Senior Director, National Head, Field Medical Affairs

Role Summary

The Senior Director, National Field Medical Lead is a scientific and clinical expert responsible for advancing medical and scientific exchange related to Calcilytix endocrinology programs. This role leads the national Field Medical Affairs organization, shapes field medical strategy, and ensures consistent, compliant execution in support of launch readiness, external stakeholder engagement, and insight generation.

Responsibilities

• Develop, operationalize, and execute a national field medical strategy aligned to Calcilytix Medical Affairs objectives and program priorities
• Lead field medical launch readiness planning, including field tool development, scientific narrative alignment, and readiness for congress and other high-impact external engagement
• Provide leadership to the field-based Medical Affairs organization, including recruiting, onboarding, coaching, mentoring, and performance development
• Define expectations and quality standards for field excellence (engagement planning, documentation, insight quality, congress execution, and stakeholder follow-through)
• Build and maintain strategic relationships with national and regional endocrinology key opinion leaders (KOLs), investigators, academic centers, specialty clinics, and other influential stakeholders
• Ensure delivery of high-quality, compliant scientific exchange with healthcare providers and external stakeholders, including disease biology, emerging clinical data, trial activity, unmet need, and the Calcilytix pipeline
• Support Calcilytix-sponsored and investigator-initiated research (IIR), including site identification, feasibility input, investigator engagement, and appropriate clinical/scientific support

Qualifications

• Required: Advanced scientific or clinical degree (MD, DO, PharmD, or PhD)
• Required: 8+ years of Medical Affairs and/or Field Medical experience with demonstrated track record of excellence
• Preferred: Background in endocrinology and/or rare disease experience
• Required: Strong communication, presentation, relationship building, organizational, analytical, and interpersonal skills
• Required: Deep understanding of clinical research and pharmaceutical development processes
• Required: Ability to comply with all internal policies and external regulations, including those related to travel, expenses, and compliance
• Required: Comfort working independently in a dynamic, fast-paced environment; 60-75% travel required

Skills

• Communication and presentation
• Relationship building and stakeholder engagement
• Strategic thinking and leadership
• Operational planning and workforce development
• Clinical research literacy and pharmaceutical development processes
• Regulatory and compliance acumen

Education

• Advanced degree required: MD, DO, PharmD, or PhD

Additional Requirements

• Travel: 60-75% travel for KOL engagement, clinical site visits, joint field visits and coaching, internal meetings, and scientific congresses