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Senior Level Manager
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Join ACADIA Pharmaceuticals as a Senior Manager of Packaging and Serialization. In this pivotal role, you will lead initiatives to enhance our product packaging and serialization processes, ensuring compliance with industry standards and enhancing operational efficiency. You will collaborate with cross-functional teams to drive innovations in packaging technology and implement best practices across our facilities in Princeton and San Diego.
Full-time|On-site|Princeton, New Jersey, United States; San Diego, California, United States
Join ACADIA Pharmaceuticals as a Senior Manager of Packaging and Serialization. In this pivotal role, you will lead initiatives to enhance our product packaging and serialization processes, ensuring compliance with industry standards and enhancing operational efficiency. You will collaborate with cross-functional teams to drive innovations in packaging techn…
Position Overview:Join our dynamic team as a Senior Validation Project Manager, where you will play a pivotal role as a technical leader. Our ideal candidate possesses a robust background in Commissioning, Qualification, and Validation (CQV) strategy, development, and field execution. At cagents, we prioritize cultural fit, as our people are our greatest asset, and exceptional individuals foster exceptional teams!In this role, you will manage projects exceeding $1 million while leading teams of 6 to 8 engineers and consultants on defined scopes of work. As a successful project manager, you will demonstrate direct accountability for project scope, schedule, and budget. We value experienced generalists, particularly those with expertise in facilities, clean utilities, upstream and downstream biotech equipment, single-use disposables, or aseptic fill-finish manufacturing. While a PMP certification is a plus, your hands-on experience is what will enable you to thrive with our team.Your day-to-day responsibilities may include leading budget review meetings, conducting daily huddles with your team, reviewing summary reports, writing protocols, and providing field support to your team. The role of a CAI PM is multifaceted and requires an active participant—desktop project managers need not apply. Typically, you will report to either a client manager or an area manager.
We are seeking a highly motivated and experienced Senior Product Manager specializing in Information Technology to join our dynamic team. In this role, you will be responsible for leading product strategy, development, and execution in a fast-paced environment. You will work closely with cross-functional teams to deliver innovative solutions that meet customer needs and drive business success.Key responsibilities include defining product vision, prioritizing features, and ensuring alignment with business goals. You will also analyze market trends, gather customer feedback, and collaborate with engineering and design teams to bring products to market effectively.
Full-time|$238K/yr - $297.8K/yr|Hybrid|Princeton, New Jersey, United States; San Diego, California, United States
About Acadia Pharmaceuticals Acadia Pharmaceuticals focuses on turning scientific discoveries into meaningful treatments for people with 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 expand its pipeline, with mid- to late-stage programs in Alzheimer’s disease psychosis and Lewy body dementia psychosis, as well as earlier-stage research targeting additional unmet needs. Location and Hybrid Work Model This Senior Director of Portfolio Management role may be based in Princeton, NJ, San Diego, CA, or South San Francisco, CA. Acadia uses a hybrid work model, with an average of three days per week in the office required for this position. Role Overview The Senior Director of Portfolio Management shapes and executes the strategic direction of Acadia’s development and commercialization portfolio. Working in a matrixed environment, this leader drives portfolio prioritization across the enterprise, builds cross-functional partnerships, and supports effective decision-making to maximize value. The role requires close collaboration with teams in Finance, R&D, and Commercial to ensure portfolio investments align with scientific goals, market needs, and financial discipline. Key Responsibilities Create and apply portfolio prioritization frameworks that balance scientific innovation, commercial opportunity, and financial impact. Partner with Finance to assess investment scenarios, improve resource allocation, and support financially sound portfolio decisions. Work alongside R&D leadership to align pipeline strategy with overall portfolio objectives, focusing on scientific feasibility and milestone-based progress. Collaborate with Commercial teams to incorporate market insights, competitive analysis, and launch planning into product positioning strategies.
Join Ramboll as a Senior Managing Consultant for Air Quality, where you will play a pivotal role in driving sustainable solutions in air quality management. You will collaborate with a diverse team of experts and contribute to innovative projects that address critical environmental challenges. Your expertise will help shape strategies to improve air quality and promote sustainable practices.
Role overview Ensono seeks a Senior Identity and Access Management (IAM) Engineer to join its Princeton, NJ office. This role centers on building, implementing, and supporting IAM solutions that align with business objectives and security needs. What you will do Design and develop IAM systems tailored to organizational requirements and security policies Implement and maintain IAM technologies throughout the company Collaborate with teams across departments to integrate IAM tools and processes Contribute to strengthening security and protecting sensitive data Ensure IAM practices comply with industry standards Enhance user experience while upholding strong access controls Requirements Proven experience in IAM solution design, deployment, and support Ability to work effectively with cross-functional teams Solid understanding of security policies and compliance requirements Dedication to safeguarding sensitive information and refining security processes This position is based in Princeton, NJ.
