β’ Assistance with student loans.
β’ Generous 401(k) matching.
β’ Flexible time off.
β’ Paid holidays.
β’ Paid leave programs.
β’ Additional company-provided benefits.
β’ Incentive opportunities.
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