Dynamic Account Manager

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 adv…

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.

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.

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.

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.

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’s mission is simple: make sure reading never stands in the way of learning. Over 50 million people use Speechify to turn text from PDFs, books, Google Docs, news articles, and websites into audio. This helps users read faster, understand more, and remember what matters. Our products span iOS, Android, Mac, Chrome, and the web. Recent honors include Google’s Chrome Extension of the Year and Apple’s 2025 Design Award for Inclusivity. The company operates fully remotely, with nearly 200 team members worldwide. Our engineers, AI researchers, and specialists come from places like Amazon, Microsoft, Google, Stanford, Stripe, Vercel, and Bolt. Role Overview Speechify’s Android app leads the Play Store in text-to-speech. As our user base grows, we’re looking for a Tech Lead for the Android Core Product to help shape the future of the app and support our ongoing expansion. This senior role suits someone who thinks strategically, enjoys building products, and values outstanding user experiences. The team values technical leadership shown through results, not hierarchy. Strong communication, reliability, and a drive to deliver are key. What You Will Do Own major Android app features and work closely with designers to ship high-quality updates. Help set the strategic direction for the Android team. Monitor and improve reliability metrics for core features. Collaborate across Product, Design, and Engineering teams. Review pull requests and mentor team members. Troubleshoot critical issues and adapt to new challenges as they arise. Interview Process The interview process includes several technical interviews, typically completed within one week. Location This role is based in Princeton, NJ, USA.

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.

Join our dynamic team at Ramboll as a Principal Air Quality Specialist. In this pivotal role, you will leverage your extensive expertise in air quality management to lead innovative projects that enhance environmental performance and compliance. Collaborate with a diverse team of professionals to develop sustainable solutions that address complex air quality challenges.Your contributions will be vital in shaping our approach to air quality assessments, regulatory compliance, and stakeholder engagement. As a leader in the field, you will have the opportunity to mentor junior staff and contribute to the development of best practices within the industry.