Full-time|$171K/yr - $223K/yr|On-site|Princeton, New Jersey, United States
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.
Full-time|$150K/yr - $225K/yr|On-site|Princeton, New Jersey, United States
At Withum, we believe that talent flourishes when it is nurtured. Our environment is designed to foster personal and professional growth, where entrepreneurial spirit combined with inclusive teamwork leads to remarkable achievements.Embark on a journey through diverse industries, acquire new skills, and engage with our multifaceted teams to shape your envisioned career path. Your professional journey begins with you!Experience the Transformative Power of Withum Plus You - that’s the Power in the Plus!We are actively looking for an outstanding professional to establish and lead our Tax-focused Food & Beverage Practice in the New York City area, with a primary base in our NYC office. This distinguished leadership position will concentrate on strategic expansion within the Food & Beverage sector, primarily focusing on tax services for multi-unit operators, manufacturers, and distributors.In your role as a Senior Manager, you will act as both a strategic and tactical leader, tasked with developing a high-performing tax team, implementing market strategies, and aligning efforts with our national Industrial & Consumer Products (ICP) team. Collaborating with local office and industry leadership will be essential to ensure market penetration and the visibility of our extensive range of tax services.This is a leadership-first role that demands a dynamic professional with profound tax expertise, exceptional relationship-building capabilities, and a fervor for delivering results in the Food & Beverage industry.Withum’s reputation is a reflection of our people, our culture, and our collective strength. We have become known for our teamwork and excellence in client service. Our success is fundamentally attributed to the dedicated professionals who strive each day to enable our clients to flourish and attain a position of strength. Our commitment extends beyond our clients, as we embody the Withum Way by promoting personal and professional growth for all team members, clients, and the communities we serve.How You’ll Spend Your Time:Driving growth in client base and key industry relationships through proactive market activities.Identifying and pursuing strategic tax planning and compliance opportunities for businesses while ensuring high-quality service delivery aligned with national standards.Providing thought leadership and market insights to both internal and external stakeholders.Maintaining a keen understanding of client tax needs and challenges.
Full-time|$176K/yr - $238K/yr|On-site|New York, New York, United States; Princeton, New Jersey, United States
Noom is dedicated to transforming lives by empowering individuals to achieve healthier lifestyles. As a consumer-driven digital health company, we connect users with tailored content, expert coaching, supportive communities, and access to clinicians to foster sustainable habits that lead to better, longer lives. Our organization is experiencing rapid growth, fueled by scientific insight, cutting-edge technology, and exceptional talent. Joining Noom means making a real impact in the world.Our Product TeamThe Product team at Noom is passionate about creating innovative and engaging user experiences that promote healthier living. By leveraging principles of behavioral psychology, customer feedback, and analytical data, we develop features designed for lasting habit change. In particular, the Engagement Growth Engine team is focused on crafting social experiences, gamification systems, and tools that facilitate daily habit formation, making health engaging and sustainable.About the RoleAs we expand, we are looking for a Senior Product Manager to spearhead the evolution of our social experiences. You will shape the strategic direction and oversee execution for a cross-functional team that drives innovation in social features, gamification, and habit-forming tools. This role demands exceptional product leadership, a comprehensive understanding of user behavior, and the capacity to engage stakeholders across the organization to create high-impact experiences.You WillDefine and advocate for the product vision, strategy, and roadmap for social experiences.Lead comprehensive product execution, balancing immediate delivery with strategic long-term initiatives.Collaborate closely with design, engineering, user research, and analytics teams to launch impactful features that enhance engagement and retention.Analyze user insights, behavioral science, and data to uncover opportunities and influence product strategy.Establish success metrics, assess performance, and iterate based on analytical insights.Guide and align cross-functional stakeholders, prioritizing user needs while meeting business objectives.Mentor and enhance product thinking within the team.About YouIf you are passionate about shaping the future of health through engaging, socially-driven, and habit-forming experiences, and you thrive in a role that merges strategy, execution, and leadership, we encourage you to apply.
