iOS Core Product Software Engineer

Speechify seeks an iOS Core Product Software Engineer to join the team in Princeton, NJ. This position centers on building and refining features for Speechify’s iOS applications, with a focus on delivering a smooth and engaging experience for users. Role overview The engineer in this role will design, develop, and maintain essential parts of Speechify’s mobi…

Kardigan is dedicated to improving heart health by pursuing both prevention and cures for cardiovascular disease. The company aims to develop several targeted treatments at once, ensuring people with cardiovascular conditions have more options for care. Founded by Tassos Gianakakos, Jay Edelberg, M.D., Ph.D., and Bob McDowell, Ph.D., Kardigan's leadership previously led MyoKardia to discover and develop mavacamten, the first cardiac myosin inhibitor, which was acquired by Bristol Myers Squibb in 2020. Today, the team continues to advance cardiovascular medicine through a strong research platform and a late-stage pipeline focused on patient outcomes. Our Values Patient-centric: Every decision starts with the needs of patients and their families. Authenticity: Honesty and acceptance shape the work environment. Curiosity: Learning and adapting are part of daily work. Collaborative success: Team members support each other, no matter their role. Unlocking innovation: The team embraces risk to advance care, knowing patients depend on progress. These values guide daily work and reflect the impact the team aims to achieve.

About Us:TransPerfect is dedicated to empowering businesses to thrive in the global marketplace. Recognized as an industry leader, we offer a comprehensive suite of language and business support services tailored to meet the diverse needs of our clients. Our offerings include translation, multicultural marketing, website globalization, legal support, and advanced technology solutions.Your Role:As an Account Manager, you will play a pivotal role in forging new business relationships while providing exceptional support to our existing clients.Key Responsibilities:Conduct thorough research on potential clients utilizing various strategies such as online resources, trade shows, referrals, and professional directories.Compile detailed spreadsheets of prospective client information including names, titles, contact numbers, and addresses.Execute daily outreach to prospective clients using up-to-date data.Engage in cold calling to introduce our services to potential clients.Innovatively enhance our new business development strategies through creative problem-solving.Negotiate project rates and timelines with both prospective and current clients.Inform clients about the translation process, including our pricing, turnaround justifications, and insights on competitors.Collaborate with production teams to ensure that all projects are executed flawlessly and with meticulous attention to detail.Maintain regular follow-ups with clients to guarantee satisfaction with our services.Stay informed about the industries we serve, including key players and relevant market trends.Take on additional special projects or responsibilities as needed.

Join our dynamic team at Fabergent, Inc. as a UI/UX Front-End Architect! We are seeking a passionate and innovative individual with over 14 years of experience in front-end architecture. This full-time position offers the opportunity to work on cutting-edge web applications and create exceptional user experiences.In this role, you will leverage your expertise in AngularJS and JavaScript to design and implement user interfaces that are both functional and visually appealing. Your ability to conceptualize applications as interconnected components, combined with a solid understanding of user behaviors and data interaction, will be crucial to your success.

Join Prosidian Consulting as a Leadership Coach and empower professionals and executives to achieve their full potential. Our coaching services are designed to foster leadership capabilities, enhance decision-making, and drive organizational success. As a Leadership Coach, you will work closely with clients to develop customized coaching plans, facilitate growth-oriented conversations, and provide actionable feedback.

