
Senior Medical Science Liaison, Lymphoma – Lacutamab
Posted Oct 14

Posted Oct 14
This is a fully remote position, open to applicants in California.
• Act as a field-based scientific authority on cutaneous T-cell lymphoma and lacutamab.
• Cultivate trustworthy scientific partnerships with opinion leaders, healthcare professionals, medical organizations, investigators, and other stakeholders.
• Provide balanced medical information regarding CTCL, lacutamab, clinical data, disease biology, treatment methodologies, and the evolving care landscape.
• Engage with academic, community, and multidisciplinary practices in hematology-oncology, dermatology, and dermato-oncology.
• 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 guide medical strategy and engagement plans.
• Implement territory-level medical plans consistent with the US CTCL and lacutamab medical strategy.
• Assist in planning stakeholder engagement and key institution interactions.
• Contribute to lacutamab launch preparedness through education on disease states, scientific exchange, 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 advisory boards, medical roundtables, webinars, symposia, and educational initiatives.
• Represent Sobi Medical Affairs at scientific and medical congresses and relay key updates internally.
• Collaborate in the development of CTCL and lacutamab scientific materials and field resources.
• Assist Clinical Development and Clinical Operations with site identification, investigator engagement, communication facilitation, site initiation, and patient recruitment.
• Identify evidence gaps and potential research opportunities.
• Contribute to evidence generation, real-world evidence, publications, and medical education programs.
• Support investigator-sponsored research and 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 for internal stakeholders.
• Lead territory planning, stakeholder prioritization, documentation, follow-through, and management of multiple projects.
• Share best practices, support colleagues, and promote a collaborative, respectful, and patient-focused culture.
• Doctorate degree in a life-science, health-science, or basic-science discipline, such as PharmD, PhD, DNP, DSc, MD, or DO is required.
• Candidates with another advanced health degree and substantial 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 highly preferred.
• Experience with rare diseases and/or product launches is highly preferred.
• Background in clinical practice, CTCL, lymphoma, dermatology, or dermato-oncology is valuable.
• Strong capability to comprehend, critically assess, and effectively communicate complex scientific and clinical information.
• A hematology-oncology background is highly preferred.
• Familiarity with CTCL and the multidisciplinary care environment is an advantage.
• Proven ability to establish and maintain credible scientific relationships.
• Excellent written, verbal, presentation, facilitation, and listening skills.
• Demonstrated success in collaborating 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 abilities.
• Self-motivated and adaptable in a dynamic setting.
• High personal integrity, sound judgment, and emotional intelligence are essential.
• Understanding of legal, regulatory, and compliance standards within the biopharmaceutical industry.
• Strong commitment to addressing patient needs and furthering scientific understanding within the CTCL community.
• Willingness to travel domestically by ground and/or air 60% or more.
• 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.
• Competitive compensation package.
• Generous time off policy.
• Opportunity to attend renowned conferences.
• Emphasis on work/life balance.
• Collaborative and team-oriented work environment.
• Competitive 401(k) matching program.
• Tuition reimbursement options.
• Wellness reimbursement programs.
• Comprehensive medical, dental, and vision benefits.
• Short-term bonus opportunities.
• Long-term bonus potential.
• Additional recognition awards.
• Flexible remote work arrangement.
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