• Establish the strategy, direction, and priorities of global safety activities • Accountable for the overall safety profile and all product-related decisions and deliverables for assigned products • Serve as the safety expert of the assigned product(s) and or setting the strategy, direction, and priorities of pharmacovigilance activities in the dynamic field of obesity and related conditions • Manage Safety Directors, Associate Safety Directors, and/or Global Safety Professionals • Accountable for providing strategic oversight, direction and authorship for all major regulatory safety submissions • Lead the safety strategy and Benefit/Risk Management Process for assigned asset(s) across all indications in the portfolio • Safety representative to cross functional meetings in providing strategic input for evidence generation, data review and regulatory documents and responses • Lead and contribute to functional projects for process improvement as needed.

Zenas is a clinical-stage global biopharmaceutical company committed to becoming a leader in the development and commercialization of transformative therapies for patients with autoimmune diseases. Our core business strategy combines our experienced leadership team with a disciplined product candidate acquisition approach to identify, acquire and develop product candidates globally that we believe can provide superior clinical benefits to patients living with autoimmune diseases. Zenas is advancing two late-stage, potential franchise molecules, obexelimab and orelabrutinib. Obexelimab, Zenas’ lead product candidate, is a bifunctional monoclonal antibody designed to bind both CD19 and FcγRIIb, which are broadly present across B cell lineage, to inhibit the activity of cells that are implicated in many autoimmune diseases without depleting them. We believe that obexelimab’s unique mechanism of action and self-administered, subcutaneous injection regimen may broadly and effectively address the pathogenic role of B cell lineage in chronic autoimmune disease. Orelabrutinib is a potentially best-in-class, highly selective CNS-penetrant, oral, small molecule Bruton’s Tyrosine Kinase (BTK) inhibitor with the potential to address compartmentalized inflammation and disease progression in Multiple Sclerosis (MS). Zenas’ earlier stage programs include a preclinical, potentially best-in-class, oral, IL-17AA/AF inhibitor, and a preclinical, potentially best-in-class, oral, brain-penetrant, TYK2 inhibitor. We are seeking top talent who share our commitment to patients and have a track record of success in acquiring, developing and commercializing products across the globe. Our colleagues have an opportunity to engage in a fast-paced learning environment and experience individual and organizational success as we work towards becoming a global immunology and autoimmune disease leader, while living our values of Transparency, Relationships, Urgency, Excellence and Innovation – TRUE Innovation! Territory: MidAtlantic (NY, NJ, PA, OH) Position Summary: The Associate Director, Medical Science Liaisons (MSLs), Rheumatology, at Zenas are the field-based extension of our Medical Affairs department. MSLs are scientifically-trained professionals who possess strong clinical and/or scientific backgrounds whose role is to be a resource of fair-balanced and scientifically-rigorous information to the healthcare community. This position reports to the Executive National Director, US MSLs. Key Responsibilities: - Identify, establish, and maintain professional relationships and dialogue with international, national, regional, and local key opinion leaders and allied healthcare professionals. - Educate healthcare professionals on Zenas’ product portfolio. - Function as a regional medical/scientific resource and work to pair external stakeholder needs with available Zenas resources. - Demonstrate proficiency in delivering educational resources and clinical information in response to an established need/request. - Liaise with investigators to support clinical research activities (investigator-initiated and company sponsored). - Facilitate speaker development and training. - Engage in timely and fair-balanced scientific exchanges with HCPs in a compliant, ethical manner in response to unsolicited requests for information related to Zenas’ products. - Lead, contribute to, attend, and provide scientific support at international, national, regional, and local medical conferences. - Liaise with Clinical Operations to support company-sponsored studies. - Actively participate in advisory boards and clinical investigator meetings. - Gather data to generate insights and competitive intelligence to provide impactful and appropriate feedback to headquarters based on field interactions with healthcare providers, thought leaders, and congress attendance. - Deliver internal educational training sessions for internal stakeholders, including disease state, therapeutic landscape, and product information. - Build and cultivate working relationships cross-functionally with adherence to compliance guidelines. - Engage in continued independent learning within the therapeutic area - Adherence to all company regulatory and compliance policies - Identify & coordinate execution of scientific communication opportunities at national and local congresses - Work closely with the team to identify opportunities to generate and present meaningful data - Provide scientific session, poster or symposium coverage when requested - Attend face-to-face meetings to gain pertinent feedback from experts Qualifications: - Advanced clinical/science degree or health care professional credentials required (MD, PhD, RPh, PharmD, NP, PA, MS or equivalent) - Minimum 3+ years MSL, field-based, or clinical position preferred - Therapeutic area experience preferred - Knowledge of treatment guidelines, clinical research processes, FDA regulations, and Officer of Inspector General (OIG) guidelines preferred - Outstanding interpersonal skills, including building strong working relationships and managing and resolving conflict - Excellent communication skills (written, verbal, listening, and presentation) - Results-oriented - Team oriented - Proven track record of success - Current knowledge & full understanding of all relevant industry, legal, and regulatory compliance guidelines - Commitment to the highest ethical, legal, regulatory, and scientific standards #LI-Remote Zenas is committed to fair and equitable compensation practices. The base salary pay range for this role is $181,600 to $227,000. Actual compensation packages will depend on various factors, including, but not limited to depth of experience, education, skillset, overall performance and/or location. Zenas believes in providing a competitive compensation and benefits package to all employees. Our base salary is just one component of Zenas’ competitive total rewards strategy that also includes annual performance bonus, equity, full range of benefits and other incentive compensation plans. Zenas BioPharma is proud to be an equal opportunity employer. We are committed to fostering an environment where diversity is valued. All qualified applicants will receive consideration for employment based on merit, qualifications and the needs of the business.