Kyowa Kirin is an innovative global specialty pharmaceutical company, leveraging cutting-edge biotechnologies to discover and deliver groundbreaking therapies across four key disease areas: bone and mineral disorders, intractable hematologic conditions, hematology oncology, and rare diseases. As a company rooted in Japan, our mission is to translate scientific advancements into meaningful patient outcomes by providing effective treatments where options are limited, spanning from drug discovery to product development and market entry. Our North American headquarters is located in Princeton, NJ, with additional offices in California, North Carolina, and Mississauga, Ontario.Position Overview:The Director of Pharmacometrics will spearhead a team of skilled Pharmacometricians within the Global Development Organization (GDO) and the Clinical Pharmacology (CP) function. This role combines direct project involvement with the mentorship of team members in the design and implementation of model-informed drug development (MIDD) strategies. Responsibilities include enhancing workflows and systems for delivering quantitative clinical pharmacology outputs. The Director will play a crucial role in educating project teams and organizational leadership on the significance of MIDD and quantitative clinical pharmacology strategies. Furthermore, the Director will explore collaborative opportunities with various Kyowa Kirin departments, such as Regulatory Affairs and Medical Affairs, to proliferate MIDD strategies throughout the development process and in post-marketing efforts.Key Responsibilities:Oversee pharmacometrics deliverables for project teams, ensuring scientific integrity, timeliness, and substantial impact; identify and capitalize on opportunities to elevate quantitative clinical pharmacology within the organization.Direct pharmacometrics strategy and guarantee high-quality preparation of pharmacometric components for scientific documentation, regulatory submissions, and responses to health authority inquiries.Provide scientific and technical guidance to pharmacometrics staff, ensuring excellence in modeling techniques and effective communication across all organizational tiers.Facilitate clear and impactful communication of pharmacometric and clinical pharmacology findings to diverse internal and external stakeholders.Collaborate with GDO Clinical Pharmacology colleagues and cross-functional partners to enhance efficiency, alignment, and innovation in drug development initiatives.

About Speechify Speechify helps people absorb information in ways that fit their lives. Whether reading articles online, reviewing documents in the cloud, or listening to books on a mobile device, Speechify creates tools that make learning easier. Ranked #1 in our category, we continue to grow quickly as we reshape how audio information is delivered, much like streaming changed audio entertainment. Role Overview: Senior Software Engineer, Core Experiences The Core Experiences Team builds and maintains the core services and SDKs powering Speechify’s products across multiple platforms. This senior engineering role sits at the intersection of product and infrastructure. It suits someone who enjoys shaping both the user experience and the underlying systems, values strategic thinking, and cares about building clear APIs and straightforward, reliable systems. What You Will Do Work closely with Product Teams to define project scopes, improve processes for faster customer feedback, and manage integration and UX trade-offs across teams. Deliver solutions through our cross-platform SDK. Enhance existing features by designing efficient abstractions and refining algorithms to speed up loading times and improve parsing. Build cloud functions, lightweight backend services, and tasks using Kotlin. Who We’re Looking For Systems thinking: Designs with the whole system in mind and values simplicity. Speed: Generates ideas and options quickly, and knows how to prioritize what can be shipped now versus what needs more time. Focus: Can balance engagement with a remote, busy team and deep individual work in a startup setting. Collaboration: Able to inspire, engage, and negotiate with a range of stakeholders, from designers to marketers to product managers. Location Princeton, NJ, USA

About Acadia Pharmaceuticals Acadia Pharmaceuticals focuses on turning scientific discoveries into meaningful treatments for underserved communities affected by neurological and rare diseases. The company’s commercial portfolio includes the first and only FDA-approved therapies for Parkinson’s disease psychosis and Rett syndrome. Acadia continues to advance a diverse pipeline, with mid- and late-stage programs for Alzheimer’s disease psychosis and Lewy body dementia psychosis, as well as early-stage efforts aimed at additional unmet needs. The team is committed to making a real difference in patients’ lives. Location and Work Model This position may be based in San Diego, CA, San Francisco, CA, or Princeton, NJ. Acadia offers a hybrid work model. Role Overview The Executive Director of Translational Sciences leads the design and execution of disease and drug mechanism of action (MoA) studies that advance therapeutics through clinical development. This position requires deep expertise in translational sciences and hands-on experience in rare diseases. Strong leadership and mentoring skills are essential, as well as a thorough understanding of clinical biomarker development and the full drug development process from discovery through late-stage clinical trials. Success in this role depends on the ability to translate complex biological concepts and data into clear, actionable insights. The Executive Director must also demonstrate a record of effective cross-functional collaboration throughout the drug development process.

