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This role works in close alignment with Global Study Teams and local leadership to ensure that studies are designed, set up, conducted, and closed in full compliance with AstraZeneca Procedural Documents, ICH-GCP and local regulations.</p>\n<p>Ready to shape how complex oncology trials are delivered in practice?</p>\n<p><strong>Accountabilities</strong></p>\n<ul>\n<li>Hold overall accountability for meeting country-level study commitments, ensuring timely delivery of high-quality data.</li>\n<li>Lead Local Study Teams for assigned studies, including CRAs, CSAs and other contributors, promoting collaboration, clarity of roles and strong performance.</li>\n<li>Drive optimal performance and compliance of Local Study Teams with AstraZeneca Procedural Documents, ICH-GCP requirements and local regulations.</li>\n<li>Oversee high-quality clinical and operational feasibility assessments for potential studies, providing robust input into study selection and design.</li>\n<li>Coordinate and manage the site selection process, including identification of potential sites and investigators, initial site quality risk assessments and, where needed, Site Qualification Visits to assess suitability and quality risk.</li>\n<li>Ensure timely submission of applications and documentation to Ethics Committees/IRBs and, in partnership with Regulatory Affairs, support delivery of submissions to Regulatory Authorities in line with local requirements.</li>\n<li>Prepare accurate country-level financial agreements and maintain current study budgets within the clinical financial system, working closely with Director SMM or Director Country Head and Clinical Finance as appropriate.</li>\n<li>Ensure effective set-up and ongoing management of studies within CTMS, eTMF, study finance systems and any other tools or local platforms required by country-specific laws and processes.</li>\n<li>Oversee, manage and coordinate all monitoring activities from site activation to closure according to Monitoring Plans, reviewing monitoring visit reports and providing guidance and support to monitors.</li>\n<li>Conduct co-monitoring visits, accompanied site visits and training visits with study CRAs to drive quality, consistency and development.</li>\n<li>Proactively identify risks, facilitate rapid resolution of complex study issues and escalate when necessary.</li>\n<li>Organize and lead regular, agenda-driven Local Study Team meetings that enable transparent communication, issue resolution and aligned decision-making.</li>\n<li>Build and maintain strong working relationships with Local Study Team members, site staff and global stakeholders to support smooth study execution.</li>\n<li>Report study progress, milestones, risks and mitigation plans to the Global Study Associate Director, Global Study Team and SMM/Study Operations Lead as applicable.</li>\n<li>Contribute to patient recruitment strategies and maintain regular contact with investigators to support enrolment targets.</li>\n<li>Develop, maintain and review a study-level country risk management plan, managing sites, stakeholders, vendors and customers to ensure timely risk identification and mitigation.</li>\n<li>Coordinate closely with National Coordinating Investigator or National Lead Investigator on recruitment and other key study matters where applicable.</li>\n<li>Plan and lead National Investigator Meetings in line with local codes when required.</li>\n<li>Support forecasting for study timelines, resource needs, recruitment, budgeting, materials and investigational product supply.</li>\n<li>Ensure set-up, updating and access to business-critical systems for Safety Reporting, Regulatory Submissions and Clinical Trial Transparency at country level.</li>\n<li>Ensure accuracy and compliance of all study payments in accordance with local regulations and agreements.</li>\n<li>Participate in training and coaching of new Local Study Team members to ensure quality delivery and adherence to ICH-GCP and AstraZeneca procedures.</li>\n<li>Maintain the study eTMF in an inspection-ready state at all times, ensuring documentation is complete, accurate and current.</li>\n<li>Plan and lead audit and regulatory inspection activities in collaboration with the Clinical Quality Associate Director and Quality Assurance teams.</li>\n<li>Contribute insights to process development and continuous improvement initiatives across the organization.</li>\n<li>Keep line managers regularly informed about study status, milestones, key issues and team performance.</li>\n<li>Ensure full compliance with local policies, codes of ethics and business practices in all study-related activities.</li>\n<li>Provide feedback on research trends, competing studies and site/investigator insights that can inform local strategy.</li>\n<li>Collaborate with the local Medical Affairs team as needed to support optimal study delivery and scientific quality.</li>\n<li>Actively support SMM initiatives at local, regional or global level as agreed with line management.</li>\n</ul>\n<p><strong>Essential Skills/Experience</strong></p>\n<ul>\n<li>Bachelor’s degree in related discipline with 5+ years of previous experience in the pharmaceutical industry</li>\n<li>Relevant knowledge and ability to fulfill key responsibilities, including but not limited to:</li>\n</ul>\n<p>+ Drug development process and related GxP processes, International guidelines ICH-GCP, relevant country regulations, medical knowledge and ability to learn relevant AZ Therapeutic Areas, Clinical Study Management including project management, monitoring, study drug handling and data management. \t+ Personal Effectiveness &amp; Drives Accountability in Others \t+ Learning Agility \t+ Financial, Technology &amp; Process Competency \t+ Active Listening, Fluency in written &amp; spoken business-level English \t+ Act with Integrity &amp; high ethical standards \t+ Effectively lead a team across in-person and virtual settings to deliver shared goals, demonstrates cultural awareness \t+ Identify and champion more efficient delivery of quality clinical trials with optimized cost and time \t+ Ability to travel nationally/internationally as required \t+ Valid driving license, if country employment requirement \t+ Communication &amp; Teamwork – Influencing, Collaboration, Impactful Site conversations \t+ Effective, risk-based thinking – Plans &amp; Aligns, Strategic thinking, Problem Solving, Critical Thinking, \t+ Decision Making, Effective Issue Management \t+ Clinical Study Operations (GCP) &amp; Quality Management – RbQM: Interpreting and implementing the Monitoring Plan, Study site selection &amp; set-up \t+ Deliver Priorities Results &amp; Impact – Project Management, Recruitment/Retention Planning &amp; Action</p>\n<p><strong>Desirable Skills/Experience</strong></p>\n<ul>\n<li>Bachelor&#39;s degree in the life sciences field is preferred</li>\n<li>Previous