Full-time|$139.6K/yr - $174.5K/yr|On-site|Princeton, New Jersey, United States; San Diego, California, United States
About Acadia Pharmaceuticals Acadia Pharmaceuticals is dedicated to transforming scientific potential into innovative solutions that significantly benefit underrepresented communities facing neurological and rare diseases globally. Our commercial offerings include the first and only FDA-approved treatments for Parkinson’s disease psychosis and Rett syndrome. We are at the forefront of developing a new wave of therapeutic innovations with a robust pipeline that encompasses mid- to late-stage programs targeting Alzheimer’s disease psychosis and Lewy body dementia psychosis, as well as earlier-stage programs addressing various unmet patient needs. At Acadia, our mission is to make a tangible difference in patients' lives.We are seeking talent near: Princeton, NJ; San Diego, CAPosition SummaryThe Senior Manager of R&D Learning & Development plays a pivotal role in designing, implementing, and continuously refining onboarding and training strategies, systems training, and learning processes aimed at enhancing scientific, operational, and future-ready capabilities within the Research and Development organization and its pipeline.Primary ResponsibilitiesContribute to the design, implementation, and ongoing enhancement of a comprehensive onboarding and capability-building curriculum that aligns with the dynamic needs of the R&D pipeline, covering discovery, early development, and late-stage programs.Employ experiential learning methodologies to effectively engage adult learners and facilitate successful knowledge transfer.Assist in managing GxP, congress, and data training in collaboration with internal stakeholders.Work collaboratively with R&D subject matter experts to develop focused training on disease areas, modalities, platforms, and pipeline initiatives, including education on investigational assets and emerging scientific advancements.Lead and support training initiatives in partnership with internal stakeholders.Facilitate the management and development of learning modules in collaboration with external vendors.Oversee the creation of advanced, recurrent, and future-focused training materials.
Full-time|$124.2K/yr - $155.2K/yr|On-site|Princeton, New Jersey, United States; San Diego, California, United States
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.
Full-time|$225K/yr - $265K/yr|On-site|New York, New York, United States; Princeton, New Jersey, United States
Noom is dedicated to empowering individuals to lead healthier, longer lives. As an innovative digital health company, we connect our users with valuable content, personalized coaching, community support, and medical professionals to foster sustainable health habits. Our organization thrives on a foundation of scientific research, cutting-edge technology, and exceptional talent, ensuring that every team member can witness the meaningful impact of their contributions.About the RoleAs part of our expansion, we are looking for a Senior Director of Clinical Operations to spearhead and enhance our clinical operations division. Reporting directly to the SVP of Health Operations and Customer Experience, you will inherit a dedicated team and an active portfolio of initiatives, while also creating new strategies. You will be responsible for overseeing clinical protocols, managing vendor relationships, and developing operational frameworks that bring Noom’s clinical programs to fruition for both B2B and direct-to-consumer markets.Your ResponsibilitiesOversee the comprehensive clinical operations organization for Noom Med, facilitating strategic growth in clinical programs, protocol development, and the execution of new initiatives alongside Product and Engineering teams.Act as the operational liaison between clinical strategy and implementation, ensuring that commitments to members and enterprise partners are met with excellence, accuracy, and quantifiable results.Build and lead a high-performing clinical operations team, managing recruitment strategies and headcount as the company scales.Drive the execution of clinical programs across D2C and B2B initiatives, fostering collaboration among internal clinical teams, external provider networks, and vendor partners.Ensure a positive provider and member experience, prioritizing provider satisfaction, clinical quality, and member health outcomes as key performance indicators.Establish and maintain the operational infrastructure that supports the clinical organization, including capacity models, utilization targets, reporting systems, and workflow processes that adapt to growth.Continuously evolve your role and responsibilities to meet the demands of Noom Med's expansion.
As a Senior IT Auditor, you will provide independent and objective evaluations of the effectiveness and efficiency of our internal controls, designed to mitigate business risks and enhance performance objectives and strategy. Additionally, you will offer assurance services as requested by Senior Management or the Audit Committee.Key Responsibilities:Conduct IT and integrated audits by defining audit objectives, creating timelines, and customizing audit programs.Prepare comprehensive audit work papers and reports by documenting tests and findings.Facilitate the external audit process by coordinating information requests and participating in audits led by external auditors.Assist with compliance areas such as Sarbanes-Oxley, internal controls, and remediation efforts as needed.Help develop and implement training programs focusing on risk management, ethical practices, and anti-fraud measures.Perform audit walkthroughs and detailed control evaluations; summarize audit results and complete documentation. Communicate audit observations and recommendations to diverse audiences.Support the department with data analytics and system access.
We are on the lookout for a highly skilled Senior Tax Accountant with exceptional professional capabilities and potential for partnership. This role involves substantial interaction with clients and engagement partners, providing strategic advice and becoming a trusted business advisor. The ideal candidate will excel in managing engagements and fostering strong client relationships. Experience with compilation and review engagements is preferred, though not mandatory.
Join Ramboll as a Senior Consultant specializing in Air Quality, where your expertise will directly contribute to environmental sustainability. In this pivotal role, you will leverage your analytical skills to assess air quality data and formulate strategies aimed at improving air quality standards. Collaborate with a dynamic team of professionals dedicated to advancing environmental solutions.
