Senior Medical Science Liaison, Lymphoma – Lacutamab

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

📋 Description

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

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

• Provide balanced medical information regarding CTCL, lacutamab, clinical data, disease biology, treatment options, and the overall care landscape.

• Engage with academic, community, and multidisciplinary practices in hematology-oncology, dermatology, and dermato-oncology.

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

• Identify, document, and communicate field insights on unmet needs, clinical practices, patient pathways, evidence gaps, stakeholder perspectives, competitive advancements, and treatment environments.

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

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

• Assist in planning for institutional and stakeholder engagement.

• Contribute to lacutamab launch readiness through education, stakeholder mapping, and approved medical tactics.

• Provide both internal and external scientific training on CTCL, preclinical science, clinical data, evidence gaps, and outcomes.

• Participate in advisory boards, medical roundtables, webinars, symposia, and other educational opportunities.

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

• Collaborate on developing CTCL and lacutamab field resources and scientific materials.

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

• 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.

• Partner 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 contribute to cross-functional projects.

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

• Share best practices, assist colleagues, and nurture a collaborative, respectful, and 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.

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

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

• Experience in rare diseases and/or product launches is highly desirable.

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

• Strong capacity to comprehend, critically assess, and articulate complex scientific and clinical information clearly.

• A hematology-oncology background is highly preferred.

• Knowledge of CTCL and the multidisciplinary care environment is advantageous.

• Proven ability to establish and maintain credible scientific relationships and respond effectively to key stakeholders.

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

• Demonstrated success in collaborating with internal and external stakeholders and influencing across 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 fast-paced environment.

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

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

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

• Frequent domestic travel, by ground and/or air, of 60% or more.

• Ability to attend local, regional, and national meetings, including occasional evening or weekend events.

• Capability to work effectively from a remote office while managing a geographically dispersed territory.

🏝️ Benefits

• Competitive compensation package.

• Generous time off policy.

• Opportunities to attend prominent conferences.

• Strong emphasis on work/life balance.

• Collaborative and team-oriented workplace environment.

• 401(k) matching program.

• Tuition reimbursement options.

• Wellness reimbursement programs.

• Comprehensive medical, dental, and vision benefits package.

• Additional recognition awards.

• Eligibility for short-term and long-term bonuses.

• Flexibility to work from a remote office.

• Occasional company-supported participation in local, regional, and national meetings, congresses, webinars, symposia, and educational programs.