experience in Clinical Operations (CRA, SrCRA) or other related 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Effective, risk-based thinking, Plans & Aligns, Strategic thinking, Problem Solving, Critical Thinking, Decision Making, Effective Issue Management, Clinical Study Operations (GCP), Quality Management, RbQM, Interpreting and implementing the Monitoring Plan, Study site selection & set-up, Deliver Priorities Results & Impact, Recruitment/Retention Planning & Action, Bachelor's degree in the life sciences field, Previous experience in Clinical Operations (CRA, SrCRA), other related fields (Medical Affairs-led or Academic-led studies)"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_20647565-90a"},"title":"Associate Director, Process & Documentation","description":"<p>The Associate Director, Process &amp; Documentation for Data Management plays a key role in promoting and branding Data Management. Ensuring the efficiency of business operations and creating and implementing changes or improvements to process &amp; documentation, as needed.</p>\n<p>Plans and leads the strategy for process simplification and harmonization and ensures this is communicated across stakeholders and end users. The Associate Director, Process &amp; Documentation for Data Management plays a key role in providing functional process expertise, working closely with Subject Matter Experts within the functions and beyond, where required.</p>\n<p>Responsible for promoting and communicating activities in DM to stakeholders across the business and externally. Serves as the expert in Clinical Data Management Process development to provide oversight and advice to the SMEs regarding the CDM Governing documentation development and maintenance.</p>\n<p>Monitor regulatory, technical and pharma-industry trends to implement continuous process improvements. This position is responsible for one of the key components that supports Business Operations within Data Management and will collaborate with the other Associate Directors to strengthen the infrastructure of the function.</p>\n<p>Accountabilities:</p>\n<ul>\n<li>Accountable for the review and update of processes to ensure that DM deliverables can be met in a harmonized, simplified manner while remaining compliant with HA guidelines and ensuring quality and GxP compliance.</li>\n</ul>\n<ul>\n<li>Develops strategies for effectively communicating process changes internally and externally.</li>\n</ul>\n<ul>\n<li>Able to bring a six sigma approach to process to ensure best practices are being upheld.</li>\n</ul>\n<ul>\n<li>Evaluate and improve business processes. Brainstorm and collaborate with teams for new ideas to enhance processes.</li>\n</ul>\n<ul>\n<li>In close collaboration with Business Process Management, continue to monitor and assess processes to ensure they are producing the desired outcomes.</li>\n</ul>\n<ul>\n<li>Liaises with counterparts in Process and Enablement to ensure that company SOPs are updated as necessary.</li>\n</ul>\n<ul>\n<li>Develop and produce high-quality, informative, and interesting communications that brand DM.</li>\n</ul>\n<ul>\n<li>Ensure all messaging aligns with key business strategies.</li>\n</ul>\n<ul>\n<li>Develop content for social media, newsletters, town halls and any other distribution channels.</li>\n</ul>\n<ul>\n<li>Produces videos to detail who we are and what we do.</li>\n</ul>\n<ul>\n<li>Develop reports that showcase activities in Data Management.</li>\n</ul>\n<ul>\n<li>Develop questionnaires that allow us to get feedback from stakeholders and baseline our business.</li>\n</ul>\n<ul>\n<li>Collaborates closely with cross-functional colleagues (e.g. in SM&amp;M, Study Management, Programming) to understand and ensure connectivity and dependencies of DM processes on other functional processes are thoroughly considered when providing FPE input or working with PES to update processes.</li>\n</ul>\n<ul>\n<li>ECMS - Leads, facilitates, supports work in the tool.</li>\n</ul>\n<ul>\n<li>SOP steward and trainer, with functional SME support.</li>\n</ul>\n<ul>\n<li>Manages and coordinates the assignment of resources for the review cycles of Biometrics, Data Management and Clinical Operations owned governing documentation and determines the appropriate CDM SME involvement in the review of such documentation.</li>\n</ul>\n<p>Interacts with Learning, Standards &amp; Insights (LSI), Clinical Directors and CBDM Directors in this capacity.</p>\n<ul>\n<li>Represents and serves as the SME for Data Management during activities associated with all aspects of the LSI governing documentation system (AZDoc &amp; AZLearn).</li>\n</ul>\n<ul>\n<li>Partners with colleagues in LSI to ensure appropriate training curriculum is in place for DM staff.</li>\n</ul>\n<ul>\n<li>Translates business objectives into individual assignments and/or tasks.</li>\n</ul>\n<ul>\n<li>Collaborate and communicate with Biometrics, Data Management, Clinical Operations and partner CRO organizations to ensure coordination, compliance and proper use of DM Processes in data standards, database builds, programming and/or reports in clinical studies.</li>\n</ul>\n<ul>\n<li>Leads the creation of the workstreams for developing new CDM governing documentation and supporting documentation.</li>\n</ul>\n<ul>\n<li>Provides oversight and advice to the workstream regarding the activities of creating SOPs, Guidelines, Job Aids and supporting templates and forms.</li>\n</ul>\n<ul>\n<li>Provide expertise and consultancy to TA Leads on interpretation of CDM governing documentation to ensure overall CDM quality and consistency.</li>\n</ul>\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_20647565-90a","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Business Planning and Operations - Data Management","sameAs":"https://astrazeneca.eightfold.ai","logo":"https://logos.yubhub.co/astrazeneca.eightfold.ai.png"},"x-apply-url":"https://astrazeneca.eightfold.ai/careers/job/563877689867591","x-work-arrangement":"onsite","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":"$143,112.80 - $214,669.20","x-skills-required":["Clinical Data Management","Process Development","Documentation Management","Regulatory Compliance","Six Sigma","Communication","Leadership","Collaboration","Project Management","Data Standards","Database Builds","Programming","Reports","Training Curriculum","ECMS","SOP Stewardship","Resource Management","GxP Compliance"],"x-skills-preferred":[],"datePosted":"2026-04-24T14:14:10.441Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Durham, North Carolina, United States of America"}},"employmentType":"FULL_TIME","occupationalCategory":"Engineering","industry":"Healthcare","skills":"Clinical Data Management, Process Development, Documentation Management, Regulatory Compliance, Six Sigma, Communication, Leadership, Collaboration, Project Management, Data Standards, Database Builds, Programming, Reports, Training Curriculum, ECMS, SOP Stewardship, Resource Management, GxP Compliance","baseSalary":{"@type":"MonetaryAmount","currency":"USD","value":{"@type":"QuantitativeValue","minValue":143112.8,"maxValue":214669.2,"unitText":"YEAR"}}},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_e5385550-532"},"title":"Senior Scientist-Analytical Project Lead, Global Product Development","description":"<p>Are you ready to shape the future of medicines,pioneering technical and scientific breakthroughs that transform patient lives? We are seeking an experienced and innovative Analytical Project Lead based in Durham, North Carolina.