Full-time|$99K/yr - $116.5K/yr|Hybrid|Princeton, New Jersey, United States
Position OverviewThe Senior Tax Planning Analyst will report directly to the Senior Manager of Tax Planning. This role involves providing crucial support in various tax planning initiatives, particularly focusing on US federal and state income tax, transaction tax return assistance, cash tax optimization, and evaluating credits and incentives.This is a hybrid position with a preferred base location in our Scottsdale office. If you believe you can contribute to this role even if you don't meet all the qualifications, we encourage you to apply.Key ResponsibilitiesCalculate tax basis, 704(b) capital accounts, and transaction-related impacts, providing comprehensive explanations for tax compliance.Prepare detailed memos and presentations to document transaction diligence.Review financial models encompassing cash taxes, partnership capital accounts, and related credits and incentives.Conduct tax research on unique tax fact patterns.Work closely with Accounting, Business Development, and Portfolio Finance teams to support transactions and ensure accurate tax modeling.Proactively drive process improvements to enhance tax planning efficiency.QualificationsBachelor’s Degree in Accounting, Finance, Business, Taxation, or related fields.At least 4 years of relevant professional experience.2-3 years of experience in federal and state tax compliance or tax planning within a public accounting firm or large corporate tax department.Experience with partnership (Sub K) tax.A strong desire to learn data analytics tools such as Power BI, Alteryx, and Excel.Ability to collaborate cross-functionally and communicate tax concepts to non-tax stakeholders effectively.Strong organizational skills to manage multiple tasks while delivering high-quality results on time.Excellent analytical and Excel modeling skills, with proficiency in PowerPoint.Preferred SkillsFamiliarity with advanced tax software and tools.
Full-time|$235.6K/yr - $294.5K/yr|Hybrid|Princeton, New Jersey, United States; San Diego, California, United States
About Acadia Pharmaceuticals Acadia Pharmaceuticals is dedicated to transforming scientific innovation into impactful solutions for underserved communities affected by neurological and rare diseases across the globe. Our commercial portfolio features the pioneering and sole FDA-approved treatments for Parkinson's disease psychosis and Rett syndrome. We are advancing the next generation of therapeutic breakthroughs with a robust pipeline that spans mid- to late-stage programs in Alzheimer’s disease psychosis and Lewy body dementia psychosis, alongside early-stage initiatives targeting other critical patient needs. At Acadia, we are committed to making a difference.This position is available in either San Diego, CA, or Princeton, NJ. Acadia operates on a hybrid model, requiring this role to be in the office an average of three days per week.
Full-time|$85K/yr - $110K/yr|On-site|East Brunswick, New Jersey, United States; New York, New York, United States; Philadelphia, Pennsylvania, United States; Princeton, New Jersey, United States; Whippany, New Jersey, United States
WithumSmithBrown values individuality and talent. The firm supports growth and encourages team members to bring their full selves to work. Collaboration and an entrepreneurial mindset shape the way teams approach client service and professional development. The System and Process Assurance team is growing to meet increased demand for assurance services. Withum is hiring a Senior Consultant for Contract Compliance. This position focuses on contract compliance audits, including royalty, franchise, revenue participation, lease agreement, and vendor audits, as well as other contractual projects. The role can be based in New York, NY; Whippany, NJ; East Brunswick, NJ; Red Bank, NJ; Princeton, NJ; or Philadelphia, PA. Withum’s culture centers on teamwork, resilience, and a commitment to helping clients and communities thrive. The firm invests in both personal and professional growth for all team members. Learn more about the Withum Way. What You Will Do Assist audit teams with planning and evaluating franchisees’ and licensees’ compliance with financial and brand management requirements during contract compliance audits. Review financial records of franchisees and licensees to determine reportable income and fulfillment of other contractual obligations. Conduct independent research on franchisees, owners, and related parties to understand contractual relationships. Manage project workflow to meet deadlines and maintain effective communication with clients for cooperation throughout the process. Prepare work papers that summarize findings, conclusions, and outcomes for clients. Document franchisees’ and licensees’ responses to evaluations and verify compliance with contract terms.
Full-time|On-site|Princeton, New Jersey, United States
We are seeking a highly experienced and strategic Senior Director of Drug Substance Development to lead our innovative team at Kardigan in Princeton, New Jersey. In this pivotal role, you will spearhead the development of drug substances from early-stage formulation through to commercialization, ensuring that our products meet the highest standards of quality and efficacy. The ideal candidate will possess a deep understanding of drug development processes, project management, regulatory requirements, and cross-functional collaboration. You will drive initiatives that enhance productivity and foster a culture of scientific excellence, providing mentorship and guidance to team members.
Full-time|$263K/yr - $357K/yr|On-site|South San Francisco, California, United States, Princeton, New Jersey, United States
About Kardigan Kardigan focuses on heart health, working to shift cardiovascular disease from a global threat to a manageable condition. The company develops multiple targeted therapies at once, aiming to provide effective treatments for people living with cardiovascular diseases. Kardigan was founded by Tassos Gianakakos, Jay Edelberg, M.D., Ph.D., and Bob McDowell, Ph.D. The team previously led MyoKardia, where they developed mavacamten, the first cardiac myosin inhibitor. Their work led to MyoKardia's acquisition by Bristol Myers Squibb in 2020. The company uses advanced discovery and translational research platforms and has a pipeline of late-stage candidates. The team is committed to improving patient outcomes. Our Values Prioritize the well-being of patients and their families Embrace authenticity and foster inclusion Encourage learning, curiosity, and adaptability Support each other in striving for excellence Work together to achieve ambitious goals for patients These values shape daily work at Kardigan and support a lasting impact in the field of cardiovascular health.
