Lead cross-functional market access strategy to optimize access for oncology launch and inline brands.
Partner with subject matter experts to analyze payer coverage, affordability, and industry trends.
Hire and develop a team of experts in US market access to drive sustainable value for patients.
Novartis is a global healthcare company that develops innovative medicines to improve patient lives. They are a large organization with a collaborative, agile culture focused on patient access and empowering employees.
Lead and oversee global drug development programs, ensuring alignment with strategic objectives and key milestones.
Facilitate cross-functional collaboration by coordinating program meetings, tracking decisions, and managing risks.
Drive effective decision-making, support budget planning, and mentor stakeholders to enhance operational excellence.
Our partner is a biotechnology or pharmaceutical company advancing innovative therapies through the full drug development lifecycle. They foster a fast-paced, mission-driven environment with cross-functional global teams, focusing on oncology innovation and healthcare impact.
Accountable for translational development strategy from drug candidate through IND submission and Phase 1 entry.
Support biomarker strategies, indication selection, and patient stratification to guide program decisions.
Lead IND-enabling activities, author regulatory documents, and serve as translational science lead in FDA interactions.
We are a small, driven biotech company using Nobel Prize-winning click chemistry to develop targeted cancer therapies that activate potent drugs only at the tumor site. We are a remote-first team encompassing broad backgrounds, united by a mission to make cancer treatments more effective with minimal side effects.
Lead and develop clinical operations teams, overseeing oncology trial execution from feasibility to closeout.
Drive process improvements and operational excellence to enhance study delivery and site performance.
Ensure compliance with regulations, manage budgets and resources, and foster stakeholder relationships.
The company is a global clinical development organization focused on advancing oncology therapies through clinical trials. It fosters a collaborative and inclusive work environment with opportunities for professional growth and continuous learning.
Develop and execute a global training strategy tailored to cell therapy programs across clinical and commercial stages.
Build role-specific onboarding, certification, and continuous learning pathways for Medical and Commercial field teams.
Deliver comprehensive training including disease state education, CAR T product design, clinical data, safety monitoring, and competitive landscape.
Kyverna Therapeutics is a patient-centered, clinical-stage biopharmaceutical company developing cell therapies for autoimmune diseases. It is a scaling biotech environment with a culture driven by core values of collaboration, clarity, innovation, and ownership.
Develop and execute product marketing strategies for oncology portfolio, including product positioning, messaging, and go-to-market plans.
Collaborate cross-functionally with Product Management, Sales, and Marketing teams to drive product launches and commercial execution.
Translate complex clinical data into compelling marketing collateral and engage with key stakeholders to drive product adoption.
BillionToOne is a next-generation molecular diagnostics company that uses proprietary QCT molecular counting technology to enhance disease detection resolution using cell-free DNA, impacting over half a million patients. With over 700 employees and a Great Place to Work certification, the company fosters a transparent, collaborative culture where innovation drives measurable impact and every contribution matters.
Lead evidence generation planning, investigator-sponsored trials, and medical information strategy for a rare disease portfolio.
Drive global medical planning and alignment, integrating AI into Medical Affairs workflows.
Oversee expanded access programs, build scalable operating models, and ensure compliance across all medical activities.
BridgeBio pioneers a 'moneyball for biotech' approach, pooling early-stage research projects to reduce risk and advance rare disease treatments. They value curiosity, experimentation, and ethical use of AI, fostering a culture of pushing boundaries and empowering teams to solve problems.
Develop and execute strategic account plans across health systems, IDNs, and treatment centers.
Lead treatment center activation, onboarding, contracting, operational readiness, and site certification.
Serve as the primary customer contact for CAR-T/cell therapy operations, logistics, and order management.
Kyverna Therapeutics is a patient-centered, clinical-stage biopharmaceutical company developing cell therapies for patients with autoimmune diseases. The company is guided by core values and is committed to transforming the future of treatment for autoimmune disease.
Lead end-to-end TMF strategy, including transition from outsourced to in-house operations.
Ensure TMF health and inspection readiness through governance, quality control, and metrics.
Serve as TMF subject matter expert and partner cross-functionally for document flow and compliance.
Kyverna Therapeutics is a patient-centered, clinical-stage biopharmaceutical company developing cell therapies for patients suffering from autoimmune diseases. The company is guided by core values of collaboration, innovation, and ownership, and is committed to transforming treatment for autoimmune disease.
Provide strategic leadership and oversight for the Neuroscience PAL field team, setting priorities and driving performance.
Develop and nurture key customer relationships, mining insights to translate into internal action.
Build future infrastructure and models to support new product indications and evolving patient access needs.
Bristol Myers Squibb is a biopharmaceutical company dedicated to transforming patients' lives through science, with a focus on oncology, neuroscience, hematology, immunology, and cardiovascular disease. With one of the most diverse and promising pipelines in the industry, the company fosters a culture of passion, innovation, and inclusion, empowering employees to contribute to meaningful change.