</p>\n<p>Our vision is to transform product design, development, and characterization to enable delivery of new medicines to patients. In this role, you will lead analytical strategy and delivery for oral solid dosage (OSD) forms and, as needed, inhaled and/or parenteral products from early development through clinical supply and toward commercialization.</p>\n<p>As the analytical project/skill lead, you will partner across formulation, engineering, biopharmaceutics, manufacturing, QA and Regulatory to deliver robust methods, efficient control strategies, and submission-ready documentation. You will also help establish and optimize OSD laboratory capabilities at the Durham site, champion laboratory automation, and encourage adoption of modern data analytics and AI/ML tools to accelerate development and interpretation.</p>\n<p>We work, on average, a minimum of three days per week from the office. We balance the expectation of being in the office while respecting individual flexibility.</p>\n<p>Responsibilities include, but are not limited to:</p>\n<ul>\n<li>Project leadership: Act as analytical skill lead to secure major drug product deliveries, applying a risk-based, flexible approach to prioritization, resources, and timelines across modalities and dosage forms; integrate analytical plans with global teams and external partners/CMOs.</li>\n</ul>\n<ul>\n<li>Analytical strategy &amp; control: Define and own a phase-appropriate analytical control strategy aligned with CMC expectations across clinical phases; harmonize methods and embed lifecycle management to ensure robust, efficient control.</li>\n</ul>\n<ul>\n<li>Method development &amp; validation: Design, develop, validate, transfer, and lifecycle manage analytical methods for OSD (e.g., HPLC/UPLC, LC–MS, dissolution, impurity profiling, stability-indicating capability); establish scientifically supported system suitability, specifications, and fit-for-purpose sample preparation; ensure readiness for GMP execution with clear documentation and analyst guidance. Support inhaled and/or parenteral methods as needed.</li>\n</ul>\n<ul>\n<li>Characterization &amp; performance: Lead drug product characterization, comparability, and stability programs; direct forced degradation studies; for inhaled products where required, support aerodynamic performance assessments (e.g., impactor analysis).</li>\n</ul>\n<ul>\n<li>CMC &amp; regulatory: Author and review analytical CMC content for IND/IMPD/NDA/MAA; prepare validation reports, method transfer documents, and specifications; lead responses to regulatory queries and support shelf life assignment with appropriate statistics.</li>\n</ul>\n<ul>\n<li>Cross-functional collaboration: Work closely with formulators, engineers, supply and manufacturing sites, QA, Regulatory, and external partners/CMOs to integrate analytical deliverables into project plans and clinical manufacturing.</li>\n</ul>\n<ul>\n<li>Durham lab capability &amp; technology: Champion laboratory automation for sample preparation, method execution, and data analysis under GxP control.</li>\n</ul>\n<ul>\n<li>Problem-solving: Lead complex investigations, root cause analyses, and data integrity assessments; apply structured problem-solving (e.g., Six Sigma) and statistics to drive timely resolution and preventive actions.</li>\n</ul>\n<ul>\n<li>Digital, data &amp; innovation: Apply DoE and statistics for method robustness and understanding; use ELN/CDS and statistical tools; promote AI/ML, chemometrics, and predictive analytics to enhance interpretation, specification setting, and development speed; enable learning and standardization across projects; chip in to patenting and/or publishing.</li>\n</ul>\n<ul>\n<li>Quality &amp; governance: Ensure GxP compliance where applicable, data integrity, rigorous study design, and clear communication to governance bodies.</li>\n</ul>\n<p>Minimum Qualifications:</p>\n<ul>\n<li>Bachelor’s (12+ years), Master’s (6+ years), or PhD (or equivalent experience) in Analytical Chemistry, Pharmaceutical Sciences, Biochemistry, Biotechnology, or related field.</li>\n</ul>\n<ul>\n<li>Significant experience in pharmaceutical analytical science with current knowledge of regulatory CMC requirements for clinical and/or marketing applications.</li>\n</ul>\n<ul>\n<li>Demonstrated experience in analytical development for oral solid dosage forms; additional experience with inhaled and/or parenteral products preferred.</li>\n</ul>\n<ul>\n<li>Consistent record leading teams and/or scientific projects within a global organization and with external partners/CMOs; ability to influence cross-functional strategies.</li>\n</ul>\n<ul>\n<li>Strong proficiency with chromatographic techniques (HPLC/UPLC; LC–MS), dissolution, and complementary methodologies; for inhaled products, familiarity with aerosol performance characterization is a plus.</li>\n</ul>\n<ul>\n<li>Hands-on experience in method development (including use of supporting software), validation, transfer, and lifecycle management under ICH guidelines and phase-appropriate frameworks.</li>\n</ul>\n<ul>\n<li>Experience authoring analytical CMC content for submissions and responding to regulatory queries across clinical development.</li>\n</ul>\n<ul>\n<li>Experience working in a GMP/GxP environment; familiarity with instrument/equipment qualification, calibration, and maintenance expectations.</li>\n</ul>\n<ul>\n<li>Excellent communication, customer management, and influencing skills; ability to operate confidently and collaboratively across global, cross-disciplinary environments.</li>\n</ul>\n<ul>\n<li>Demonstrated ability to troubleshoot technical challenges and drive data-driven decisions.</li>\n</ul>\n<ul>\n<li>Fundamental digital and data capability relevant to analytical development, including:</li>\n</ul>\n<ul>\n<li>Proficiency with multivariate experimental design and basic DoE concepts for method and process understanding</li>\n</ul>\n<ul>\n<li>Working knowledge of statistics for analytical science (e.g., regression, ANOVA, capability/variation analysis, stability trending, OOS/OOT investigation)</li>\n</ul>\n<ul>\n<li>Practical use of ELN/CDS and statistical software (e.g., JMP or Minitab) for data analysis and reporting</li>\n</ul>\n<p>Preferred Qualifications:</p>\n<ul>\n<li>Strategic chromatographic and separation science leadership: define orthogonal method suites (e.g., RP, HILIC, ion exchange, SEC, SFC, CE) to secure impurity resolution and stability-indicating capability; apply LC–MS(/MS) for structure confirmation and quantitation; use multidimensional LC and targeted DoE to accelerate development and set robust specifications; harmonize methods across sites with clear comparability criteria; embed lifecycle management and coach teams through complex separations (e.g., peptides, oligonucleotides, challenging matrices).