Full-time|On-site|Princeton, New Jersey, United States; San Diego, California, United States
Join ACADIA Pharmaceuticals as a Senior Manager of Packaging and Serialization. In this pivotal role, you will lead initiatives to enhance our product packaging and serialization processes, ensuring compliance with industry standards and enhancing operational efficiency. You will collaborate with cross-functional teams to drive innovations in packaging techn…
Position Overview:Join our dynamic team as a Senior Validation Project Manager, where you will play a pivotal role as a technical leader. Our ideal candidate possesses a robust background in Commissioning, Qualification, and Validation (CQV) strategy, development, and field execution. At cagents, we prioritize cultural fit, as our people are our greatest asset, and exceptional individuals foster exceptional teams!In this role, you will manage projects exceeding $1 million while leading teams of 6 to 8 engineers and consultants on defined scopes of work. As a successful project manager, you will demonstrate direct accountability for project scope, schedule, and budget. We value experienced generalists, particularly those with expertise in facilities, clean utilities, upstream and downstream biotech equipment, single-use disposables, or aseptic fill-finish manufacturing. While a PMP certification is a plus, your hands-on experience is what will enable you to thrive with our team.Your day-to-day responsibilities may include leading budget review meetings, conducting daily huddles with your team, reviewing summary reports, writing protocols, and providing field support to your team. The role of a CAI PM is multifaceted and requires an active participant—desktop project managers need not apply. Typically, you will report to either a client manager or an area manager.
We are seeking a highly motivated and experienced Senior Product Manager specializing in Information Technology to join our dynamic team. In this role, you will be responsible for leading product strategy, development, and execution in a fast-paced environment. You will work closely with cross-functional teams to deliver innovative solutions that meet customer needs and drive business success.Key responsibilities include defining product vision, prioritizing features, and ensuring alignment with business goals. You will also analyze market trends, gather customer feedback, and collaborate with engineering and design teams to bring products to market effectively.
Full-time|$238K/yr - $297.8K/yr|Hybrid|Princeton, New Jersey, United States; San Diego, California, United States
About Acadia Pharmaceuticals Acadia Pharmaceuticals focuses on turning scientific discoveries into meaningful treatments for people with 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 expand its pipeline, with mid- to late-stage programs in Alzheimer’s disease psychosis and Lewy body dementia psychosis, as well as earlier-stage research targeting additional unmet needs. Location and Hybrid Work Model This Senior Director of Portfolio Management role may be based in Princeton, NJ, San Diego, CA, or South San Francisco, CA. Acadia uses a hybrid work model, with an average of three days per week in the office required for this position. Role Overview The Senior Director of Portfolio Management shapes and executes the strategic direction of Acadia’s development and commercialization portfolio. Working in a matrixed environment, this leader drives portfolio prioritization across the enterprise, builds cross-functional partnerships, and supports effective decision-making to maximize value. The role requires close collaboration with teams in Finance, R&D, and Commercial to ensure portfolio investments align with scientific goals, market needs, and financial discipline. Key Responsibilities Create and apply portfolio prioritization frameworks that balance scientific innovation, commercial opportunity, and financial impact. Partner with Finance to assess investment scenarios, improve resource allocation, and support financially sound portfolio decisions. Work alongside R&D leadership to align pipeline strategy with overall portfolio objectives, focusing on scientific feasibility and milestone-based progress. Collaborate with Commercial teams to incorporate market insights, competitive analysis, and launch planning into product positioning strategies.
Join Ramboll as a Senior Managing Consultant for Air Quality, where you will play a pivotal role in driving sustainable solutions in air quality management. You will collaborate with a diverse team of experts and contribute to innovative projects that address critical environmental challenges. Your expertise will help shape strategies to improve air quality and promote sustainable practices.
Role overview Ensono seeks a Senior Identity and Access Management (IAM) Engineer to join its Princeton, NJ office. This role centers on building, implementing, and supporting IAM solutions that align with business objectives and security needs. What you will do Design and develop IAM systems tailored to organizational requirements and security policies Implement and maintain IAM technologies throughout the company Collaborate with teams across departments to integrate IAM tools and processes Contribute to strengthening security and protecting sensitive data Ensure IAM practices comply with industry standards Enhance user experience while upholding strong access controls Requirements Proven experience in IAM solution design, deployment, and support Ability to work effectively with cross-functional teams Solid understanding of security policies and compliance requirements Dedication to safeguarding sensitive information and refining security processes This position is based in Princeton, NJ.
