
Medical Science Liaison
Posted Sep 2

Posted Sep 2
This is a fully remote position, open to applicants in Kentucky, +4 more states.
β’ Build and nurture robust relationships with key opinion leaders (KOLs) while supporting the scientific and clinical strategy for Orca Bioβs innovative allogeneic cell therapies.
β’ Act as a reliable scientific partner between Orca Bio and external healthcare providers, investigators, and other healthcare professionals within the assigned territory.
β’ Take an active role and contribute to Medical Affairs Strategic Objectives projects.
β’ Offer scientific insights related to stem cell transplantation, cell therapy, cellular immunotherapy, clinical operations, patient access, and the competitive landscape.
β’ Identify, cultivate, and sustain peer-to-peer relationships with academic experts, thought leaders, healthcare professionals, and access stakeholders.
β’ Develop and maintain a territory management plan for Medical Leadership and internal stakeholders.
β’ Assist in the onboarding of treatment centers, adverse event reporting, out-of-spec product handling, and local payer medical education.
β’ Evaluate scientific trends, identify evidence gaps, and recognize research opportunities pertinent to Orca Bio therapies.
β’ Act as the primary liaison for the Investigator-Sponsored Trial program, supporting concepts, protocols, review committees, study oversight, publications, and results dissemination.
β’ Collect and relay scientific insights and stakeholder feedback to leadership and cross-functional partners.
β’ Engage in advisory boards, investigator meetings, roundtables, educational events, professional organizations, advocacy groups, GPOs, networked practices, and speaker bureaus.
β’ Aid in clinical trial patient recruitment, enrollment, and ensure the safe and effective use of investigational products in compliance with GCP.
β’ Lead the collection, analysis, synthesis, and dissemination of congress and scientific-exchange information.
β’ Convert clinical trial data, competitive intelligence, and stakeholder feedback into actionable recommendations.
β’ Provide support for health outcomes, real-world evidence, and strategies for payer/provider engagement.
β’ Implement projects involving research, clinical development, commercial, market access, regulatory, and quality functions.
β’ Educate and train commercial marketing and sales teams regarding therapies and disease states.
β’ Advanced clinical degree in a life science or basic science field (MD, DO, PharmD, NP, PA, DNP, M.Sc, or Ph.D.) with industry experience as an MSL.
β’ Extensive clinical and/or industry experience in malignant hematology, hematopoietic stem cell transplant (HSCT), cellular therapy, CAR-T, immune effector cell therapies, and/or other advanced therapeutic modalities.
β’ In-depth understanding of the cell therapy ecosystem, including operations at transplant centers, apheresis and cell processing workflows, treatment center authorization, patient referral pathways, and competitive cell therapy products.
β’ Strong grasp of clinical development, regulatory requirements, and commercial strategies; familiarity with HEOR data is advantageous.
β’ Exceptional interpersonal and communication skills, with the ability to engage and influence a diverse range of stakeholders.
β’ Proven capability to interpret and present complex scientific data to varied audiences.
β’ Strong strategic thinking, problem-solving abilities, and a solution-oriented approach.
β’ Demonstrated success in collaborating with cross-functional colleagues to effectively meet the needs of both internal and external stakeholders.
β’ Ability to work autonomously and manage multiple priorities within a fast-paced, dynamic environment.
β’ 5+ years of industry experience as an MSL (preferred experience).
β’ Proven experience with field medical launch planning, execution, and post-launch support.
β’ Direct experience supporting cell therapy, stem cell transplantation, CAR-T, or other advanced therapeutic platforms.
β’ Experience in a small biotech company or start-up environment.
β’ Candidate must reside in Ohio (preferred), Pennsylvania (preferred), Indiana, Kentucky, or West Virginia.
β’ Pre-IPO equity.
β’ Annual bonus.
β’ Medical benefits.
β’ Dental benefits.
β’ Vision benefits.
β’ Paid Time Off (PTO).
β’ 401(k) plan.
β’ Life and accidental death and disability coverage.
β’ Parental leave benefits.
β’ Subsidized daily lunches and snacks at on-site locations.
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