</li>\n</ul>\n<ul>\n<li>OSD focus: Support with establishing, equipping, and optimizing OSD test equipment and processes at the Durham site.</li>\n</ul>\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_e5385550-532","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Analytical Development","sameAs":"https://astrazeneca.eightfold.ai","logo":"https://logos.yubhub.co/astrazeneca.eightfold.ai.png"},"x-apply-url":"https://astrazeneca.eightfold.ai/careers/job/563877689929250","x-work-arrangement":"hybrid","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["Analytical Chemistry","Pharmaceutical Sciences","Biochemistry","Biotechnology","Chromatographic techniques","Dissolution","LC–MS","HPLC/UPLC","Method development","Validation","Transfer","Lifecycle management","ICH guidelines","Phase-appropriate frameworks","Analytical CMC content","Regulatory queries","GMP/GxP environment","Instrument/equipment qualification","Calibration","Maintenance","Experimental design","Statistics","ELN/CDS","Statistical software","Data analysis","Reporting"],"x-skills-preferred":["Strategic chromatographic and separation science leadership","Orthogonal method suites","LC–MS(/MS)","Multidimensional LC","Targeted DoE","Robust specifications","Harmonized methods","Complex separations","Peptides","Oligonucleotides","Challenging matrices","OSD focus","Establishing","Equipping","Optimizing","Test equipment","Processes"],"datePosted":"2026-04-24T14:13:54.042Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Durham, North Carolina, United States of America"}},"employmentType":"FULL_TIME","occupationalCategory":"Engineering","industry":"Healthcare","skills":"Analytical Chemistry, Pharmaceutical Sciences, Biochemistry, Biotechnology, Chromatographic techniques, Dissolution, LC–MS, HPLC/UPLC, Method development, Validation, Transfer, Lifecycle management, ICH guidelines, Phase-appropriate frameworks, Analytical CMC content, Regulatory queries, GMP/GxP environment, Instrument/equipment qualification, Calibration, Maintenance, Experimental design, Statistics, ELN/CDS, Statistical software, Data analysis, Reporting, Strategic chromatographic and separation science leadership, Orthogonal method suites, LC–MS(/MS), Multidimensional LC, Targeted DoE, Robust specifications, Harmonized methods, Complex separations, Peptides, Oligonucleotides, Challenging matrices, OSD focus, Establishing, Equipping, Optimizing, Test equipment, Processes"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_363bbf83-482"},"title":"Manager, AI Deployment Engineering - Health & Life Sciences","description":"<p><strong>Compensation</strong></p>\n<ul>\n<li>Zone A$251K – $335K • Offers Equity</li>\n</ul>\n<p>The base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. If the role is non-exempt, overtime pay will be provided consistent with applicable laws. In addition to the salary range listed above, total compensation also includes generous equity, performance-related bonus(es) for eligible employees, and the following benefits.</p>\n<ul>\n<li>Medical, dental, and vision insurance for you and your family, with employer contributions to Health Savings Accounts</li>\n</ul>\n<ul>\n<li>Pre-tax accounts for Health FSA, Dependent Care FSA, and commuter expenses (parking and transit)</li>\n</ul>\n<ul>\n<li>401(k) retirement plan with employer match</li>\n</ul>\n<ul>\n<li>Paid parental leave (up to 24 weeks for birth parents and 20 weeks for non-birthing parents), plus paid medical and caregiver leave (up to 8 weeks)</li>\n</ul>\n<ul>\n<li>Paid time off: flexible PTO for exempt employees and up to 15 days annually for non-exempt employees</li>\n</ul>\n<ul>\n<li>13+ paid company holidays, and multiple paid coordinated company office closures throughout the year for focus and recharge, plus paid sick or safe time (1 hour per 30 hours worked, or more, as required by applicable state or local law)</li>\n</ul>\n<ul>\n<li>Mental health and wellness support</li>\n</ul>\n<ul>\n<li>Employer-paid basic life and disability coverage</li>\n</ul>\n<ul>\n<li>Annual learning and development stipend to fuel your professional growth</li>\n</ul>\n<ul>\n<li>Daily meals in our offices, and meal delivery credits as eligible</li>\n</ul>\n<ul>\n<li>Relocation support for eligible employees</li>\n</ul>\n<ul>\n<li>Additional taxable fringe benefits, such as charitable donation matching and wellness stipends, may also be provided.</li>\n</ul>\n<p><strong>About the Team</strong></p>\n<p>The AI Deployment Engineering team works at the intersection of cutting-edge AI research and real-world application. We partner directly with OpenAI’s most strategic customers to design, implement, and scale production deployments of generative AI systems. Our work ensures that organizations can safely and effectively integrate AI into critical workflows.</p>\n<p>Within this team, the Health &amp; Life Sciences (HLS) segment focuses on enabling pharmaceutical manufacturers, biotechnology companies, medical device organizations, contract research organizations (CROs), and health systems to adopt AI responsibly in regulated environments. We work across clinical, scientific, regulatory, and operational functions to unlock meaningful impact while maintaining the highest standards of safety, privacy, and compliance.</p>\n<p><strong>About the Role</strong></p>\n<p>We are seeking a Manager, AI Deployment Engineering to lead our Healthcare &amp; Life Sciences deployment efforts. In this role, you will build and mentor a high-performing team of deployment engineers dedicated to helping HLS organizations move from experimentation to production with OpenAI technologies.</p>\n<p>You will operate at both strategic and technical levels , partnering with executive stakeholders, technical leaders, and cross-functional internal teams to deliver secure, compliant, and high-impact AI deployments. This role requires a strong technical foundation, people leadership experience, and a deep appreciation for the complexity of regulated healthcare and life sciences environments.</p>\n<p>This role is based in San Francisco or Seattle. 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We push the boundaries of the capabilities of AI systems and seek to safely deploy them to the world through our products. AI is an extremely powerful tool that must be created with safety and human needs at its core, and to achieve our mission, we must encompass and value the many different perspectives, voices, and experiences that form the full spectrum of humanity.