Full-time|$171K/yr - $223K/yr|On-site|Princeton, New Jersey, United States
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.
Full-time|$150K/yr - $225K/yr|On-site|Princeton, New Jersey, United States
At Withum, we believe that talent flourishes when it is nurtured. Our environment is designed to foster personal and professional growth, where entrepreneurial spirit combined with inclusive teamwork leads to remarkable achievements.Embark on a journey through diverse industries, acquire new skills, and engage with our multifaceted teams to shape your envisioned career path. Your professional journey begins with you!Experience the Transformative Power of Withum Plus You - that’s the Power in the Plus!We are actively looking for an outstanding professional to establish and lead our Tax-focused Food & Beverage Practice in the New York City area, with a primary base in our NYC office. This distinguished leadership position will concentrate on strategic expansion within the Food & Beverage sector, primarily focusing on tax services for multi-unit operators, manufacturers, and distributors.In your role as a Senior Manager, you will act as both a strategic and tactical leader, tasked with developing a high-performing tax team, implementing market strategies, and aligning efforts with our national Industrial & Consumer Products (ICP) team. Collaborating with local office and industry leadership will be essential to ensure market penetration and the visibility of our extensive range of tax services.This is a leadership-first role that demands a dynamic professional with profound tax expertise, exceptional relationship-building capabilities, and a fervor for delivering results in the Food & Beverage industry.Withum’s reputation is a reflection of our people, our culture, and our collective strength. We have become known for our teamwork and excellence in client service. Our success is fundamentally attributed to the dedicated professionals who strive each day to enable our clients to flourish and attain a position of strength. Our commitment extends beyond our clients, as we embody the Withum Way by promoting personal and professional growth for all team members, clients, and the communities we serve.How You’ll Spend Your Time:Driving growth in client base and key industry relationships through proactive market activities.Identifying and pursuing strategic tax planning and compliance opportunities for businesses while ensuring high-quality service delivery aligned with national standards.Providing thought leadership and market insights to both internal and external stakeholders.Maintaining a keen understanding of client tax needs and challenges.
Full-time|$176K/yr - $238K/yr|On-site|New York, New York, United States; Princeton, New Jersey, United States
Noom is dedicated to transforming lives by empowering individuals to achieve healthier lifestyles. As a consumer-driven digital health company, we connect users with tailored content, expert coaching, supportive communities, and access to clinicians to foster sustainable habits that lead to better, longer lives. Our organization is experiencing rapid growth, fueled by scientific insight, cutting-edge technology, and exceptional talent. Joining Noom means making a real impact in the world.Our Product TeamThe Product team at Noom is passionate about creating innovative and engaging user experiences that promote healthier living. By leveraging principles of behavioral psychology, customer feedback, and analytical data, we develop features designed for lasting habit change. In particular, the Engagement Growth Engine team is focused on crafting social experiences, gamification systems, and tools that facilitate daily habit formation, making health engaging and sustainable.About the RoleAs we expand, we are looking for a Senior Product Manager to spearhead the evolution of our social experiences. You will shape the strategic direction and oversee execution for a cross-functional team that drives innovation in social features, gamification, and habit-forming tools. This role demands exceptional product leadership, a comprehensive understanding of user behavior, and the capacity to engage stakeholders across the organization to create high-impact experiences.You WillDefine and advocate for the product vision, strategy, and roadmap for social experiences.Lead comprehensive product execution, balancing immediate delivery with strategic long-term initiatives.Collaborate closely with design, engineering, user research, and analytics teams to launch impactful features that enhance engagement and retention.Analyze user insights, behavioral science, and data to uncover opportunities and influence product strategy.Establish success metrics, assess performance, and iterate based on analytical insights.Guide and align cross-functional stakeholders, prioritizing user needs while meeting business objectives.Mentor and enhance product thinking within the team.About YouIf you are passionate about shaping the future of health through engaging, socially-driven, and habit-forming experiences, and you thrive in a role that merges strategy, execution, and leadership, we encourage you to apply.
Full-time|$139.6K/yr - $174.5K/yr|On-site|Princeton, New Jersey, United States; San Diego, California, United States
About Acadia Pharmaceuticals Acadia Pharmaceuticals is dedicated to transforming scientific potential into innovative solutions that significantly benefit underrepresented communities facing neurological and rare diseases globally. Our commercial offerings include the first and only FDA-approved treatments for Parkinson’s disease psychosis and Rett syndrome. We are at the forefront of developing a new wave of therapeutic innovations with a robust pipeline that encompasses mid- to late-stage programs targeting Alzheimer’s disease psychosis and Lewy body dementia psychosis, as well as earlier-stage programs addressing various unmet patient needs. At Acadia, our mission is to make a tangible difference in patients' lives.We are seeking talent near: Princeton, NJ; San Diego, CAPosition SummaryThe Senior Manager of R&D Learning & Development plays a pivotal role in designing, implementing, and continuously refining onboarding and training strategies, systems training, and learning processes aimed at enhancing scientific, operational, and future-ready capabilities within the Research and Development organization and its pipeline.Primary ResponsibilitiesContribute to the design, implementation, and ongoing enhancement of a comprehensive onboarding and capability-building curriculum that aligns with the dynamic needs of the R&D pipeline, covering discovery, early development, and late-stage programs.Employ experiential learning methodologies to effectively engage adult learners and facilitate successful knowledge transfer.Assist in managing GxP, congress, and data training in collaboration with internal stakeholders.Work collaboratively with R&D subject matter experts to develop focused training on disease areas, modalities, platforms, and pipeline initiatives, including education on investigational assets and emerging scientific advancements.Lead and support training initiatives in partnership with internal stakeholders.Facilitate the management and development of learning modules in collaboration with external vendors.Oversee the creation of advanced, recurrent, and future-focused training materials.
