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A leading biopharmaceutical company is seeking an Associate Director in Medical Affairs to support the development of strategies for multiple sclerosis and pipeline drugs. The role involves collaboration with various teams and requires experience in medical affairs, strong communication skills, and a graduate degree in a health-related field. The position is remote, offering significant interaction with key opinion leaders and healthcare professionals, and contributes to strategic data generation efforts.
Title: Associate Director, Medical Affairs
Location: Remote – United States
If you are interested in the below position, please send your resume tocareers@tgtxinc.com and REFERENCE THE POSITION TITLE within the subject line.
TG Therapeutics is a fully integrated, commercial stage, biopharmaceutical company focused on the acquisition, development and commercialization of novel treatments for B-cell diseases. In addition to a research pipeline including several investigational medicines, TG has received U.S. Food and Drug Administration (FDA) approval for BRIUMVI (ublituximab-xiiy), for the treatment of adult patients with relapsing forms of multiple sclerosis (RMS), to include clinically isolated syndrome, relapsing-remitting disease, and active secondary progressive disease, as well as approval by the European Commission (EC) and the Medicines and Healthcare Products Regulatory Agency (MHRA) for BRIUMVI to treat adult patients with RMS who have active disease defined by clinical or imaging features in Europe and the United Kingdom, respectively. TG Therapeutics is headquartered in Morrisville, North Carolina. For more information, visit www.tgtherapeutics.com .
The Associate Director of Medical Affairs will report to the Director, Medical Affairs, with a focus on multiple sclerosis and pipeline.The individual will support the development and execution of the multiple sclerosis and pipeline medical strategy and help drive data generation, medical communication, and insight generation that is aligned with the company’s goals and meets the needs of the US healthcare market through collaboration with Field Medical, Commercial, Clinical Development, Regulatory, and other cross functional teams.
– – Participate in and contribute to internal discussions focused on MS and pipeline strategy and data generation plans.
– – Assist the team lead in developing and executing disease specific and new indication strategies and tactics with appropriate use of existing and newly created resources.
– – Support team lead to incorporate field medical insights into data generation strategies and to support product launches and lifecycle management of pipeline assets.
– – Lead and support select data generation efforts or research projects to address data gaps and ensure the effective dissemination of the data generated via interaction with and training of field medical teams.
– – Participate in and drive new resource creation, including the creation and review of congress abstracts, posters, presentation slides, manuscripts, educational materials, and advisory board meeting materials.
– – Lead the execution of virtual field medical advisory boards in collaboration with field medical directors, leadership, and medical operations functions
– – Be a strong partner with US Key Opinion Leaders (KOLs), healthcare professionals, and patient advocacy groups to gather insights and inform data generation. Attend field meetings as requested by field medical team to support research discussions.
– – Maintain a thorough understanding of disease biology, scientific data, and competitive landscape in the market; and use the knowledge to support data generation and the refinement of the medical strategy.
– – Work as appropriate with legal, compliance, and regulatory functions to ensure all projects meet regulatory and compliance standards
– – At least 2 years of experience in medical affairs, clinical development, or related roles within the biotechnology or pharmaceutical industry.
– – Experience in translating and discussing medical/clinical information
– – Familiar with the US healthcare system, including regulatory requirements, payer landscape, etc.
– – Customer focused mindset; product launch readiness experience preferred.
– – Excellent communication and people skills, with the ability to engage a wide range of internal and external stakeholders.
– – Experience working in a dynamic fast-paced matrix environment with a high degree of collaboration and teamwork.
– – Remote based with ability to travel required (~ 25%).
– – Advanced degree in health-related field. Experience in MS/immunology/neuroscience preferred.
TG Therapeutics is an equal employment opportunity employer, and does not discriminate on the basis of race, color, religion, gender, sexual orientation, gender identity or expression, age, disability, national origin, ancestry, genetic information, military or veteran status, pregnancy or pregnancy-related condition or any other protected characteristic.