阿斯利康全球研发中国博士后计划


阿斯利康作为以科学为驱动的领先跨国药企,凭借强大的研发实力,在肿瘤、呼吸、自体免疫、心血管、肾脏、代谢、感染性疾病、罕见病等领域持续深耕。我们致力于探索更高效的诊疗模式,为全球及中国患者显著改善治疗结果、提升生活质量。

作为中国本土研发生态圈的引领者,阿斯利康全球研发中国依托全球资源优势,通过与学术机构、临床中心及生物创新企业深度协作,不断拓展基础研究边界。秉承“在中国、携中国、为全球”的愿景,我们持续助力中国医药研发走向世界舞台,赋能全球研发新生态。

为进一步推动人才培养与科研源头创新,阿斯利康于 2023 年启动肿瘤研发中国博士后计划,并于 20263 月正式将其拓展为“阿斯利康全球研发中国博士后计划”,全面覆盖肿瘤、慢性病及罕见病等核心领域,旨在激励新一代科学领袖,将创新思维转化为应对未尽医疗需求的卓越方案。

招募细则:

·       面向对象: 毕业 5 年内的博士后研究人员,或将于当年12月31日前毕业的应届博士生。

·       资源支持: 入选者将获得专项科研经费,并深度触达阿斯利康全球资源库—包括尖端专业知识、新型化合物库、前沿技术工具以及行业顶尖科学家的指导,全方位助力创新构想的落地转化。

年度入选名单将于次年的“阿斯利康中国研发日”正式揭晓。


2026年度中国博士后项目欢迎如下慢性病及罕见病领域的科学命题申请:

心血管、肾脏及代谢 Cardiovascular, Renal and Metabolism

• Clarifying Lp(a)'s role in atherothrombotic events, focusing on comprehensive lipid profiling, predictive biomarkers and interaction pathways

• Multi-omic profiling of visceral adipose tissue (VAT) to delineate its molecular architecture, distinct biomarkers, and master regulatory pathways driving the transition from metabolic health to obesity-related dysfunction

• Characterizing aldosterone profile and related pathway in health population and chronic kidney patients

早期发现 Early Discovery

• Enabling hit discovery technologies and novel modalities to target the undruggable proteins

• Integrated omics data generation in advanced cell models to guide target selection and compound profiling

呼吸 Respiratory

• CT and novel biomarkers in respiratory diseases: Explore CT and novel biomarkers' progonostics application in different risk population segmentation in COPD and NCFBE

免疫 Immunology

IBD - Fibrosis and fistulae in IBD

• Fibroblast heterogeneity; biomarkers to predict development of fibrostenosing CD and/or strictures; pathways to prevent/reverse intestinal fibrosis

• Specific cell type expression and/or characterization of fibroblasts subsets showing and/or predicting responsive to IL-11 / TL1A; and the differentiation between these pathways and that of TGFB

RA – Very Early RA (or Pre-RA) and Difficult to Treat RA

• Clinical characterization, immunoprofiling, and multiomic profiling of VERA subjects to elucidate journey within healthcare system, current treatment patterns, biomarkers to predict progression to established RA; pathogenic pathways and drivers of established RA in VERA;

• Clinical characterization, immunoprofiling, and multiomic profiling of D2T RA to elucidate the burden, current treatment patterns, pathogenic pathways and drivers of D2T RA or multi-drug resistance.

B cell and T cell biology in autoimmune diseases

• Identify surface markers that discriminate autoreactive/pathogenic T cells from physiologic T cell populations across MS, RA, and IBD intervention

• T cell plasticity and immune tolerance; transcriptional regulators of Treg stability and function; engineer of antigen-specific Tregs (TCR/CAR).

• Targets beyond CD20; B cell subsets heterogeneity and novel subsets; identify autoreactive B-cell clones with strategies for selective depletion

罕见病 Rare disease

Rare renal diseases

• Novel drug targets and therapeutic concepts

• Developing predictive and prognosis biomarkers or animal model to identify high-risk progressive patients in IgA nephropathy or crescentic GN with precision treatment approach

• Exploring the underlined pathogenesis in podocyte injury relevant kidney disease especially related to complement pathway and could be validated with available compounds

• Studying complement or non-complement mediated pathophysiology and disease progression of genetic kidney disease and ANCA-Associated Vasculitis

• Characterizing predictive biomarkers and patient profiles in transplant related kidney disease especially with relapsed GN post-transplant

Rare neurodegenerative diseases

• Novel drug targets and therapeutic concepts.

• Developing predictive and prognostic complex biomarkers in Glioblastoma which include pathology, radiology and molecular assessments to predict response to immune therapies

• Developing translational biomarkers predictive of response to innovative treatment in neurodegenerative diseases

Rare cardiomyopathies

• Novel drug targets and therapeutic concepts

Enabling therapeutic platforms and technologies for rare diseases:

• Improved methodologies for drug delivery and therapeutic intervention (in vivo CAR-T modification, genomic therapies, ligand-conjugates and T-cell engagers)

• Tissue‑targeted delivery science for rare diseases: Delivery systems and targeting moieties to heart, CNS, kidney, cardiac and skeletal muscle

以上项目申请受理截止日期为2026年5月31日

2025年度中国博士后项目欢迎如下肿瘤领域的科学命题申请:

泛瘤种 Pan tumor

• Investigating liver metastatic microenvironment and exploring the therapeutic targets or pathways to treat liver metastases that have the potential to improve metastatic patients’ outcome

• Studying the elements that lead to patient benefit with TCEs, e.g., i) role of different T cell subtypes; ii) interaction with TME; iii) T cell trafficking/availability

• Discovery of new armoring mechanisms for CAR-T in solid tumors

• The relation between MTAP loss and TME (tumor microenvironment) in solid tumors

• Exploring the tumor heterogeneity, target expression, resistance / sensitivity biomarker and association with TME for ADC therapy

• Study of immunogenic cell death and how this can sensitize immunotherapy

消化道肿瘤 Gastrointestinal Cancer

• Developing predictive and prognostic complex biomarkers in gastric cancer which include pathology, radiology and molecular assessments in response to neoadjuvant immune-therapies

• Exploring the adaptive pathways that underly resistance to KRAS inhibition and potential combination in PDAC (Pancreatic ductal adenocarcinoma)

• Characterizing gastric cancer/ esophageal squamous cell carcinoma-specific surface protein expression and their post-translational modifications

泌尿生殖系统肿瘤 Genitourinary Cancer

• Characterizing the early and metastatic urothelial cancers in China on protein, RNA transcript and genomics levels as it relates to response to immunotherapy

以上项目申请受理截止日期为2025年9月30日

 

申请以上项目请在阅读和签署声明书后,填写申请表格,并将下述申请材料发送至邮箱:Chinascientificalliance@astrazeneca.com,申请材料包括:博士后项目申请书、博士毕业证书(PDF 格式)、近五年两篇学术研究代表作(PDF 格式)、立项声明书、个人信息处理知情同意书。