Humanity Protocol jobs

Research Audiologist Montgomery County, Maryland Summary This position is located within the Auditory and Vestibular Clinical Research Section (AVCRS), Neurotology Branch (NB), National Institute on Deafness and Other Communication Disorders (NIDCD), National Institutes of Health (NIH). The incumbent engages in clinical research on mechanisms of auditory and vestibular function/dysfunction, rare disease, and earliest detection in humans across the lifespan. Duties Conduct research of the auditory and vestibular systems. Serve as the lead/primary investigator for several assigned areas of investigation for which she/he is the subject matter expert, and as a project member for most of the research projects conducted in the AVCRS. Evaluate auditory and vestibular function of subjects participating in AVCRS research protocols, and of patients participating in other research protocols at the NIH Clinical Center. Modify parameters to achieve customized assessments and to evaluate feasibility and superiority of various techniques. Responsible for the management of laboratory equipment, computers and software, and oversight of equipment calibration. Evaluate new instrumentation and makes recommendations concerning the purchase of new scientific instruments and computers and software. Develop novel approaches and methodologies for assessment and documentation of functional aspects of the auditory and vestibular systems. Assist the Chief Research Audiologist by facilitating the efficient and productive operation of the lab. Education This position has an education requirement. You are strongly encouraged to submit a copy of your transcripts (or a list of your courses including titles, credit hours completed and grades). Unofficial transcripts will be accepted in the application package. Official transcripts will

Preclinical Study Coordinator Austin, Texas, United States About Neuralink: We are creating devices that enable a bi-directional interface with the brain. These devices allow us to restore movement to the paralyzed, restore sight to the blind, and revolutionize how humans interact with their digital world. Team Description: The Preclinical Team is responsible for designing, conducting, documenting, analyzing, and reporting preclinical studies. Our team provides a means for ensuring the safe, effective, and robust implantation of Neuralink devices into animals and, ultimately, humans. Job Description and Responsibilities: The Study Coordinator provides critical operational and project management support to the Study Director in GLP-regulated preclinical studies for Neuralink devices. This role handles the majority of day-to-day coordination, scheduling, data compilation, and administrative tasks, enabling the Study Director to focus on scientific oversight, data interpretation, and regulatory compliance. The Study Coordinator acts as a key liaison across the preclinical team, technical staff, and cross-functional groups to ensure studies progress smoothly, on time, and in compliance with protocols and SOPs. The Study Coordinator will: - Support the Study Director in developing study protocols, amendments, and related documentation. - Facilitate cross-functional communication, establish and track study timelines, and prepare/lead study milestone meetings. - Identify and help eliminate roadblocks that could delay study progress. - Assist with implementation of test methods and practices described in the study protocol and SOPs. - Help ensure all experimental data, including observations of unanticipated responses of the test system, are accurately recorded and verified. - Manage the study schedule, alerting

Senior Product Designer New York, United States Uniswap Labs is a core contributor to the Uniswap Protocol, the world's largest DEX, with over $4 trillion in volume across 17 chains. It builds products that help millions access the protocol, including the Uniswap Web App, Wallet, and Trading API. Uniswap Labs is also the primary technical provider for Unichain, a DeFi-native Ethereum Layer 2 built to be the home for liquidity across chains. When you join Uniswap Labs, you become part of a team that's reshaping the way value flows on the internet. We're looking for an enthusiastic, self-motivated designer to help us build the next generation of financial products. You'll be joining a small but close knit product team known for developing category-defining UX. As a Senior Product Designer at Uniswap Labs, you'll solve cutting edge human computer or mobile interface problems as well as develop new mental models for the next million users of decentralized finance. We are headquartered in SoHo in New York City. This role will be based in our office with an expectation of regular in-person collaboration. Responsibilities: - Own and deliver end-to-end design projects for new and improved consumer products that increase clarity and user agency in decentralized finance and web3 - Tackle complex challenges in emerging technology by inventing new mental models and designing cutting-edge interactions with minimal oversight - Use a human-centered approach that incorporates qualitative and quantitative data to create conceptual wireframes, prototypes, and high-fidelity designs. - Effectively collaborate cross-functionally with engineering,

