Senior Medical Science Liaison, Lymphoma – Lacutamab

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

📋 Description

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

• Establish and maintain trusted scientific relationships with opinion leaders, healthcare professionals, medical organizations, investigators, and other stakeholders in CTCL.

• Share balanced, scientifically sound information regarding CTCL, lacutamab, clinical data, disease biology, treatment methods, and the evolving landscape of care.

• Interact with academic, community, hematology-oncology, dermatology, and dermato-oncology practices.

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

• Identify, document, and relay field insights on unmet needs, clinical practices, patient pathways, evidence gaps, stakeholder viewpoints, competitive developments, and treatment environments.

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

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

• Assist in planning for institution and stakeholder engagement.

• Contribute to the readiness for the lacutamab launch through disease-state education, articulation of unmet needs, scientific exchanges, stakeholder mapping, and approved medical tactics.

• 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 initiatives.

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

• Aid in the development of CTCL- and lacutamab-specific field resources and scientific documentation.

• Support Clinical Development and Clinical Operations by identifying sites, engaging investigators, facilitating communication, initiating sites, and aiding patient enrollment.

• Identify evidence gaps and research opportunities.

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

• Support investigator-sponsored research and research collaborations.

• Collaborate with Medical Affairs, Medical Information, Clinical Development, Market Access, Patient Advocacy, Commercial, Legal, Compliance, and other functions.

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

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

• Share best practices, support colleagues, and foster a collaborative, respectful, patient-centered culture.

⛳️ Requirements

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

• Consideration may be given to candidates holding another advanced health degree with extensive relevant industry or clinical experience.

• 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 highly preferred.

• Valued experience in clinical practice, CTCL, lymphoma, dermatology, or dermato-oncology.

• Strong capability to understand, 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 initiate and maintain credible scientific relationships.

• Excellent written, verbal, presentation, facilitation, and listening abilities.

• A demonstrated history of successful collaboration with internal and external stakeholders and influencing across cross-functional teams within a matrixed environment.

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

• Self-motivated and adaptable in a dynamic environment.

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

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

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

• Frequent domestic travel by ground and/or air; 60% or more, depending on territory and business needs.

• Availability to attend local, regional, and national meetings, including occasional evening or weekend programs.

• Capability to work effectively from a remote office while managing 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 reimbursement.

• Wellness reimbursements.

• Comprehensive medical, dental, and vision package.

• Additional recognition awards.

• Short-term bonuses.

• Long-term bonuses.

• Remote work arrangement.