Overview: Snapscale is seeking a dedicated US Dental Medical Biller who can work remotely to provide full-time, exclusive support to two dental practices. This role is fully integrated into the client’s internal team, offering professional, concierge-style service to patients while handling appointment scheduling, patient intake, and dental insurance verification. The ideal candidate operates with professionalism, adheres to HIPAA compliance, and communicates as a seamless part of the client’s team. Key Responsibilities: - Phone Coverage & Patient Service: Answer all incoming calls via the client’s VoIP system, greet patients professionally, and route calls or document follow-ups. Provide consistent coverage during business hours while maintaining a local, concierge-style presence. - Appointment Scheduling: Schedule new and existing patient appointments using the Eaglesoft practice management system, coordinating closely with in-office team members to maintain calendar accuracy. - Patient Intake Support: Manage digital intake forms, ensuring new patients submit required information such as medical history and past dental visits. Update records accurately in Eaglesoft. - Insurance Verification: Verify dental insurance for incoming patients, completing full or partial verifications according to practice guidelines. Document and track verifications, ensuring completion before appointments. - Team Integration & Reporting: Communicate regularly with in-office staff to ensure alignment on patient scheduling, intake, and insurance verification. Provide daily snapshots of calls answered, appointments scheduled, and insurance verifications completed. Perks: - Health Maintenance Organization (HMO) - Competitive pay - Government-mandated benefits - 13th month pay - Night differential pay - Internet allowance - Yearly salary increase - Opportunities for career growth and development - Fun and supportive working environment Requirements - 6 months to 1 year of experience as a Dental Medical Biller or in a dental administrative role in the U.S. - Familiarity with dental practice management software, preferably Eaglesoft. - Strong understanding of dental insurance verification and patient intake processes. - Excellent written and verbal English communication skills, with a professional and friendly demeanor. - HIPAA-compliant, with the ability to handle sensitive patient information securely. - Able to work full-time, either onsite or remotely from a verified, secure location using Snapscale-provided equipment. - High level of organization, attention to detail, and ability to follow structured tracking systems. - Customer-service oriented, capable of integrating into the client’s team culture. Metrics & Expectations:  - Number of calls answered daily - Number of new patient appointments scheduled - Completion of insurance verifications prior to appointments

Legend Biotech is a global biotechnology company dedicated to treating, and one day curing, life-threatening diseases. Headquartered in Somerset, New Jersey, we are developing advanced cell therapies across a diverse array of technology platforms, including autologous and allogenic chimeric antigen receptor T-cell, T-cell receptor (TCR-T), and natural killer (NK) cell-based immunotherapy. From our three R&D sites around the world, we apply these innovative technologies to pursue the discovery of safe, efficacious and cutting-edge therapeutics for patients worldwide. Legend Biotech entered into a global collaboration agreement with Janssen, one of the pharmaceutical companies of Johnson & Johnson, to jointly develop and commercialize ciltacabtagene autolecuel (cilta-cel). Our strategic partnership is designed to combine the strengths and expertise of both companies to advance the promise of an immunotherapy in the treatment of multiple myeloma. Legend Biotech is seeking an Associate Medical Director, Insights & Executive Engagements as part of the Medical Affairs team based Remotely. Role Overview The Associate Medical Director, Insights & Engagements, plays a critical role within the Medical Affairs organization supporting the strategic scientific and medical leadership for CARVYKTI. This role is responsible for the design and oversight of structured, centralized insight generation activities that will lead to actionable clinical and scientific insights by engaging with key opinion leaders (KOLs), cell therapy centers, and leading academic institutions and thereby inform the U.S. medical strategy. In addition to contributing to the overall CARVYKTI medical strategy, the Associate Medical Director leads the execution strategy of national and regional insight-generation initiatives, including advisory boards, expert roundtables, and strategic scientific engagements. The individual will also lead the planning and execution of medical engagement activities at major scientific congresses and collaborate with leading U.S. cell therapy institutions on executive scientific projects. AMD will be working in close collaboration with cross-functional colleagues ensuring excellent coordination of all engagement related activities. The role will also support the interpretation and internal communication of emerging safety themes derived from aggregated real world experience, advisory boards, and scientific exchange related to Carvykti. In collaboration with pharmacovigilance and cross-functional partners, the Associate Medical Director will help ensure that safety considerations and real-world clinical experiences are translated into medical strategy recommendations, evidence gaps, and future evidence generation priorities alongside the Real-World Evidence Generation Team. Given the global partnership for CARVYKTI, the Associate Medical Director will work in close collaboration with cross-functional colleagues from Johnson & Johnson to ensure alignment on medical strategy, insight generation, scientific exchange, congress activities, site activation and OOS activities. The role will help facilitate effective coordination across organizations to support the shared