Field Clinical Engineer South San Francisco, California, United States About Neuralink: We are creating devices that enable a bi-directional interface with the brain. These devices allow us to restore movement to the paralyzed, restore sight to the blind, and revolutionize how humans interact with their digital world. Team Description: The Neuralink Clinical team is at the heart of an ecosystem that merges neuroscience, engineering, and medicine. We work to shape the future of brain-computer interface (BCI) technology through the planning, launch, and execution of groundbreaking human clinical trials. Our team is built on a foundation of excellence, aiming to uphold the highest standards of Good Clinical Practice (GCP) while redefining what's possible and revolutionizing the way people interact with technology. Through strict compliance with ethical and regulatory protocols, we focus on ensuring the well-being of our trial participants while advancing the frontiers of neuroscience! Every day will bring fresh challenges and unprecedented opportunities to pioneer new approaches in the pursuit of our mission. From navigating regulatory pathways, designing trial protocols and documentation, and executing clinical trials, our team is instrumental in translating Neuralink's BCI technology for use in people! Job Description and Responsibilities: As a Field Clinical Engineer, you will be on the front lines of Neuralink's clinical programs, working directly with participants, clinicians, and internal teams to translate cutting-edge neurotechnology into meaningful functional outcomes. This role is ideal for individuals with a background in PM&R, occupational therapy, or physical therapy who also have experience in medical devices and thrive

Materials R&D Technician, Silicon Crystal Growth Bastrop, TX SpaceX was founded under the belief that a future where humanity is out exploring the stars is fundamentally more exciting than one where we are not. Today SpaceX is actively developing the technologies to make this possible, with the ultimate goal of enabling human life on Mars. MATERIALS R&D TECHNICIAN, SILICON CRYSTAL GROWTH As a Materials R&D Technician, Silicon Crystal Growth on Starlink, you will partner directly with engineering to rapidly bring online state-of-the-art silicon ingot and wafer fab R&D lines to develop and refine recipes for producing high-quality ingots and wafers. These wafers will feed internal solar cell fabrication for our next generation Starlink satellites and Starship missions to the Moon and Mars. You will be responsible for silicon ingot pulling equipment commissioning, recipe and process development, monitoring and troubleshooting equipment, characterizing ingot and wafer quality, and transferring a stable process to the production teams. RESPONSIBILITIES: - Partner with engineering to rapidly bring online state-of-the art silicon ingot and wafer fab development lines. - Drive equipment setup, calibration, troubleshooting, and maintenance. - Prepare raw materials, seeds, and hot zone components for crystal growth. - Execute DOEs and process trials to inform seeding techniques, recipe optimization, thermal management, impurity control, and defect mitigation. - Perform silicon ingot and wafer characterization; ensure associated lab equipment is maintained and calibrated. - Safely handle chemicals and adhere to all EHS protocols to maintain a safe work environment. - Ensure 5S standards and cleanroom protocols are

Director, Product Management - Access Management Bellevue, Washington; San Francisco, California Secure Every Identity, from AI to Human Identity is the key to unlocking the potential of AI. Okta secures AI by building the trusted, neutral infrastructure that enables organizations to safely embrace this new era. This work requires a relentless drive to solve complex challenges with real-world stakes. We are looking for builders and owners who operate with speed and urgency and execute with excellence. This is an opportunity to do career-defining work. We're all in on this mission. If you are too, let's talk. About the Role Enterprise Access is the authentication and authorization backbone of the Okta Identity Cloud. Every login, every policy evaluation, every federation flow runs through this pillar. The products MFA, SSO, Authentication Policies, Authenticators, Federations (SAML/OIDC/OAuth), XAA Protocol, Customer Identity, Identity Verification, Frontline Worker Authentication, and OIE Upgrade paths, serve billions of monthly authentications across thousands of customers. This PM Director will own the authentication protocols and policies that enable human and non-human identities to authenticate, delegate authority, and interact securely with enterprise resources. You will run Enterprise Access day-to-day: setting roadmap, driving execution, managing a team of 5-7 PMs, and serving as the primary PM voice for this pillar in quarterly planning, cross-pillar coordination, and customer engagements. Success in this role requires a strong ability to understand customer requirements, a deep empathy for user experience, and the ability to strategically prioritize what's most important while managing requests from multiple teams at Okta.

