Medical Director

Job title: Translational Science, Associate Director Location: Gaithersburg, MD. Are you a visionary expert in translational science, with the ability to execute a successful strategy in accelerating the development of therapies for patients with immune‑mediated diseases? If you are passionate about transforming the treatment of immune‑mediated diseases and making a profound impact on patients’ lives, then AstraZeneca might be the place for you! Our ambition is to build an extraordinary organization that accelerates the delivery of transformative therapies for patients with immune‑mediated diseases. We are driven by courage, curiosity, and collaboration, making bold decisions driven by patient outcomes. As a Translational Science Associate Director, you will be responsible for the implementation of translational and biomarker objectives for cellular, biologics, and small molecule therapies for immune‑mediated diseases. Your focus will be on ensuring effective collaborations between research and development, establishing strong target‑to‑disease connections, differentiating AZ therapeutics, and driving translational understanding of clinical trial data. You will oversee translational study strategy and deliverables with CROs and collaborators to support new and ongoing clinical studies as well as to enable our life‑cycle management strategy and new program strategies as a global product team level translational lead. You will be recognized as an authority in translational science and work on complex therapeutic projects and scientific problems, providing solutions that are highly innovative. Essential Skills/Experience PhD or MD‑PhD degree in a relevant field required. Degree or training in Immunology preferred. 3 or more years of industry or 5 yrs combined academic/industry experience in clinical development or translational science. Strong knowledge of the pathogenesis of immune mediated disease and the application of cellular, molecular technologies and models to drive program decisions, Prior experience in clinical biomarker strategy development and execution including human target validation, target engagement, and molecular differentiation. Significant experience managing CROs for translational studies and biomarkers for clinical trials. Detailed understanding of translational and clinical research methodology and biostatistics principles. Attention to detail, strive to generate high-quality work, and sense of passion and urgency to achieve team and program goals. Demonstrated experience contributing to and leading complex projects. Demonstrated track record in delivering results. Outstanding verbal and written communication skills. Excellent analytical, problem solving and strategic planning skills. Desired Skills/Experience Experience in clinical biomarker development of T‑cell therapy and/or other advanced therapeutic modalities in house or with CROs Experience in the authoring of relevant sections of regulatory documents. Understanding of the full drug development process, with experience across phases of therapeutic development and studies Understanding of FDA, EMA, MHRA and ICH GCP guidelines as they pertain to translational strategy. The annual base pay (or hourly rate of compensation) for this position ranges from $135,058.40 - 202,587.60 USD Annual. Our positions offer eligibility for various incentives—an opportunity to receive short‑term incentive bonuses, equity‑based awards for salaried roles and commissions for sales roles. Benefits offered include qualified retirement programs, paid time off (i.e., vacation, holiday, and leaves), as well as health, dental, and vision coverage in accordance with the terms of the applicable plans. Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form. #J-18808-Ljbffr