Senior Medical Science Liaison, Lymphoma – Lacutamab

Sobi - Swedish Orphan Biovitrum AB (publ)

. Serve as a field-based scientific expert on cutaneous T-cell lymphoma and lacutamab .

Posted 10/14/2026full-timeRemote • Pennsylvania • United StatesSenior💰 $215,000 - $230,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in cutaneous T-cell lymphoma and lacutamab, with a strong ability to build scientific relationships and communicate complex clinical information effectively. Proven experience in medical strategy execution, stakeholder engagement, and evidence generation within the biopharmaceutical industry.

Highest-signal resume keywords

MSL ExperienceHematology-Oncology BackgroundCTCL KnowledgeProject Management SkillsRegulatory Compliance Understanding

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Scientific CommunicationClinical Data AnalysisEvidence GenerationStakeholder MappingMedical EducationProduct Launch ExperienceClinical Practice KnowledgeResearch CollaborationTerritory PlanningPatient Pathway Analysis

Soft Skills

Relationship BuildingStrategic ThinkingProblem-SolvingAdaptabilityEmotional Intelligence

Certifications & Qualifications

Accredited Doctorate Degree

Industry Keywords

Cutaneous T-Cell LymphomaLacutamabBiopharmaceutical IndustryRare DiseaseClinical PracticeDermato-OncologyMedical AffairsCross-Functional CollaborationCompliance RequirementsPatient Advocacy

About the role

Key responsibilities & impact

Serve as a field-based scientific expert on cutaneous T-cell lymphoma and lacutamab
Build trusted scientific relationships with opinion leaders, healthcare professionals, medical organizations, investigators, and other stakeholders
Exchange balanced medical information on CTCL, lacutamab, clinical data, disease biology, treatment approaches, and the care landscape
Respond to unsolicited scientific inquiries and connect stakeholders with Sobi resources
Identify, document, and share field insights on unmet needs, clinical practice, patient pathways, evidence gaps, stakeholder perspectives, competitive developments, and treatment landscape
Partner with Medical Affairs leadership and cross-functional colleagues to inform medical strategy, tactics, educational priorities, and engagement plans
Execute territory-level medical plans aligned with US CTCL and lacutamab medical strategy
Support institution and stakeholder engagement planning
Contribute to lacutamab launch preparedness through disease-state education, scientific exchange, stakeholder mapping, and approved medical tactics
Provide 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 communicate key updates internally
Collaborate to identify and develop CTCL and lacutamab field resources and scientific materials
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 other research collaborations
Partner with Medical Affairs, Medical Information, Clinical Development, Market Access, Patient Advocacy, Commercial, Legal, Compliance, and other functions
Serve as a scientific resource to internal stakeholders and contribute to cross-functional initiatives
Lead territory planning, stakeholder prioritization, documentation, follow-through, and multiple projects
Share best practices and support the broader Field Medical organization

Requirements

What you’ll need

Accredited doctorate degree in a life-science, health-science, or basic-science discipline, such as PharmD, PhD, DNP, DSc, MD, or DO
Candidates with another advanced health degree and extensive relevant industry or clinical experience may be considered
At least 5 years of MSL experience in hematology/oncology or a closely related therapeutic area is highly preferred
Experience in rare disease and/or product launch is highly preferred
Experience in clinical practice, CTCL, lymphoma, dermatology, or dermato-oncology is valued
Strong ability to understand, critically evaluate, and clearly communicate complex scientific and clinical information
Hematology-oncology background is highly preferred
Knowledge of CTCL and the multidisciplinary care environment is an advantage
Demonstrated ability to initiate and sustain credible scientific relationships and respond effectively to key stakeholders
Excellent written, verbal, presentation, facilitation, and listening skills
Demonstrated success working 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, comfortable in a dynamic environment
High personal integrity, sound judgment, and emotional intelligence
Understanding of legal, regulatory, and compliance requirements of the biopharmaceutical industry
Strong commitment to patient needs and advancing scientific understanding within the CTCL community
Frequent domestic travel capability by ground and/or air, 60% or more
Ability to attend local, regional, and national meetings, including occasional evening or weekend programs
Ability to work effectively from a remote office and manage a geographically dispersed territory

Benefits

Comp & perks

Competitive compensation
Generous time off policy
Opportunity to attend popular conferences
Emphasis on work/life balance
Collaborative and team-oriented environment
Competitive 401(k) match
Tuition reimbursements
Wellness reimbursements
Comprehensive medical, dental, and vision package
Additional recognition awards
Short-term bonuses
Long-term bonuses
Remote work arrangement
Company culture focused on rare-disease patient impact