AE - Verification IP, HPC Protocols SAN JOSE posted: Posted 4 Days Ago

Protocol Engineer Vancouver, BC LayerZero The Future is Omnichain. Founded in 2021, LayerZero's vision is to create a community of cross-chain developers, building dApps that are no longer constrained by individual blockchain capabilities. With LayerZero's simple, generic messaging protocol, builders will develop cross-chain dApps designed to unify the power of individual blockchains. We are funded by the best investors in the world including: a16z, Sequoia, PayPal, Binance Ventures, Coinbase Ventures, Uniswap Labs, Circle Ventures, Delphi Digital, and many more. ABOUT THE ROLE As a Protocol Engineer, you'll work on the core infrastructure that underpins decentralized interoperability. You will design and implement core protocol components that operate across heterogeneous chains with rigorous security and performance constraints. You'll be part of a deeply technical team working across LayerZero's protocol and smart contract surface, contributing to novel cross-chain primitives and helping shape the architecture of systems used by some of the most demanding applications in Web3. WHAT YOU'LL DO - Design and implement core protocol contracts and logic on both EVM and non-EVM chains (e.g., message validators, data availability mechanisms, proof verification). - Collaborate with various teams to develop new system primitives, validate security assumptions, and improve protocol robustness. - Own components across their lifecycle: architecture, implementation, testing, deployment, and iteration. - Contribute to high-assurance engineering practices: formal verification, invariant testing, simulation frameworks, fuzzing, and audit readiness. - Investigate emerging cryptographic techniques and novel designs to enhance trust minimization and scalability. - Optimize for correctness and safety in gas-constrained environments, with an emphasis

Lead Product Engineer - MIPI Protocol 2 Locations posted: Posted 30+ Days Ago

Principal Product Engineer - Virtual Protocols SAN JOSE posted: Posted 30+ Days Ago

Principal Protocol Engineer USA - New York City - New York posted: Posted 25 Days Ago

Senior Vulnerability Researcher (5G & Protocol Security) Florham Park, NJ, US posted: Posted 30+ Days Ago

Junior Vulnerability Researcher (5G & Protocol Security) Florham Park, NJ, US posted: Posted 30+ Days Ago

Master Thesis Automated Generative AI Evaluation (f/m/x) Location not specified THE BEST INTERNSHIP IN THEORY - AND IN PRACTICE. SHARE YOUR PASSION. World-leading technologies don't make it into a BMW until they've undergone one of the most challenging journeys imaginable. It takes dynamic teams with outstanding technical skills to take them from the drawing board to the road. That's why our experts will treat you as part of the team from day one, encourage you to bring your own ideas to the table - and give you the opportunity to really show what you can do. We, the BMW Group, focus on benchmarking Generative AI and applying the latest advances in machine learning, computer vision, natural language processing, and human interaction. Our team of experienced AI developers works at the crossroads of AI, specifically Generative AI, machine learning, linguistics, and general computer science to turn science fiction into reality with industrial applications. What awaits you? You will support the development of intelligent and innovative evaluation systems for our in-car LLM and VLM-based systems using generative AI. Furthermore, you help design test scenarios, performance metrics, and validation protocols to assess natural language understanding, multi-agent coordination, Model Context Protocol (MCP) principles, and multimodal context inputs including audio and vision. In addition, your ideas will become an integral part of our product and process portfolios. Moreover, you will contribute to close collaboration with suppliers and internal teams to exchange in

Director, Clinical Science US Remote POSITION SUMMARY: We are seeking a Director, Clinical Science to architect trial strategies and protocol execution for our oncology molecular diagnostics portfolio, with a dedicated focus on signal Studies and pipeline expansion. This clinical leadership role shapes the data validation pipeline for our cell-free DNA (cfDNA) technology, transforming population scale genomic profiles into standard-of-care screening benchmarks. Reporting directly to the Senior Director of Clinical Science, you will lead the strategic alignment and tactical delivery of early and late-stage oncology diagnostics protocols. Operating with an active builder mindset, this position co-develops clinical program strategy and drives collaborative execution across clinical development, clinical operations, biostatistics, and translational data science teams. PRIMARY RESPONSIBILITIES: Trial Strategy and Protocol Architecture - Design robust clinical study concepts, specifying overall design parameters, schedules of assessments, trial objectives, clinical endpoints, and patient eligibility criteria - Lead clinical development activities and protocol design for oncology Signal Studies and portfolio development - Collaborate cross-functionally to author clinical study protocols, informed consent documents, and technical amendments for internal governance review - Deliver technical protocol validation training to internal teams and contract research organizations (CROs), and guide case report form (CRF) layout configurations - Ensure study manuals conform directly to protocol specifications and engage primary clinical investigators during initial trial design phases Data Interrogation and Cross-Functional Alignment - Synthesize protocol requirements from investigators, clinical partners, and regulatory bodies, resolving conflicting operational priorities by anchoring team alignment strictly in data - Partner with cross-functional technical teams to execute