Full-time|$124.2K/yr - $155.2K/yr|On-site|Princeton, New Jersey, United States; San Diego, California, United States
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.
Full-time|$225K/yr - $265K/yr|On-site|New York, New York, United States; Princeton, New Jersey, United States
Noom is dedicated to empowering individuals to lead healthier, longer lives. As an innovative digital health company, we connect our users with valuable content, personalized coaching, community support, and medical professionals to foster sustainable health habits. Our organization thrives on a foundation of scientific research, cutting-edge technology, and exceptional talent, ensuring that every team member can witness the meaningful impact of their contributions.About the RoleAs part of our expansion, we are looking for a Senior Director of Clinical Operations to spearhead and enhance our clinical operations division. Reporting directly to the SVP of Health Operations and Customer Experience, you will inherit a dedicated team and an active portfolio of initiatives, while also creating new strategies. You will be responsible for overseeing clinical protocols, managing vendor relationships, and developing operational frameworks that bring Noom’s clinical programs to fruition for both B2B and direct-to-consumer markets.Your ResponsibilitiesOversee the comprehensive clinical operations organization for Noom Med, facilitating strategic growth in clinical programs, protocol development, and the execution of new initiatives alongside Product and Engineering teams.Act as the operational liaison between clinical strategy and implementation, ensuring that commitments to members and enterprise partners are met with excellence, accuracy, and quantifiable results.Build and lead a high-performing clinical operations team, managing recruitment strategies and headcount as the company scales.Drive the execution of clinical programs across D2C and B2B initiatives, fostering collaboration among internal clinical teams, external provider networks, and vendor partners.Ensure a positive provider and member experience, prioritizing provider satisfaction, clinical quality, and member health outcomes as key performance indicators.Establish and maintain the operational infrastructure that supports the clinical organization, including capacity models, utilization targets, reporting systems, and workflow processes that adapt to growth.Continuously evolve your role and responsibilities to meet the demands of Noom Med's expansion.
As a Senior IT Auditor, you will provide independent and objective evaluations of the effectiveness and efficiency of our internal controls, designed to mitigate business risks and enhance performance objectives and strategy. Additionally, you will offer assurance services as requested by Senior Management or the Audit Committee.Key Responsibilities:Conduct IT and integrated audits by defining audit objectives, creating timelines, and customizing audit programs.Prepare comprehensive audit work papers and reports by documenting tests and findings.Facilitate the external audit process by coordinating information requests and participating in audits led by external auditors.Assist with compliance areas such as Sarbanes-Oxley, internal controls, and remediation efforts as needed.Help develop and implement training programs focusing on risk management, ethical practices, and anti-fraud measures.Perform audit walkthroughs and detailed control evaluations; summarize audit results and complete documentation. Communicate audit observations and recommendations to diverse audiences.Support the department with data analytics and system access.
We are on the lookout for a highly skilled Senior Tax Accountant with exceptional professional capabilities and potential for partnership. This role involves substantial interaction with clients and engagement partners, providing strategic advice and becoming a trusted business advisor. The ideal candidate will excel in managing engagements and fostering strong client relationships. Experience with compilation and review engagements is preferred, though not mandatory.
Join Ramboll as a Senior Consultant specializing in Air Quality, where your expertise will directly contribute to environmental sustainability. In this pivotal role, you will leverage your analytical skills to assess air quality data and formulate strategies aimed at improving air quality standards. Collaborate with a dynamic team of professionals dedicated to advancing environmental solutions.
