Senior Medical Science Liaison, Lymphoma – Lacutamab

This is a fully remote position, open to applicants in Texas.

📋 Description

• Act as a field-based scientific authority on cutaneous T-cell lymphoma and lacutamab.

• Develop trusted scientific relationships with opinion leaders, healthcare professionals, medical organizations, investigators, and other stakeholders.

• Provide accurate, fair, balanced, and scientifically rigorous information regarding CTCL, lacutamab, clinical data, disease biology, treatment methods, and the overall care landscape.

• Address unsolicited scientific inquiries and connect stakeholders with Sobi resources.

• Identify, document, and disseminate field insights on unmet needs, clinical practices, patient pathways, evidence gaps, stakeholder perspectives, competitive developments, and the treatment landscape.

• Collaborate with Medical Affairs leadership and cross-functional teams to inform medical strategy, tactics, educational priorities, and engagement plans.

• Implement territory-level medical plans that align with US CTCL and lacutamab medical strategy.

• Assist in institution and stakeholder engagement planning.

• Contribute to the launch preparedness of lacutamab through disease-state education, articulation of unmet needs, scientific exchange, stakeholder mapping, and execution of approved medical tactics in the field.

• Deliver internal and external scientific training on CTCL disease biology, preclinical science, clinical data, evidence gaps, and outcomes.

• Participate in or support advisory boards, medical roundtables, webinars, symposia, and educational activities.

• Represent Sobi Medical Affairs at scientific and medical congresses and relay key updates internally.

• Identify and create field resources and scientific materials specific to CTCL and lacutamab.

• Support Clinical Development and Clinical Operations with site identification, investigator engagement, communication facilitation, site initiation, and patient accrual.

• Identify evidence gaps and research opportunities.

• Contribute to evidence generation, real-world evidence initiatives, publications, and medical education programs.

• Support investigator-sponsored research and research collaborations.

• Work collaboratively with Medical Affairs, Medical Information, Clinical Development, Market Access, Patient Advocacy, Commercial, Legal, Compliance, and other departments.

• Serve as a scientific resource for internal stakeholders and support cross-functional initiatives.

• Lead territory planning, stakeholder prioritization, documentation, follow-through, and manage multiple projects.

• Share best practices, assist colleagues, and cultivate a collaborative, respectful, patient-focused culture.

⛳️ Requirements

• An accredited doctorate degree in a life-science, health-science, or basic-science discipline, such as PharmD, PhD, DNP, DSc, MD, or DO.

• Candidates holding another advanced health degree with extensive relevant industry or clinical experience may be considered.

• A minimum of 5 years of MSL experience in hematology/oncology or a closely related therapeutic area is highly preferred.

• Experience in rare diseases and/or product launches is strongly preferred.

• Background in clinical practice, CTCL, lymphoma, dermatology, or dermato-oncology is valued.

• Strong capability to comprehend, critically assess, and effectively communicate complex scientific and clinical information.

• A background in hematology-oncology is highly preferred.

• Familiarity with CTCL and the multidisciplinary care environment is advantageous.

• Proven ability to establish and maintain credible scientific relationships.

• Exceptional written, verbal, presentation, facilitation, and listening skills.

• Demonstrated success in working with internal and external stakeholders and influencing cross-functional teams in a matrixed environment.

• Proven strategic thinking, problem-solving, decision-making, project management, and prioritization skills.

• Self-directed and adaptable in a dynamic environment.

• High personal integrity, sound judgment, and emotional intelligence.

• Understanding of the legal, regulatory, and compliance requirements within the biopharmaceutical industry.

• Strong commitment to patient needs and advancing scientific understanding within the CTCL community.

• Willingness to travel frequently by ground and/or air, 60% or more.

• Ability to participate in local, regional, and national meetings, including occasional evening or weekend programs.

• Capability to work effectively from a remote office and manage a geographically dispersed territory.

🏝️ Benefits

• Competitive compensation.

• Generous time off policy.

• Opportunity to attend popular conferences.

• Focus on work/life balance.

• Collaborative and team-oriented environment.

• Competitive 401(k) match.

• Tuition reimbursements.

• Wellness reimbursements.

• Comprehensive medical, dental, and vision package.

• Short-term bonuses.

• Long-term bonuses.

• Additional recognition awards.