Lead design and execution of clinical trials for novel antibody-based therapies in rheumatology and I&I diseases.
Collaborate cross-functionally with clinical operations, regulatory, translational science to ensure robust study designs and data quality.
Interpret clinical data and present findings internally and externally, supporting regulatory submissions and scientific publications.
Spyre Therapeutics is a clinical-stage biotechnology company developing next-generation therapies for immunology diseases. As a small, young company, it fosters a fast-paced, collaborative culture focused on advancing meaningful medicines for patients.
Lead the execution of national clinical education programs and manage cross-functional teams.
Drive customer success strategies and ensure operational excellence across multiple specialties.
Manage budgets, KPIs, and stakeholder relationships to achieve program objectives.
The partner company is a healthcare technology organization that delivers clinical education and adoption programs to improve patient outcomes. The company operates nationally with a collaborative culture and a focus on customer success.
Provide strategic leadership and medical expertise for clinical development of antibody portfolio in IBD.
Lead ongoing Phase 2 platform study and shape registrational program.
Drive cross-functional collaboration and regulatory interactions for global submissions.
Spyre Therapeutics is a clinical-stage biotechnology company developing next-generation therapies for immunology. It is a young, fast-paced company with a high-growth environment, focused on advancing antibody therapeutics for IBD.
Independently manage all operational aspects of Phase I clinical trials from startup through closeout, ensuring adherence to protocols and regulations.
Oversee CROs and vendors to ensure alignment with study goals, budget, and timelines.
Lead the company-wide rollout of Veeva Vault, serving as a primary operational user and subject matter resource.
Absci is a clinical-stage biotechnology company leveraging generative AI for drug discovery through its Integrated Drug Creation platform. The company has a global presence with offices in the US, Switzerland, and Serbia, and fosters a collaborative, innovative culture.
Lead operational execution of cell therapy trials from startup through close-out, managing timelines, budgets, and vendor oversight.
Ensure compliance with regulatory standards including FDA, EMA, and ICH-GCP, and contribute to protocol development and study documents.
Collaborate cross-functionally with clinical operations, data management, regulatory, and manufacturing teams to drive study success.
Kyverna Therapeutics is a patient-centered, clinical-stage biopharmaceutical company developing cell therapies for autoimmune diseases. They are guided by core values of collaboration and innovation, fostering a culture of ownership and clarity.
Designs and leads a comprehensive field manager development program spanning new manager onboarding to advanced leadership curricula.
Builds and manages a high-potential identification and development framework for field talent.
Evaluates and integrates external leadership development resources and measures program effectiveness.
Azurity Pharmaceuticals is a privately held specialty pharmaceutical company focused on innovative products for underserved patients. The company's success is driven by a talented, dedicated team that brings science and commitment to quality.
Lead the full scope of Biostatistics activities for assigned clinical programs, including study design, analysis, and regulatory submissions.
Collaborate cross-functionally with Clinical, Medical, and Regulatory teams to ensure quality and timely delivery of statistical outputs.
Oversee CROs and internal teams, supervise statistical programming, and drive continuous improvement in biostatistics processes.
Mineralys Therapeutics is a clinical-stage biopharmaceutical company focused on developing medicines to target hypertension and related comorbidities. The company is headquartered in Radnor, Pennsylvania and operates as a fully remote organization.
Lead and maintain integrated project plans, drive cross-functional execution, and facilitate team meetings to ensure accountability and progress.
Proactively identify and manage risks, develop mitigation strategies, and support governance readiness with decision-focused materials.
Partner with cross-functional teams to improve planning, execution, and operational processes in a lean, fast-paced environment.
Definium Therapeutics is a late-stage clinical biopharmaceutical company developing psychedelic-based treatments for psychiatric disorders. The company is publicly traded on Nasdaq and fosters a culture of scientific rigor and innovation.
Inspire and lead the Medical Affairs function, guiding MSLs and teams while fostering trusted scientific relationships with KOLs and stakeholders.
Oversee medical information, medical education, HEOR, publication planning, lifecycle management, and launch strategy.
Partner cross-functionally on the Promotional Review Committee, ensuring compliance and scientific rigor.
ARS Pharmaceuticals is a fast-growing, innovative company dedicated to transforming the treatment of severe allergic reactions with neffy, the first FDA-approved needle-free epinephrine product. Headquartered in San Diego, CA, the company fosters a collaborative, entrepreneurial, and inclusive culture with a commitment to improving patients' lives.
Support and execute commercial marketing strategy for key HCP segments across multiple channels.
Manage projects to ensure deliverables are completed on time, within budget, and aligned with business objectives.
Collaborate with cross-functional teams including Sales, Medical Affairs, and Regulatory to drive strategic alignment.
Sobi is a specialized biopharmaceutical company dedicated to developing and delivering innovative therapies for rare diseases. With over 1,900 employees in more than 30 countries, Sobi fosters a collaborative and team-oriented culture committed to patients and diversity.