goal of advancing scientific understanding and optimal clinical use of CARVYKTI. This position requires strong scientific expertise, strategic thinking, and the ability to engage credibly with leading clinicians, investigators, and institutional leaders in the field of hematologic malignancies and cell therapy and will report directly to the Medical Scientific Director of US MA Strategy. Key Responsibilities Insights Generation & Expert Engagement: - Leads the planning and execution of national and regional insight-generation activities, including Advisory Boards, small-group strategy meetings, scientific exchange sessions with key clinical leaders - Capture, synthesize, and communicate strategic insights from KOLs, treatment centers, and investigators to inform medical strategy and lifecycle planning. - Build and maintain strong scientific relationships with leading U.S. cell therapy institutions and academic experts. - Identify emerging trends, unmet needs, and barriers to CAR-T implementation within treatment centers. Executive Scientific Engagements: - Develop and lead executive-level scientific collaborations with key academic institutions, transplant programs, and CAR-T centers. - Partner with institutional leaders and experts on strategic scientific initiatives and projects designed to address key clinical and operational questions in CAR-T therapy. - Support initiatives that promote thought leadership and scientific dialogue within the U.S. cell therapy ecosystem. Congress Strategy & Execution - Lead Medical Affairs planning and execution for major hematology and oncology congresses - Coordinate CARVYKTI-related medical activities during congress including: Advisory meetings and KOL engagements, Scientific discussions and expert exchanges, Internal insight capture and post-congress reporting - Translate congress findings and expert discussions into strategic insights and actionable recommendations for internal stakeholders. Safety & Medical Governance - Contribute to the scientific monitoring of safety information related to CARVYKTI through expert engagements, congress discussions, and clinical insights. - Capture and communicate emerging safety perspectives from clinicians and treatment centers. - Collaborate with pharmacovigilance, medical safety, and cross-functional teams to ensure appropriate escalation and alignment on safety-related insights. - Support scientific exchange and education related to risk management and safe use of CAR-T therapies. Alliance & Cross-Company Collaboration - Collaborate closely with Medical Affairs Alliance counterparts at to ensure alignment on U.S. medical strategy and key scientific priorities related to CARVYKTI. - Support joint Legend–J&J planning processes including advisory board strategy, congress engagement planning, and key expert interactions. - Facilitate the exchange and synthesis of insights across both organizations to inform medical strategy. - Participate in alliance medical meetings, cross-company working groups, and strategic discussions to support effective partnership execution. - Partner with Field Medical, Clinical Development, HEOR, Market Access, and Commercial teams to ensure alignment on key initiatives and engagements. - Contribute to the identification of evidence gaps and opportunities for real-world evidence or investigator-initiated research. - Support internal insight dissemination and strategic decision-making through clear scientific communication. Decision Making - The Associate Medical Director will typically have the authority to make decisions related to direction, methodologies, approaches in the engagement strategy and execution. They may also make decisions related to project execution, including timelines, milestones and resource allocation within budget. Higher-level approvals are required for those related to significant budget allocations, strategic shifts, or major collaborations that have substantial financial or long-term implications. Requirements - MD, PharmD, or PhD in life sciences, medicine, or a related scientific discipline preferred; other advanced medical degree (NP, PA, etc.) considered. - 3–6+ years of experience in Medical Affairs, Clinical Development, or related roles within the pharmaceutical or biotechnology industry. - Experience in hematology/oncology, preferably multiple myeloma, or cell therapy. - Experience interacting with KOLs, academic institutions, and clinical investigators. - Experience planning or supporting advisory boards, scientific meetings, or congress activities preferred. - Demonstrated success in managing complex projects and working in cross-functional teams in a matrix environment with a results focused attitude. - Excellent written and verbal communication skills, with the ability to translate complex scientific concepts into actionable insights for diverse audiences. - Demonstrated proficiency with the most current computer operating systems, Microsoft Office 2013 (particularly Outlook, Word, Excel, and PowerPoint). - SharePoint, Adobe Acrobat Professional, Concur, Veeva and other PC-based applications. Familiar with AI based platforms including Copilot. #Li-JK1 #Li-Remote Please note: These benefits are offered exclusively to permanent full-time employees. Contractors are not eligible for benefits through Legend Biotech. EEO Statement It is the policy of Legend Biotech to provide equal employment opportunities without regard to actual or perceived race, color, creed, religion, national origin, ancestry, citizenship status, age, sex or gender (including pregnancy, childbirth, related medical conditions and lactation), gender identity or gender expression (including transgender status), sexual orientation, marital status, military service and veteran status, disability, genetic information, or any other protected characteristic under applicable federal, state or local laws or ordinances. Employment is at-will and may be terminated at any time with or without cause or notice by the employee or the company. 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