</p>\n<p>We are an equal opportunity employer, and we do not discriminate on the basis of race, religion, color, national origin, sex, sexual orientation, age, veteran status, disability, genetic information, or other applicable legally protected characteristic.</p>\n<p>For additional information, please see [OpenAI’s Affirmative Action and Equal Employment Opportunity Policy Statement](https://cdn.openai.com/policies/eeo-policy-statement.pdf).</p>\n<p>Background checks for applicants will be administered in accordance with applicable law, and qualified applicants with arrest or conviction records will be considered for employment consistent with those laws, including the San Francisco Fair Chance Ordinance, the Los Angeles County Fair Chance Ordinance for Employers, and the California Fair Chance Act, for US-based candidates. For unincorporated Los Angeles County workers: we reasonably believe that criminal history may have a direct, adverse and negative relationship with the following job duties, potentially resulting in the withdrawal of a conditional offer of employment: protect computer hardware entrusted to you from theft, loss or damage; return all computer hardware in your possession (including the data contained therein) upon termination of employment or end of assignment; and maintain the confidentiality of proprietary, confidential, and non-public information. 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We are the critical link that brings innovation from our science labs to patients around the world.</p>\n<p>We&#39;re achieving all of this while continuing to accelerate our operational excellence through innovative science, Lean ways of working, and evolving digital technologies.</p>\n<p>Using cell therapy to halt and reverse disease, restore damaged organs, and, ultimately, cure many life-threatening conditions is now a realistic goal for our scientists and operators.</p>\n<p>About Rockville Manufacturing Centre (RMC):</p>\n<p>Our role in Operations is to bring these promising therapies from the lab to life through a thorough process of development, manufacturing, testing and supply.</p>\n<p>Our fast-paced, growing environment provides a wealth of opportunity and global opportunities to learn from other teams, embrace lifelong learning and build capabilities, setting your own direction and pace for your long-term career.</p>\n<p>Introduction to role:</p>\n<p>Are you ready to develop an attitude of excellence? Join AstraZeneca&#39;s Operations team as the Quality Systems &amp; Compliance Associate Director, Cell Therapy at the Rockville Manufacturing Centre (RMC) facility, the newest addition to our global supply network.</p>\n<p>We aim to make a direct impact on patients by delivering life-saving cell therapies. This is your chance to break new ground and leave a collective legacy!</p>\n<p>Accountabilities:</p>\n<p>As the Quality Systems &amp; Compliance Associate Director, Cell Therapy, you will provide leadership, direction and mentoring to ensure that the QS/C organisation is successful in meeting the quality and manufacturing objectives in support of site goals.</p>\n<p>You will represent the QS/C department and/or the Quality Organisation on assigned site governance and operational teams internally, and as an empowered functional representative externally to ensure results are aligned with site business objectives.</p>\n<p>You will facilitate the growth and development of QS/C staff, provide strategic support to the Quality Site Lead, Compliance and Site Support, for operational and long-term growth, and demonstrate excellent communication skills through internal and external channels.</p>\n<p>Essential Skills/Experience:</p>\n<ul>\n<li>B.S. degree in Science, Engineering, Pharmacy, or related technical field with a minimum of 5 years of applicable experience</li>\n</ul>\n<ul>\n<li>Minimum of 2 years of management/supervisory/project management experience</li>\n</ul>\n<ul>\n<li>Experience in audit and inspection management</li>\n</ul>\n<ul>\n<li>Consistent record of working in a fast-paced, cross-functional work environment</li>\n</ul>\n<ul>\n<li>Excellent written and verbal communication skills</li>\n</ul>\n<ul>\n<li>Team oriented approach to project management and problem resolution</li>\n</ul>\n<ul>\n<li>Proven record of making decisions that balance patient safety, compliance, and supply</li>\n</ul>\n<ul>\n<li>Ability to influence senior collaborators, both internally and externally</li>\n</ul>\n<ul>\n<li>Ability to multi-task and prioritise work</li>\n</ul>\n<p>Desirable Skills/Experience:</p>\n<ul>\n<li>M.S. degree in Science, Engineering, Pharmacy, or related technical field with a minimum of 5 years of applicable experience</li>\n</ul>\n<ul>\n<li>Advanced degree in Science, Engineering, Biochemistry, Pharmacy or related technical field</li>\n</ul>\n<ul>\n<li>Experience with Quality Systems (e.g. Veeva Vault) is desirable.</li>\n</ul>\n<ul>\n<li>Experience with Cell Therapy regulatory inspections</li>\n</ul>\n<ul>\n<li>Extensive working knowledge of international Cell Therapy GxP regulatory frameworks, regulations, and guidance.</li>\n</ul>\n<ul>\n<li>Experience engaging with global regulatory bodies</li>\n</ul>\n<ul>\n<li>Consistent track record of attracting and developing talent</li>\n</ul>\n<p>Benefits:</p>\n<p>AstraZeneca offers a competitive salary range of $129,556.80 - $194,335.20 USD Annual, a short-term incentive bonus opportunity, eligibility to participate in our equity-based long-term incentive program (salaried roles), to receive a retirement contribution (hourly roles), and commission payment eligibility (sales roles).</p>\n<p>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.</p>\n<p>Additional details of participation in these benefit plans will be provided if an employee receives an offer of employment.</p>\n<p>If hired, employee will be in an &#39;at-will position&#39; and the Company reserves the right to modify base pay (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors.</p>\n<p>At AstraZeneca, we champion a perspective of excellence. Our environment is driven by a belief that good can always be better. We continuously seek opportunities to contribute by harnessing science and evidence to foresee risks. It&#39;s a place where innovation thrives as we focus on delivering life-changing medicines to patients.