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Ascentage Pharma – Who we are: Ascentage Pharma is a global, clinical-stage biotechnology company developing novel therapies for cancer and other diseases. Ascentage Pharma is proud of its collaborative and supportive culture, unified by a shared desire to develop therapeutics that will have a positive impact on patients’ lives. Ascentage Pharma is a dynamic and fast-paced organization that has been responsive to the needs of individual employees throughout its history. The company is defined by a shared understanding that it succeeds in advancing its mission only as each experience’s success in their role.Focusing primarily on protein-protein interaction inhibitors and therapies for hematologic malignancies and solid tumors (including our lead assets like Olverembatinib and Lisaftoclax), this role supports commercialization to maximize global revenues and patient access across the United States and key marketsThe Opportunity: Associate Director, Scientific Publication Writing USThis is an exciting time to join Ascentage Pharma! Ascentage Pharma Group International is a global, commercial-stage, integrated biopharmaceutical company engaged in the discovery, development and commercialization of novel therapies to address unmet medical needs in cancer. We are a globally focused, clinical-stage biopharmaceutical company with a robust portfolio of assets across multiple therapeutic areas. Located in the USA, China and Australia, we are leveraging our expertise in structure-based drug design and our innovative drug discovery engine.Through intensive preclinical investigations, our researchers have developed a robust pipeline of drug candidates that disrupt complex and difficult-to-target protein-protein interactions (PPIs), and next-generation tyrosine kinase inhibitors (TKIs).As our clinical and corporate activities rapidly expand, we seek a highly competent individual to join our growing Medical Affairs Department in support of our ongoing clinical trials.Position OverviewAs Associate Director, Scientific Publication Writing, you will develop and lead the global medical communication of our assets and contribute to the creation of scientific communication plans, publication strategy, and tactics, as well as supporting development of field medical educational material and external tools in alignment with the SVP & Global Head, Corporate Strategy.Areas of ResponsibilityDevelop materials for oncology-specific assets in accordance with the Global Medical Affairs strategyFormulate scientific communication plans for Ascentage Pharma assets, leveraging the publication/data dissemination plan to create simultaneous and aligned enduring materials and educational activitiesBe accountable for accurate and impactful scientific deliverables including symposia, slide decks, MSL tools, and booth materials, as well as accuracy reviews of non-departmental-driven materials (examples: publications & congress presentations)For all deliverables, collaborate with key stakeholders, including investigators, congresses, and medical experts, and liaise with cross-functional internal team including preclinical, clinical development, pharmacovigilance, and biostatistics.Oversee the development of scientific platforms for Ascentage Pharma assetsLine-edit, fact-check, and style manuscripts (often drafted by non-native English speakers), adhering to current AMA, EQUATOR network, and journal QC guidelines and evincing great attention to detailAssist in the development and execution of innovative tools for internal and external communication, including digitalSupervise timely execution of all deliverables within the Scientific Communication plans for all assetsMaintain a strong understanding of internal and external publication, scientific engagement, and medical education standards globally.Oversee medical education strategy exploring innovative and interactive educational opportunities and executing on educational symposia at congresses as neededDisseminate internally up-to-date scientific data across oncology assets and disease states, including recent publications, landscape, insights, presentations, study-specific information, scientific statements, providing training as needed to medical affairs associatesEnsure awareness of assets internally by developing materials and training toolsEnsure clinical trial awareness materials available to MSLs to supplement trial recruitment activitiesMaximize scientific communication opportunities through the creation of tools and content for advisory boards, medical booths, and externally facing meetingsEducation & ExperienceAdvanced degree: PhD, PharmD, or MDOncology experiencePrior work in a pharmaceutical or communication company focusing on oncologyExperience in developing oncology medical education tools and materialKnowledge of publication guidelines and practices, including AMA, ICMJE, GPP, and EQUATOR, as well as familiarity with electronic platforms to ensure ethically compliant, transparent, and audit-ready reviews of publicationsAbility to interpret, analyze, and organize scientific dataExperience with strategic and tactical publication planning, development of abstracts, manuscripts, and slide decks with strong scientific contentExperience with medical education meetings and digital/social medical deliveryExperience leading and working within cross-functional teamsPreferred QualificationsStrong organizational, planning, and business acumen skillsAbility to prioritize needs and the flexibility to address them when business appropriateAbility to conceptually organize and analyze data, interpret, and synthesize complex clinical and nonclinical statistical reports to derive key outcomes and messages; ability to translate scientific and technical issues for diverse audiencesStrong awareness of compliance issues and guidelines around medical education and publicationsAbility to work with multidisciplinary teams to ensure successful execution of deliverablePrioritize projects effectively and proactively collaborate and communicate at all levels within the companyExperience with innovative tools and electronic communication channels; knowledge of applicable guidance related to the dissemination of scientific evidence to external customersStrong leadership capability with a focus on development of high-performing, integrated teamsExpertise in collaborating with external experts on medical affairs activitiesWork Location & ScheduleLocation Preference: Strongly prefer candidates located in the Washington, DC metropolitan area to optimize overlapping working hours with European teams and internal stakeholders.About Ascentage PharmaAscentage Pharma (NASDAQ: AAPG and HKEX: 6855) is a globally focused, clinical-stage biotechnology company engaged in developing novel therapies for cancers, CHB, and age-related diseases. In January of 2025 Ascentage went public on NASDAQ. In July 2025 we announced that our proprietary novel Bcl-2 selective inhibitor Lisaftoclax has been approved by China’s National Medical Products Administration (NMPA) for the treatment of adult patients with chronic lymphocytic leukemia/small lymphocytic lymphoma. In May of 2026 at ASCO Ascentage Pharma announced that is currently in nine registration trials, four of which are global studies intended for FDA and EMA filings.