Join our dynamic team as a Senior Software Engineer in Agentic Engineering at Noom, where we are on a mission to revolutionize the software development lifecycle through innovative autonomous systems.We envision a future where every facet of product development—from brainstorming and prototyping to testing, deployment, and monitoring—is seamlessly powered by intelligent agents. This is not merely a theoretical pursuit; it's a hands-on role where you'll design, develop, and operationalize agent-driven workflows that redefine software creation.As a senior engineer closely integrated within our Engineering team and reporting to the CTO, your work will be pivotal at the crossroads of LLM orchestration, developer tools, and production infrastructure, automating previously manual, human-gated processes into dependable, observable, and autonomous pipelines.

Kyowa Kirin, Inc. is a dynamic and rapidly expanding global specialty pharmaceutical company dedicated to advancing biotechnological innovations to discover and deliver groundbreaking therapies across four critical therapeutic areas: bone and mineral disorders, intractable hematological conditions, hematology oncology, and rare diseases. Headquartered in Princeton, NJ, we aspire to transform scientific breakthroughs into meaningful treatments, ensuring that patients have access to therapies where current options are insufficient. Our North American presence includes additional offices in California, North Carolina, and Mississauga, Ontario. Position Overview: As the Director of Clinical Science (Non-Hemato-Oncology), you will play a pivotal role in our expanding global organization. This leadership position within the Clinical Science group involves collaborating with multi-disciplinary project teams to drive key milestones (such as IND, FIH, POC, EOP2, NDA) for various development programs. You will lead scientific discussions, providing deep insights into the clinical aspects of your assigned programs, and serve as a subject matter expert. In addition, you will actively contribute to the preparation of regulatory documents (e.g., BB, IND), study protocols, and clinical development plans for both new and existing products, while also managing lifecycle strategies. Establishing and nurturing relationships with Key Opinion Leaders (KOLs) will be essential to your success.

Speechify seeks a Senior Software Engineer to focus on Windows and desktop application development. This full-time position is located in Princeton, NJ. Key Responsibilities Design and build desktop applications for Windows platforms Maintain and enhance existing software to ensure reliability and quality Apply software development expertise to deliver robust products Improve user experience through careful engineering and attention to detail Location This role is based in Princeton, New Jersey.

About Acadia Pharmaceuticals Acadia Pharmaceuticals is dedicated to transforming scientific innovations into impactful solutions for underserved neurological and rare disease communities globally. Our commercial portfolio features the first and only FDA-approved therapies for Parkinson’s disease psychosis and Rett syndrome. We are advancing the next wave of therapeutic innovations with a comprehensive and diverse pipeline that includes mid- to late-stage programs in Alzheimer’s disease psychosis and Lewy body dementia psychosis, alongside early-stage initiatives targeting other unmet patient needs. At Acadia, we strive to make a meaningful difference.Opportunities available in: Princeton, NJ and San Diego, CAPosition Overview:The Senior Manager of Clinical Trial Materials is crucial to our clinical development programs, overseeing the planning and execution of Clinical Trial Material (CTM) activities across Phase 1-IV and IIS trials. Responsibilities include demand forecasting, selecting appropriate presentations, establishing production schedules, conducting protocol reviews, ensuring compliance with labeling regulations, developing effective packaging and distribution strategies, monitoring drug supplies, and tracking product retest dates. This role requires collaboration with internal teams and contract research organizations (CROs) to ensure seamless execution of these activities. Additionally, you will implement and uphold group compliance with established procedures for the production and distribution of investigational products while mentoring junior members of the CTM team as necessary.Key Responsibilities:Thoroughly review and interpret clinical protocols or study overviews, providing feedback during protocol development.Calculate total demand and translate that into precise demand forecasts.Collaborate with Project Managers to establish clinical supply timelines, gather study overviews, and define drug requirements to initiate procurement processes.Regularly assess and update inventories, including all supply-related information such as lot numbers, current status, kit genealogy, and expiration dates.