Senior Medical Director, Autoimmunity

Summary

Join IGM Biosciences as a Senior Medical Director of Clinical Development, Autoimmunity to help develop, lead, and drive the clinical development strategy of the company's current and future pipeline of Autoimmunity medicines. This person will serve as a key member of the senior management team and actively participate in strategic planning, partnering discussions, and presentations to the Board of Directors.

Responsibilities

• Develop IGM Biosciences' clinical and operational strategy concerning autoimmunity medicines
• Provide medical vision and clinical leadership for the strategy and plan to advance IGM Biosciences’ clinical portfolio to registration and beyond
• Develop required tools, systems, staff, and external relationships to be able to conduct all aspects of the clinical development and registration of the company’s autoimmunity products to the highest industry standard and regularly provide information to the CEO and executive leadership and make recommendations on strategy, planning, and implementation of operations
• Act as a primary spokesperson for the Company’s clinical autoimmunity programs with key opinion leaders at medical and scientific conferences and advisory boards, building and maintaining relationships consistent with the Company’s development and commercial objectives
• Work with the executive team to appraise autoimmunity business development opportunities, undertake due diligence activities, and perform strategic and operational analysis
• Ensure autoimmunity clinical development programs meet quality and safety standards required by medical and regulatory agencies, providing leadership to medical affairs and drug safety/pharmacovigilance
• Collaborate with colleagues in discovery research and preclinical development line functions to move product candidates for entry into clinical investigations
• Work with commercial and business development to evaluate product candidates, determine product indications, and design post-marketing studies
• Represent the Company with regulatory and medical agencies, globally addressing their product portfolio's scientific and medical/health aspects
• Establish, promote, and ensure the team performs to the highest standards in global safety management, as well as quality assurance