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Ascentage Pharma – Who we are: Ascentage Pharma is a global, clinical-stage biotechnology company developing novel therapies for cancer and other diseases. Ascentage Pharma is proud of its collaborative and supportive culture, unified by a shared desire to develop therapeutics that will have a positive impact on patients’ lives. Ascentage Pharma is a dynamic and fast-paced organization that has been responsive to the needs of individual employees throughout its history. The company is defined by a shared understanding that it succeeds in advancing its mission only as each experience’s success in their role.Focusing primarily on protein-protein interaction inhibitors and therapies for hematologic malignancies and solid tumors (including our lead assets like Olverembatinib and Lisaftoclax), this role supports commercialization to maximize global revenues and patient access across the United States and key marketsThe Opportunity: Associate Director, Scientific Publication Writing USThis is an exciting time to join Ascentage Pharma! Ascentage Pharma Group International is a global, commercial-stage, integrated biopharmaceutical company engaged in the discovery, development and commercialization of novel therapies to address unmet medical needs in cancer. We are a globally focused, clinical-stage biopharmaceutical company with a robust portfolio of assets across multiple therapeutic areas. Located in the USA, China and Australia, we are leveraging our expertise in structure-based drug design and our innovative drug discovery engine.Through intensive preclinical investigations, our researchers have developed a robust pipeline of drug candidates that disrupt complex and difficult-to-target protein-protein interactions (PPIs), and next-generation tyrosine kinase inhibitors (TKIs).As our clinical and corporate activities rapidly expand, we seek a highly competent individual to join our growing Medical Affairs Department in support of our ongoing clinical trials.Position OverviewAs Associate Director, Scientific Publication Writing, you will develop and lead the global medical communication of our assets and contribute to the creation of scientific communication plans, publication strategy, and tactics, as well as supporting development of field medical educational material and external tools in alignment with the SVP & Global Head, Corporate Strategy.Areas of ResponsibilityDevelop materials for oncology-specific assets in accordance with the Global Medical Affairs strategyFormulate scientific communication plans for Ascentage Pharma assets, leveraging the publication/data dissemination plan to create simultaneous and aligned enduring materials and educational activitiesBe accountable for accurate and impactful scientific deliverables including symposia, slide decks, MSL tools, and booth materials, as well as accuracy reviews of non-departmental-driven materials (examples: publications & congress presentations)For all deliverables, collaborate with key stakeholders, including investigators, congresses, and medical experts, and liaise with cross-functional internal team including preclinical, clinical development, pharmacovigilance, and biostatistics.Oversee the development of scientific platforms for Ascentage Pharma assetsLine-edit, fact-check, and style manuscripts (often drafted by non-native English speakers), adhering to current AMA, EQUATOR network, and journal QC guidelines and evincing great attention to detailAssist in the development and execution of innovative tools for internal and external communication, including digitalSupervise timely execution of all deliverables within the Scientific Communication plans for all assetsMaintain a strong understanding of internal and external publication, scientific engagement, and medical education standards globally.Oversee medical education strategy exploring innovative and interactive educational opportunities and executing on educational symposia at congresses as neededDisseminate internally up-to-date scientific data across oncology assets and disease states, including recent publications, landscape, insights, presentations, study-specific information, scientific statements, providing training as needed to medical affairs associatesEnsure awareness of assets internally by developing materials and training toolsEnsure clinical trial awareness materials available to MSLs to supplement trial recruitment activitiesMaximize scientific communication opportunities through the creation of tools and content for advisory boards, medical booths, and externally facing meetingsEducation & ExperienceAdvanced degree: PhD, PharmD, or MDOncology experiencePrior work in a pharmaceutical or communication company focusing on oncologyExperience in developing oncology medical education tools and materialKnowledge of publication guidelines and practices, including AMA, ICMJE, GPP, and EQUATOR, as well as familiarity with electronic platforms to ensure ethically compliant, transparent, and audit-ready reviews of publicationsAbility to interpret, analyze, and organize scientific dataExperience with strategic and tactical publication planning, development of abstracts, manuscripts, and slide decks with strong scientific contentExperience with medical education meetings and digital/social medical deliveryExperience leading and working within cross-functional teamsPreferred QualificationsStrong organizational, planning, and business acumen skillsAbility to prioritize needs and the flexibility to address them when business appropriateAbility to conceptually organize and analyze data, interpret, and synthesize complex clinical and nonclinical statistical reports to derive key outcomes and messages; ability to translate scientific and technical issues for diverse audiencesStrong awareness of compliance issues and guidelines around medical education and publicationsAbility to work with multidisciplinary teams to ensure successful execution of deliverablePrioritize projects effectively and proactively collaborate and communicate at all levels within the companyExperience with innovative tools and electronic communication channels; knowledge of applicable guidance related to the dissemination of scientific evidence to external customersStrong leadership capability with a focus on development of high-performing, integrated teamsExpertise in collaborating with external experts on medical affairs activitiesWork Location & ScheduleLocation Preference: Strongly prefer candidates located in the Washington, DC metropolitan area to optimize overlapping working hours with European teams and internal stakeholders.About Ascentage PharmaAscentage Pharma (NASDAQ: AAPG and HKEX: 6855) is a globally focused, clinical-stage biotechnology company engaged in developing novel therapies for cancers, CHB, and age-related diseases. In January of 2025 Ascentage went public on NASDAQ. In July 2025 we announced that our proprietary novel Bcl-2 selective inhibitor Lisaftoclax has been approved by China’s National Medical Products Administration (NMPA) for the treatment of adult patients with chronic lymphocytic leukemia/small lymphocytic lymphoma. In May of 2026 at ASCO Ascentage Pharma announced that is currently in nine registration trials, four of which are global studies intended for FDA and EMA filings.
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