</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_904b9845-2ff","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Quality Cell Therapy","sameAs":"https://astrazeneca.eightfold.ai","logo":"https://logos.yubhub.co/astrazeneca.eightfold.ai.png"},"x-apply-url":"https://astrazeneca.eightfold.ai/careers/job/563877689842338","x-work-arrangement":"hybrid","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":"$129,556.80 - $194,335.20 USD Annual","x-skills-required":["B.S. degree in Science, Engineering, Pharmacy, or related technical field","Minimum of 5 years of applicable experience","Minimum of 2 years of management/supervisory/project management experience","Experience in audit and inspection management","Consistent record of working in a fast-paced, cross-functional work environment"],"x-skills-preferred":["M.S. degree in Science, Engineering, Pharmacy, or related technical field","Advanced degree in Science, Engineering, Biochemistry, Pharmacy or related technical field","Experience with Quality Systems (e.g. Veeva Vault)","Experience with Cell Therapy regulatory inspections","Extensive working knowledge of international Cell Therapy GxP regulatory frameworks, regulations, and guidance."],"datePosted":"2026-04-18T22:16:07.152Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Rockville, Maryland, United States of America"}},"employmentType":"FULL_TIME","occupationalCategory":"Engineering","industry":"Biotechnology","skills":"B.S. degree in Science, Engineering, Pharmacy, or related technical field, Minimum of 5 years of applicable experience, Minimum of 2 years of management/supervisory/project management experience, Experience in audit and inspection management, Consistent record of working in a fast-paced, cross-functional work environment, M.S. degree in Science, Engineering, Pharmacy, or related technical field, Advanced degree in Science, Engineering, Biochemistry, Pharmacy or related technical field, Experience with Quality Systems (e.g. Veeva Vault), Experience with Cell Therapy regulatory inspections, Extensive working knowledge of international Cell Therapy GxP regulatory frameworks, regulations, and guidance.","baseSalary":{"@type":"MonetaryAmount","currency":"USD","value":{"@type":"QuantitativeValue","minValue":129556.8,"maxValue":194335.2,"unitText":"YEAR"}}},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_939bf63c-00b"},"title":"Specialist, Global Clinical Solutions (IRT Lead)","description":"<p>Role Details</p>\n<p>The Specialist, Global Clinical Solutions (IRT Lead) provides global centralized services across drug projects and related activities, helping clinical development programs meet time, cost, and quality expectations across all delivery models.</p>\n<p>Key Responsibilities</p>\n<ul>\n<li>Deliver GCS services that support clinical development activities across multiple projects and stakeholders.</li>\n<li>Set up and maintain systems, tools, and data associated with projects, services, and technology in partnership with Study Teams and external partners, ensuring appropriate standards, completeness, quality, and consistency.</li>\n<li>Support life cycle management and business continuity for operational processes, procedures, systems, tools, standards, procedural documentation, and training materials.</li>\n<li>Provide support to user communities by conducting relevant process, system, and tool trainings, facilitating knowledge sharing, establishing best practice, and maintaining effective communication with stakeholders across GCS and AstraZeneca.</li>\n<li>Perform analyses of processes and tools to define business usage and identify opportunities to improve efficiency and effectiveness of systems, methods, and processes; support the development of User Requirement Specifications and User Acceptance Tests.</li>\n<li>Contribute to business cases for continuous improvement projects that enhance how we deliver clinical studies.</li>\n<li>Prioritize workload effectively to achieve personal and work unit targets in a dynamic environment.</li>\n<li>Participate in change initiatives that evolve our ways of working and enable better outcomes for patients.</li>\n</ul>\n<p>Essential Skills and Experience</p>\n<ul>\n<li>Bachelor&#39;s degree with 0+ years of work experience in the pharmaceutical industry or in clinical study delivery/clinical development processes.</li>\n<li>Proven organizational and analytical skills, as well as proven ability to multitask.</li>\n<li>Strong time management skills and task-oriented performance.</li>\n<li>Previous administrative training/experience.</li>\n<li>Computer proficiency.</li>\n<li>Excellent knowledge of spoken and written English.</li>\n<li>Strong communication skills.</li>\n</ul>\n<p>Desirable Skills and Experience</p>\n<ul>\n<li>A good understanding of the clinical study process.</li>\n<li>Programming experience or programming aptitude.</li>\n<li>Knowledge of pharmaceutical drug development and clinical study processes and associated government regulations, ICH GCP.</li>\n<li>Shown willingness and ability to train others on study support processes and procedures.</li>\n<li>Demonstrate the ability to proactively identify risks and issues as well as possible solutions.</li>\n<li>GxP trained.</li>\n</ul>\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_939bf63c-00b","directApply":true,"hiringOrganization":{"@type":"Organization","name":"GCS Services","sameAs":"https://astrazeneca.eightfold.ai","logo":"https://logos.yubhub.co/astrazeneca.eightfold.ai.png"},"x-apply-url":"https://astrazeneca.eightfold.ai/careers/job/563877689867686","x-work-arrangement":"hybrid","x-experience-level":"entry","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["Bachelor's degree","Pharmaceutical industry experience","Clinical study delivery/clinical development processes experience","Organizational and analytical skills","Multitasking ability","Time management skills","Administrative training/experience","Computer proficiency","Excellent knowledge of spoken and written English","Strong communication skills"],"x-skills-preferred":["Good understanding of clinical study process","Programming experience or programming aptitude","Knowledge of pharmaceutical drug development and clinical study processes and associated government regulations, ICH GCP","Ability to train others on study support processes and procedures","Ability to proactively identify risks and issues as well as possible solutions","GxP trained"],"datePosted":"2026-04-18T22:13:39.220Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Durham, North Carolina, United States of America"}},"employmentType":"FULL_TIME","occupationalCategory":"Engineering","industry":"Healthcare","skills":"Bachelor's degree, Pharmaceutical industry experience, Clinical study delivery/clinical development processes experience, Organizational and analytical skills, Multitasking ability, Time management skills, Administrative training/experience, Computer proficiency, Excellent knowledge of spoken and written English, Strong communication skills, Good understanding of clinical study process, Programming experience or programming aptitude, Knowledge of pharmaceutical drug development and clinical study processes and associated government regulations, ICH GCP, Ability to train others on study support processes and procedures, Ability to proactively identify risks and issues as well as possible solutions, GxP trained"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_f59c4a7f-68e"},"title":"Test Engineering Leader - Evinova","description":"<p>Join Evinova, a health-tech business, in accelerating better health outcomes by advancing digital transformation across the life sciences sector. We&#39;re building AI-native products that reshape how clinical trials are designed, documented, and delivered. 