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Represent Clinical Development at the Global Program Team.</li>\n<li>Maintain awareness of internal and external developments (scientific, clinical, competitive, and regulatory) that could impact the development plan, including attendance at major scientific conferences, participation in competitive intelligence activities, and periodic literature review.</li>\n<li>Support business development activities, such as due diligence and research collaborations, as assigned by manager.</li>\n<li>May serve as the Translational Science lead for one or more programs, as assigned by manager.</li>\n<li>Working as part of a cross-functional team with colleagues representing biostatistics, data management, clinical pharmacology, commercial, regulatory, safety, quality, and project management, or others, as assigned by manager.</li>\n</ul>\n<p><strong>Requirements:</strong></p>\n<ul>\n<li>Physician with MD or foreign equivalent.</li>\n<li>3-5 years of clinical development experience preferably within industry.</li>\n<li>3-5 years minimum experience as a medical monitor for clinical trials required.</li>\n<li>Regulatory experience preferred.</li>\n<li>Track record of publication in peer-reviewed journals, preferably first-authored publications.</li>\n<li>Excellent written/oral communication skills.</li>\n<li>Attention to detail and ability to think strategically.</li>\n<li>Willingness to take on new responsibilities.</li>\n<li>Interest and ability to learn about new therapeutic areas.</li>\n</ul>\n<p><strong>Preferred Qualifications:</strong></p>\n<ul>\n<li>Clinical specialty certification from US or foreign equivalent.</li>\n<li>Advanced knowledge of the assigned therapy area is desired, with the capability to interpret, discuss, and represent trial or program level data.</li>\n<li>3+ years of industry experience in clinical development is preferred.</li>\n<li>Experience for medical responsibilities on a cross-functional team preferred.</li>\n<li>Formal training (certificate or graduate degree) in epidemiology, clinical trials, clinical research, biostatistics is strongly preferred.</li>\n<li>Broad experience in the principles of clinical trial methodology, statistics, data analysis, and interpretation.</li>\n<li>Understanding of general (and specific) therapeutic principles.</li>\n<li>Experience designing and executing industry-sponsored clinical trials.</li>\n<li>Expert in scientific literature searches and weighing of quality peer-reviewed data.</li>\n<li>Experience authoring study essential documents, Clinical Study Reports, and regulatory documents.</li>\n<li>Strong relevant therapeutic area experience.</li>\n<li>Ability to clearly communicate to internal and external stakeholders orally and in writing.</li>\n<li>Experience interacting with varying levels of internal/external management and/or academicians and/or clinicians and/or scientists, etc.</li>\n<li>Strong business acumen: including in-depth knowledge of the multidisciplinary functions involved in a company&#39;s drug development process, e.g., clinical operations, biostatistics, regulatory, commercial operations, etc. and can proactively integrate multiple perspectives into the clinical development process for best end-results.</li>\n<li>Ability to prioritize multiple tasks and goals to ensure completion in a timely manner within budget.</li>\n<li>Ability to think both strategically and tactically.</li>\n<li>Advanced knowledge of the assigned therapy area is desired, with the capability to interpret, discuss, and represent trial or program level data.</li>\n</ul>\n<p><strong>Working at Alexion:</strong></p>\n<p>We&#39;re inspired to think differently, to create better outcomes. By creating an unparalleled employee experience, our organization is equipped to adapt and enrich employees with a productive, engaging, and enjoyable work experience, while accelerating world-class leadership and innovation capabilities that can deliver on our mission.</p>\n<p>Each of us is accountable for delivering innovative medicines and supportive technology with integrity so we can truly understand and better the lives of people affected by rare diseases. Together, we can transform lives every day.</p>\n<p><strong>The Highest Standards:</strong></p>\n<p>By operating with the highest standards of ethics and integrity, we aspire to live up to the expectations of patients, physicians, and ourselves, and to earn trust in our communities.</p>\n<p><strong>Diversity:</strong></p>\n<p>We encourage diversity of backgrounds and ideas. We genuinely care for and respect each other, working together as a high-performing team to deliver extraordinary results while embracing different perspectives.</p>\n<p><strong>Dedication:</strong></p>\n<p>The dedication and passion of our employees enable us to stay focused on what matters most. We push ourselves to achieve the highest level of medical innovation, and to redefine what it means to live with a rare disease.</p>\n<p>In-Office Hybrid:</p>\n<p>This role has an expectation of working in the office a minimum of 3 days a week. When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working</p>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">XML job scraping automation by <a href=\"https://yubhub.co\">YubHub</a></p>","url":"https://yubhub.co/jobs/job_e9935992-bf9","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Clinical Development – Neurology & Genomic Medicine","sameAs":"https://astrazeneca.eightfold.ai","logo":"https://logos.yubhub.co/astrazeneca.eightfold.ai.png"},"x-apply-url":"https://astrazeneca.eightfold.ai/careers/job/563877689959090","x-work-arrangement":"hybrid","x-experience-level":null,"x-job-type":null,"x-salary-range":null,"x-skills-required":["Clinical Development","Neurology","Genomic Medicine","Regulatory Strategy","Clinical Trials","Medical Research","Scientific Literature","Peer-Reviewed Journals","Clinical Study Reports","Regulatory Documents","Translational Science","Biostatistics","Data Management","Clinical Pharmacology","Commercial Operations","Regulatory Affairs","Safety and Quality","Project Management"],"x-skills-preferred":["Leadership","Communication","Strategic Thinking","Problem-Solving","Collaboration","Time Management","Prioritization","Business Acumen","Multidisciplinary Functions","Innovation","Adaptability","Emotional Intelligence"],"datePosted":"2026-04-24T14:15:38.306Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Boston, Massachusetts, United States of America"}},"skills":"Clinical Development, Neurology, Genomic Medicine, Regulatory Strategy, Clinical Trials, Medical Research, Scientific Literature, Peer-Reviewed Journals, Clinical Study Reports, Regulatory Documents, Translational Science, Biostatistics, Data Management, Clinical Pharmacology, Commercial Operations, Regulatory Affairs, Safety and Quality, Project Management, Leadership, Communication, Strategic Thinking, Problem-Solving, Collaboration, Time Management, Prioritization, Business Acumen, Multidisciplinary Functions, Innovation, Adaptability, Emotional Intelligence"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_1e7293b7-e75"},"title":"Applied AI Engineer, Life Sciences (Beneficial Deployments)","description":"<p>We&#39;re looking for an Applied AI Engineer to join our Beneficial Deployments team, focused on maximizing the impact of Claude in the life sciences. 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However, some roles may require more time in our offices.</li>\n<li>Visa sponsorship: We do sponsor visas! However, we aren&#39;t able to successfully sponsor visas for every role and every candidate. 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