Associate and Experienced Software Engineers - Secure Network & Protocols USA - Oklahoma City, OK posted: Posted 4 Days Ago

Ropes Access Technician (Starship) Starbase, TX SpaceX was founded under the belief that a future where humanity is out exploring the stars is fundamentally more exciting than one where we are not. Today SpaceX is actively developing the technologies to make this possible, with the ultimate goal of enabling human life on Mars. ROPES TECHNICIAN (STARSHIP) The Ropes Access Technician plays a vital role in supporting SpaceX's Starship operations team by executing safe, innovative ropes access solutions in complex, high-stakes environments. This hands-on position involves the precise setup, maintenance, and operation of access systems essential to Starship assembly, testing, and repairs, ensuring the team meets mission-critical objectives with accuracy and safety. By performing technical tasks under supervision, collaborating with engineering and operations teams, participating in qualification training programs, and adhering to stringent safety protocols, the Ropes Access Technician contributes to operational efficiency and the broader success of Starship's mission to advance human space exploration. RESPONSIBILITIES: - Evaluate and develop safe ropes access solutions in new and changing environments - Manage communication, equipment integrity, and process guidelines required for safe ropes access operations - Climb in a variety of environmental conditions to set up ropes access for teammate - Haul team members and equipment using a variety of ropes access configurations - Operate within and enforce SPRAT and IRATA guidelines - Train team members proper use of Ropes Access solutions - Develop rigging for large assemblies - Work at heights on temporary or permanent work access solutions - Operate personnel platforms

Production Operator (Starlink/Akoustis) Canandaigua, NY SpaceX was founded under the belief that a future where humanity is out exploring the stars is fundamentally more exciting than one where we are not. Today SpaceX is actively developing the technologies to make this possible, with the ultimate goal of enabling human life on Mars. PRODUCTION OPERATOR (STARLINK/AKOUSTIS) Akoustis is now operating as a wholly owned subsidiary of SpaceX providing industry leading RF filters using patented XBAW technology to help drive the mission of making human life multi-planetary, while also connecting the world through Starlink. Our work helps further the impact that Starlink is already making on millions of users around the world, while allowing us to broaden that reach dramatically and continue connecting the unconnected here on earth. This production operator position supports RF filter production for SpaceX's Starlink satellite internet constellation and growing defense communications portfolio. An Akoustis Operator operates and monitors complex equipment to fabricate high quality devices in a cleanroom environment. RESPONSIBILITIES: - Operate process equipment to fabricate and characterize devices - Follow work instructions detailed in Manufacturing Execution System (MES) - Document production and statistical process control data - Ensure safety and quality protocols are followed - Communicate issues and suggest improvements to lead or supervisor - Cross train across multiple tool sets - Understand workflow through work center - Understand tool operation and error messages BASIC QUALIFICATIONS: - High school diploma or equivalency certificate PREFERRED SKILLS AND EXPERIENCE: - Associate's degree in technical discipline - Experience working

Process Engineer (Starlink/Akoustis) Canandaigua, NY SpaceX was founded under the belief that a future where humanity is out exploring the stars is fundamentally more exciting than one where we are not. Today SpaceX is actively developing the technologies to make this possible, with the ultimate goal of enabling human life on Mars. PROCESS ENGINEER (STARLINK/AKOUSTIS) Akoustis is now operating as a wholly owned subsidiary of SpaceX providing industry leading RF filters using patented XBAW technology to help drive the mission of making human life multi-planetary, while also connecting the world through Starlink. Our work helps further the impact that Starlink is already making on millions of users around the world, while allowing us to broaden that reach dramatically and continue connecting the unconnected here on earth. This position supports RF filter production for SpaceX's Starlink satellite internet constellation and growing defense communications portfolio. An Akoustis Process Engineer sustains and monitors manufacturing processes to improve yield, quality, and efficiency. RESPONSIBILITIES: - Develop processes to improve efficiency and yield - Analyze data, identify process deviations, and assist in root cause analysis to resolve issues - Perform design of experiments to understand process mapping - Recommend measures to reduce process variation and improve product quality and yield - Assist operations and maintenance teams to maintain, qualify and troubleshoot process and equipment issues - Ensure safety and quality protocols are followed - Review work center SPC charts - Document process specifications and OCAP's - Train operators and technicians BASIC QUALIFICATIONS: - Bachelor's degree in