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You will partner with Research, Product, Policy, Security Team, and Frontier Red Team to ensure cybersecurity safety is embedded throughout the model development lifecycle.</p>\n<p>You will translate cybersecurity domain knowledge into actionable safety requirements and clearly articulated policies. You will contribute to external communications, including model cards, blog posts, and policy documents related to cybersecurity safety.</p>\n<p>You will monitor emerging technologies and threat landscapes for their potential to contribute to new risks and mitigation strategies, and strategically address these.</p>\n<p>You will mentor and develop team members, fostering a culture of technical excellence and responsible AI development.</p>\n<p>To be successful in this role, you will need to have:</p>\n<ul>\n<li>An M.S. or PhD in Computer Science, Cybersecurity, or a related technical field, OR equivalent professional experience in offensive or defensive cybersecurity</li>\n<li>5+ years of hands-on experience in cybersecurity, with deep expertise in areas such as vulnerability research, exploit development, network security, malware analysis, or penetration testing</li>\n<li>2+ years of experience managing technical teams or leading complex technical projects with multiple stakeholders</li>\n<li>Experience in scientific computing and data analysis, with proficiency in programming (Python preferred)</li>\n<li>Deep expertise in modern cybersecurity, including both offensive techniques (vulnerability research, exploit development, penetration testing, malware analysis) and defensive measures (detection, monitoring, incident response)</li>\n<li>Demonstrated ability to create threat models and translate technical cyber risks into policy frameworks</li>\n<li>Familiarity with responsible disclosure practices, vulnerability coordination, and cybersecurity frameworks (e.g., MITRE ATT&amp;CK, NIST Cybersecurity Framework, CWE/CVE systems)</li>\n<li>Strong analytical and writing skills, with the ability to navigate ambiguity and explain complex technical concepts to non-technical stakeholders</li>\n<li>Experience developing policies or guidelines at scale, balancing safety concerns with enabling legitimate use cases</li>\n<li>A passion for learning new skills and an ability to rapidly adapt to changing techniques and technologies</li>\n<li>Comfort working in a fast-paced environment where priorities may shift as AI capabilities evolve</li>\n<li>Track record of translating specialized technical knowledge into actionable safety policies or enforcement guidelines</li>\n</ul>\n<p>Preferred qualifications include:</p>\n<ul>\n<li>Background in AI/ML systems, particularly experience with large language models</li>\n<li>Experience developing ML-based security systems or adversarial ML research</li>\n<li>Experience working with defense, intelligence, or security organizations (e.g., NSA, CISA, national labs, security contractors)</li>\n<li>Published security research, disclosed vulnerabilities, or participated in bug bounty programs</li>\n<li>Understanding of Trust &amp; Safety operations and content moderation at scale</li>\n<li>Certifications such as OSCP, OSCE, GXPN, or equivalent demonstrating technical depth</li>\n<li>Understanding of dual-use security research concerns and ethical considerations in AI safety</li>\n</ul>\n<p>The annual compensation range for this role is $320,000-$405,000 USD.</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_7cc85573-4a2","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Anthropic","sameAs":"https://www.anthropic.co/","logo":"https://logos.yubhub.co/anthropic.co.png"},"x-apply-url":"https://job-boards.greenhouse.io/anthropic/jobs/5066981008","x-work-arrangement":"hybrid","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":"$320,000-$405,000 USD","x-skills-required":["Cybersecurity","Vulnerability research","Exploit development","Network security","Malware analysis","Penetration testing","Detection","Monitoring","Incident response","Scientific computing","Data analysis","Programming (Python)","Responsible disclosure practices","Vulnerability coordination","Cybersecurity frameworks (MITRE ATT&CK, NIST Cybersecurity Framework, CWE/CVE systems)"],"x-skills-preferred":["AI/ML systems","Large language models","ML-based security systems","Adversarial ML research","Defense, intelligence, or security organizations","Published security research","Disclosed vulnerabilities","Bug bounty programs","Trust & Safety operations","Content moderation at scale","Certifications (OSCP, OSCE, GXPN)"],"datePosted":"2026-04-18T15:56:47.739Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Remote-Friendly (Travel-Required) | San Francisco, CA | Washington, DC"}},"jobLocationType":"TELECOMMUTE","employmentType":"FULL_TIME","occupationalCategory":"Engineering","industry":"Technology","skills":"Cybersecurity, Vulnerability research, Exploit development, Network security, Malware analysis, Penetration testing, Detection, Monitoring, Incident response, Scientific computing, Data analysis, Programming (Python), Responsible disclosure practices, Vulnerability coordination, Cybersecurity frameworks (MITRE ATT&CK, NIST Cybersecurity Framework, CWE/CVE systems), AI/ML systems, Large language models, ML-based security systems, Adversarial ML research, Defense, intelligence, or security organizations, Published security research, Disclosed vulnerabilities, Bug bounty programs, Trust & Safety operations, Content moderation at scale, Certifications (OSCP, OSCE, GXPN)","baseSalary":{"@type":"MonetaryAmount","currency":"USD","value":{"@type":"QuantitativeValue","minValue":320000,"maxValue":405000,"unitText":"YEAR"}}},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_c76d0c6d-ec7"},"title":"Technical Policy Manager, Cyber Harms","description":"<p><strong>About the Role:</strong></p>\n<p>We are looking for a cybersecurity expert to lead our efforts to prevent AI misuse in the cyber domain. As a Cyber Harms Technical Policy Manager, you will lead a team applying deep technical expertise to inform the design of safety systems that detect harmful cyber behaviours and prevent misuse by sophisticated threat actors.