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Job Post Details
Job details
Full job description
Location: Northeast
Territory: ME, VT, NH, CT, MA, NY, PA, NJ, MD, DE, RI
If you are interested in the below position, please send your resume to careers@tgtxinc.com and REFERENCE THE POSITION TITLE within the subject line.
Organizational Overview
TG Therapeutics is a fully integrated, commercial stage, biotechnology 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 Therapeutics has received approval from the U.S. Food and Drug Administration (FDA) for BRIUMVI® (ublituximab-xiiy) for the treatment of adult patients with relapsing forms of multiple sclerosis, including clinically isolated syndrome, relapsing-remitting disease, and active secondary progressive disease, as well as approval by several foreign nations for BRIUMVI to treat adult patients with RMS who have active disease defined by clinical or imaging features. For more information, visit www.TGTherapeutics.com.
Role
The Medical Science Liaison (MSL) is a field-based regional Medical Affairs professional responsible for developing and enhancing relationships with medical professionals, researchers, clinical trial support staff, advocacy, and other members of the Myasthenia Gravis (MG) scientific and clinical community. Additionally, the MSL will demonstrate scientific, clinical, and therapeutic area expertise during scientific engagements with key opinion leaders (KOLs) and other healthcare professionals (HCPs) and requires credibility to engage top national and regional thought leaders.
Reporting into the MSL Team Field Director, the MSL is a critical role in TG Therapeutics’ customer-facing field model, collaborating compliantly with cross-functional teams including Clinical Development, Sales, Marketing, and Market Access to provide clinical support and education.
This role will cover the following territory: ME, VT, NH, CT, MA, NY, PA, NJ, MD, DE, RI
Key Responsibilities
- Be a credible medical/scientific expert
- Fair-balanced scientific engagement across the assigned geography; establishes and maintains relationships with KOLs, HCPs, clinics and institutions, payers, and other stakeholders within the MG area
- Responsive and engages regularly with thought leaders and external stakeholders
- Collaborate and support Clinical Development and Clinical Operations research initiatives including site identification and trial recruitment
- Partner with clinical trial sites to optimize patient recruitment strategies, leveraging both data-driven insights and relationship-building
- Collaborate with cross-functional teams—including Clinical Operations, Regulatory Affairs, and Medical Affairs—to troubleshoot recruitment challenges and streamline processes
- Monitor site performance metrics and provide actionable recommendations to improve enrollment rates.
- Support investigator meetings, site initiation visits, and ongoing trial communications
- Maintain compliance with all regulatory requirements and company SOPs while fostering trust and transparency with stakeholders
- Supports Medical Affairs initiatives (advisory board meetings) and informs medical strategy through capturing and reporting of medical insights
- Keeps current on disease state, therapeutic landscape, and competitor data and records insights
- Utilize effective, confident, and professional communications to establish strong relationships with internal and external stakeholders
- Respond to and documents unsolicited medical requests (MIRs) for information in a timely manner
- Support Market Access by educating payers (Health plans and state Medicaids) and key decision makers (Pharmacists and P&T Committees) on the clinical efficacy and safety profile to support formulary decisions
- Liaise unsolicited submissions and information for investigator-initiated trials (IITs) between the investigator and home office Medical Affairs
- Lead and/or participate in special projects or initiatives aligned to US Medical strategy and objectives
- Maintain accurate reporting and documentation of MSL activities
Professional Experience/Qualifications
- A scientific or clinical professional with a passion for science and deep scientific knowledge
- At least 2 years of experience in a Medical Science Liaison or similar role (MG disease experience preferred); will consider candidates with > 5 years of MG clinical experience
- Must have well-established networks and active relationships with KOLs in the MG community
- Strong knowledge of GCP guidelines and clinical trial processes
- Exceptional communication and presentation skills, with the ability to translate complex science into clear, actionable insights
- Energetically embraces responsibilities, demonstrates initiative, and excellent time management
- Agile, adaptable
- A collaborative mindset and genuine passion for improving patient outcomes
- Field-based, with the ability to travel approximately 75%
Education
- Advanced Scientific or Clinical degree (MD, PharmD, PhD, DNP) with a minimum of 2 years of relevant clinical or pharmaceutical experience; NP or PA with 5 or more years clinical experience in MG will be considered. Must reside in the territory.
Applicants must be currently authorized to work in the United States on a full-time basis. The company does not sponsor employment visas for this position.
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.