VP, Clinical Development South San Francisco, CA Company info NewLimit is a biotechnology company working to radically extend human healthspan. We're developing medicines to treat age-related diseases by reprogramming the epigenome, a new therapeutic mechanism to restore regenerative potential in aged and diseased cells. We leverage functional genomics, pooled perturbation screening, and artificial intelligence systems to unravel the biology of aging and disease using experiments of unprecedented scale. Description NewLimit is recruiting a VP of Clinical Development to plan and execute our first clinical trials. Our most advanced assets restore youthful hepatic metabolism and hold the potential to benefit diverse populations with liver disease and metabolic dysfunction. Our early stage programs have similar potential for impact in renal and inflammatory disease indications. In this role, you will design and orchestrate clinical trials for some of the world's first reprogramming medicines. You will serve as the company's senior clinical scientist and as a member of our executive team. As part of your role, you will: - Lead and orchestrate clinical development activities in collaboration with external partners. - Create clinical trial protocols, author and own regulatory submissions, and contribute to regulatory interactions. - Solve the inevitable logistical bottlenecks that block progress of our clinical studies. - Serve as a member of NewLimit's Executive Team and contribute to budgeting, goal setting, and technical review decisions. - Build and run a clinical development team as we approach first-in-human dosing. Requirements - M.D. or equivalent clinical training - Experience planning and orchestrating first-in-human trials

Associate Director, Clinical Science US Remote POSITION SUMMARY: We are seeking an Associate Director, Clinical Science to architect trial strategies and protocol execution for our oncology biobanking studies and specimen repositories. This clinical leadership role shapes the data validation pipeline for our cell-free DNA (cfDNA) technology, transforming population-scale genomic profiles into standard-of-care screening benchmarks. Reporting directly to Neda Huseinovic, Senior Director of Clinical Science, you will lead the strategic alignment and tactical delivery of complex biobanking clinical protocols. Operating with an active builder mindset, this position co-develops clinical program strategy and drives collaborative execution across clinical operations, biostatistics, and translational data science teams, directly managing the clinical scientists embedded within the biobanking workstream. PRIMARY RESPONSIBILITIES: Trial Strategy and Protocol Architecture - Design robust clinical study concepts, specifying overall design parameters, sample-size logic, schedules of assessments, trial objectives, clinical endpoints, and patient eligibility criteria - Lead clinical development activities and protocol design for oncology biobanking studies and biospecimen repository portfolios - Collaborate cross-functionally to author clinical study protocols, informed consent documents (ICFs), and technical amendments for internal governance review - Deliver technical protocol validation training to internal teams and contract research organizations (CROs), and guide case report form (CRF) layout configurations - Ensure study manuals conform directly to protocol specifications and engage primary clinical investigators during initial trial design phases Data Interrogation and Cross-Functional Alignment - Synthesize protocol requirements from investigators, clinical partners, and regulatory bodies, resolving conflicting operational priorities by anchoring team alignment strictly in data - Partner across cross-functional

Lead Product Owner - Sabre Model Context Protocol (MCP) server. Krakow, Małopolskie, Poland posted: Posted 18 Days Ago

Networking Systems Software Engineer (C, C++ - L2/L3 Protocols) Bengaluru, Karnātaka, India Embrace the role of a Networking Systems Software Engineer and help design next-generation network operating systems for high-performance computing. Work with cutting-edge protocols and SDKs, collaborate with top architects, and drive innovation in a hybrid environment. Grow your career with HPE and make an impact in digital transformation.

Software Security Developer (C, C++, Security Protocols) Bengaluru, Karnātaka, India Join our team as a Senior Software Security Developer and lead the design and development of secure, high-performance software systems. Drive innovation in security protocols, cloud architectures, and distributed computing. Collaborate with cross-functional teams to protect critical data and applications in a dynamic, hybrid work environment. Shape the future of secure software with HPE.