</p>\n<p><strong>In this role, you will:</strong></p>\n<ul>\n<li>Lead and grow a team of technical specialists focused on cyber threat modelling and evaluation frameworks</li>\n<li>Design and oversee execution of capability evaluations (&#39;evals&#39;) to assess the cyber-relevant capabilities of new models</li>\n<li>Create comprehensive cyber threat models, including attack vectors, exploit chains, precursor identification, and weaponization techniques</li>\n<li>Develop and iterate on usage policies that govern responsible use of our models for emerging capabilities and use cases related to cyber harms</li>\n<li>Serve as the primary domain expert on cyber harms, advising cross-functional teams on threat landscapes and mitigation strategies</li>\n<li>Collaborate closely with internal and external threat modelling experts to develop training data for safety systems, and with ML engineers to train these systems, optimising for both robustness against adversarial attacks and low false-positive rates for legitimate security researchers</li>\n<li>Analyse safety system performance in traffic, identifying gaps and proposing improvements</li>\n<li>Conduct regular reviews of existing policies and enforcement systems to identify and address gaps and ambiguities related to cybersecurity risks</li>\n<li>Develop rigorous stress-testing of safeguards against evolving cyber threats and product surfaces</li>\n<li>Partner with Research, Product, Policy, Security Team, and Frontier Red Team to ensure cybersecurity safety is embedded throughout the model development lifecycle</li>\n<li>Translate cybersecurity domain knowledge into actionable safety requirements and clearly articulated policies</li>\n<li>Contribute to external communications, including model cards, blog posts, and policy documents related to cybersecurity safety</li>\n<li>Monitor emerging technologies and threat landscapes for their potential to contribute to new risks and mitigation strategies, and strategically address these</li>\n<li>Mentor and develop team members, fostering a culture of technical excellence and responsible AI development</li>\n</ul>\n<p><strong>You may be a good fit if you have:</strong></p>\n<ul>\n<li>An M.S. or PhD in Computer Science, Cybersecurity, or a related technical field, OR equivalent professional experience in offensive or defensive cybersecurity</li>\n<li>5+ years of hands-on experience in cybersecurity, with deep expertise in areas such as vulnerability research, exploit development, network security, malware analysis, or penetration testing</li>\n<li>2+ years of experience managing technical teams or leading complex technical projects with multiple stakeholders</li>\n<li>Experience in scientific computing and data analysis, with proficiency in programming (Python preferred)</li>\n<li>Deep expertise in modern cybersecurity, including both offensive techniques (vulnerability research, exploit development, penetration testing, malware analysis) and defensive measures (detection, monitoring, incident response)</li>\n<li>Demonstrated ability to create threat models and translate technical cyber risks into policy frameworks</li>\n<li>Familiarity with responsible disclosure practices, vulnerability coordination, and cybersecurity frameworks (e.g., MITRE ATT&amp;CK, NIST Cybersecurity Framework, CWE/CVE systems)</li>\n<li>Strong analytical and writing skills, with the ability to navigate ambiguity and explain complex technical concepts to non-technical stakeholders</li>\n<li>Experience developing policies or guidelines at scale, balancing safety concerns with enabling legitimate use cases</li>\n<li>A passion for learning new skills and an ability to rapidly adapt to changing techniques and technologies</li>\n<li>Comfort working in a fast-paced environment where priorities may shift as AI capabilities evolve</li>\n<li>Track record of translating specialised technical knowledge into actionable safety policies or enforcement guidelines</li>\n</ul>\n<p><strong>Preferred Qualifications:</strong></p>\n<ul>\n<li>Background in AI/ML systems, particularly experience with large language models</li>\n<li>Experience developing ML-based security systems or adversarial ML research</li>\n<li>Experience working with defence, intelligence, or security organisations (e.g., NSA, CISA, national labs, security contractors)</li>\n<li>Published security research, disclosed vulnerabilities, or participated in bug bounty programs</li>\n<li>Understanding of Trust &amp; Safety operations and content moderation at scale</li>\n<li>Certifications such as OSCP, OSCE, GXPN, or equivalent demonstrating technical depth</li>\n<li>Understanding of dual-use security research concerns and ethical considerations in AI safety</li>\n</ul>\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_c76d0c6d-ec7","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Anthropic","sameAs":"https://job-boards.greenhouse.io","logo":"https://logos.yubhub.co/anthropic.com.png"},"x-apply-url":"https://job-boards.greenhouse.io/anthropic/jobs/5066981008","x-work-arrangement":"remote","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":"The annual compensation for this role is not specified in the job posting.","x-skills-required":["cybersecurity","vulnerability research","exploit development","network security","malware analysis","penetration testing","scientific computing","data analysis","programming (Python)","threat modelling","policy frameworks","responsible disclosure practices","vulnerability coordination","cybersecurity frameworks (e.g., MITRE ATT&CK, NIST Cybersecurity Framework, CWE/CVE systems)"],"x-skills-preferred":["AI/ML systems","large language models","ML-based security systems","adversarial ML research","defence, intelligence, or security organisations","NSA, CISA, national labs, security contractors","published security research","disclosed vulnerabilities","bug bounty programs","Trust & Safety operations","content moderation at scale","OSCP, OSCE, GXPN, or equivalent certifications","dual-use security research concerns","ethical considerations in AI safety"],"datePosted":"2026-03-08T13:50:25.823Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"San Francisco, CA, Washington, DC"}},"jobLocationType":"TELECOMMUTE","employmentType":"FULL_TIME","occupationalCategory":"Engineering","industry":"Technology","skills":"cybersecurity, vulnerability research, exploit development, network security, malware analysis, penetration testing, scientific computing, data analysis, programming (Python), threat modelling, policy frameworks, responsible disclosure practices, vulnerability coordination, cybersecurity frameworks (e.g., MITRE ATT&CK, NIST Cybersecurity Framework, CWE/CVE systems), AI/ML systems, large language models, ML-based security systems, adversarial ML research, defence, intelligence, or security organisations, NSA, CISA, national labs, security contractors, published security research, disclosed vulnerabilities, bug bounty programs, Trust & Safety operations, content moderation at scale, OSCP, OSCE, GXPN, or equivalent certifications, dual-use security research concerns, ethical considerations in AI safety"}]}