Associate Director, Bioanalysis (Cell Therapy)

WHY JOIN US? At AstraZeneca, we are dedicated to being a Great Place to Work, where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit. With an ambitious goal of delivering 20 new medicines by 2030, there is no better place to make a difference in medicine, for patients, and in society. Join us on this exciting journey to pioneer the future of healthcare. Our inclusive culture champions diversity and collaboration, and we are always committed to lifelong learning, growth, and development. As part of our team, you’ll contribute to groundbreaking advancements that will shape a healthier future for people everywhere. Be a catalyst for change at AstraZeneca, where your work will have a real impact on improving people’s lives. Introduction to Role Are you ready to make a significant impact in the field of cell therapy? Join our dynamic team at AstraZeneca as an Associate Director within the Cell Therapy Enterprise, where you will lead the design and implementation of robust bioanalytical strategies to support clinical assay endpoints. Your expertise will be crucial in advancing our cell therapy pipeline and transforming the lives of patients. Accountabilities Lead design and implementation of robust bioanalytical strategies to support clinical assay endpoints, including but not limited to PK/CK/PD, immunogenicity (humoral, cellular, viral) and biomarkers related to cell and gene products to support the AstraZeneca cell therapy pipeline (CAR/TCR/in vivo). Identify, evaluate scientific and operational capabilities and establish partnerships with selected specialty laboratories and CROs for generation and analysis of bioanalytical data. Lead and oversee assay development, qualification/validation and tech transfer (when appropriate) of cell therapy‑related bioassays at CROs or using internal capabilities. Interpret and integrate complex datasets within programs and across the cell therapy portfolio. Provide written and verbal updates to key stakeholders. Contribute to publication strategy, prepare data for publication or presentations in internal/external scientific conferences. Essential Skills/Experience PhD degree in immunology, cellular and/or tumor biology or a related field with 7+ years of relevant industry experience with strong background in cell therapy. Demonstrated experience managing/directing analysis of clinical biospecimens to support clinical trials. Proven experience in regulated bioanalysis across a range of modalities PK/CK, PD and immunogenicity assessments. Able to evaluate and interpret complex data sets using analysis and visualization software (i.e. Cytobank/OMIQ/FCS Express, Tableau/Spotfire/JMP), experience with AI tools is a plus. Work cross‑functionally and collaboratively with project stakeholders. Deep understanding of cell therapy biology and up‑to‑date with latest analytical methods applicable to characterization of cell therapy products and mechanism of action. Understanding of global regulatory expectations and analytical requirements to support regulatory filings. Experience managing assay development teams, overseeing tech transfers, scientific quality and study conduct internally and at CROs. Ability to interpret complex datasets and exceptional ability to communicate results verbally, in writing and in presentations adapting to different audiences as required. Ability to prioritize multiple projects and task concurrently in a fast‑paced environment. Pay & Benefits The annual base pay for this position ranges from $135,058.40 to $177,264.15 USD. Base pay offered may vary depending on multiple individualized factors, including market location, job‑related knowledge, skills, and experience. In addition to the base salary, the position offers a short‑term incentive bonus opportunity; eligibility to participate in our equity‑based long‑term incentive program. Benefits offered include a qualified retirement program (401(k) plan); paid vacation and holidays; paid leaves; and health benefits including medical, prescription drug, dental, and vision coverage in accordance with the terms and conditions of the applicable plans. Equal Employment Opportunity Evinova is an equal opportunity employer that is committed to diversity and inclusion and providing a workplace that is free from discrimination. Evinova is committed to accommodating persons with disabilities. Such accommodation is available on request in respect of all aspects of the recruitment, assessment and selection process and may be requested by emailing View email address on click.appcast.io. #J-18808-Ljbffr