Full-time|$99K/yr - $116.5K/yr|Hybrid|Princeton, New Jersey, United States
Position OverviewThe Senior Tax Planning Analyst will report directly to the Senior Manager of Tax Planning. This role involves providing crucial support in various tax planning initiatives, particularly focusing on US federal and state income tax, transaction tax return assistance, cash tax optimization, and evaluating credits and incentives.This is a hybrid position with a preferred base location in our Scottsdale office. If you believe you can contribute to this role even if you don't meet all the qualifications, we encourage you to apply.Key ResponsibilitiesCalculate tax basis, 704(b) capital accounts, and transaction-related impacts, providing comprehensive explanations for tax compliance.Prepare detailed memos and presentations to document transaction diligence.Review financial models encompassing cash taxes, partnership capital accounts, and related credits and incentives.Conduct tax research on unique tax fact patterns.Work closely with Accounting, Business Development, and Portfolio Finance teams to support transactions and ensure accurate tax modeling.Proactively drive process improvements to enhance tax planning efficiency.QualificationsBachelor’s Degree in Accounting, Finance, Business, Taxation, or related fields.At least 4 years of relevant professional experience.2-3 years of experience in federal and state tax compliance or tax planning within a public accounting firm or large corporate tax department.Experience with partnership (Sub K) tax.A strong desire to learn data analytics tools such as Power BI, Alteryx, and Excel.Ability to collaborate cross-functionally and communicate tax concepts to non-tax stakeholders effectively.Strong organizational skills to manage multiple tasks while delivering high-quality results on time.Excellent analytical and Excel modeling skills, with proficiency in PowerPoint.Preferred SkillsFamiliarity with advanced tax software and tools.
Full-time|$235.6K/yr - $294.5K/yr|Hybrid|Princeton, New Jersey, United States; San Diego, California, United States
About Acadia Pharmaceuticals Acadia Pharmaceuticals is dedicated to transforming scientific innovation into impactful solutions for underserved communities affected by neurological and rare diseases across the globe. Our commercial portfolio features the pioneering and sole FDA-approved treatments for Parkinson's disease psychosis and Rett syndrome. We are advancing the next generation of therapeutic breakthroughs with a robust pipeline that spans mid- to late-stage programs in Alzheimer’s disease psychosis and Lewy body dementia psychosis, alongside early-stage initiatives targeting other critical patient needs. At Acadia, we are committed to making a difference.This position is available in either San Diego, CA, or Princeton, NJ. Acadia operates on a hybrid model, requiring this role to be in the office an average of three days per week.
Full-time|$85K/yr - $110K/yr|On-site|East Brunswick, New Jersey, United States; New York, New York, United States; Philadelphia, Pennsylvania, United States; Princeton, New Jersey, United States; Whippany, New Jersey, United States
WithumSmithBrown values individuality and talent. The firm supports growth and encourages team members to bring their full selves to work. Collaboration and an entrepreneurial mindset shape the way teams approach client service and professional development. The System and Process Assurance team is growing to meet increased demand for assurance services. Withum is hiring a Senior Consultant for Contract Compliance. This position focuses on contract compliance audits, including royalty, franchise, revenue participation, lease agreement, and vendor audits, as well as other contractual projects. The role can be based in New York, NY; Whippany, NJ; East Brunswick, NJ; Red Bank, NJ; Princeton, NJ; or Philadelphia, PA. Withum’s culture centers on teamwork, resilience, and a commitment to helping clients and communities thrive. The firm invests in both personal and professional growth for all team members. Learn more about the Withum Way. What You Will Do Assist audit teams with planning and evaluating franchisees’ and licensees’ compliance with financial and brand management requirements during contract compliance audits. Review financial records of franchisees and licensees to determine reportable income and fulfillment of other contractual obligations. Conduct independent research on franchisees, owners, and related parties to understand contractual relationships. Manage project workflow to meet deadlines and maintain effective communication with clients for cooperation throughout the process. Prepare work papers that summarize findings, conclusions, and outcomes for clients. Document franchisees’ and licensees’ responses to evaluations and verify compliance with contract terms.
Full-time|On-site|Princeton, New Jersey, United States
We are seeking a highly experienced and strategic Senior Director of Drug Substance Development to lead our innovative team at Kardigan in Princeton, New Jersey. In this pivotal role, you will spearhead the development of drug substances from early-stage formulation through to commercialization, ensuring that our products meet the highest standards of quality and efficacy. The ideal candidate will possess a deep understanding of drug development processes, project management, regulatory requirements, and cross-functional collaboration. You will drive initiatives that enhance productivity and foster a culture of scientific excellence, providing mentorship and guidance to team members.
Full-time|$263K/yr - $357K/yr|On-site|South San Francisco, California, United States, Princeton, New Jersey, United States
About Kardigan Kardigan focuses on heart health, working to shift cardiovascular disease from a global threat to a manageable condition. The company develops multiple targeted therapies at once, aiming to provide effective treatments for people living with cardiovascular diseases. Kardigan was founded by Tassos Gianakakos, Jay Edelberg, M.D., Ph.D., and Bob McDowell, Ph.D. The team previously led MyoKardia, where they developed mavacamten, the first cardiac myosin inhibitor. Their work led to MyoKardia's acquisition by Bristol Myers Squibb in 2020. The company uses advanced discovery and translational research platforms and has a pipeline of late-stage candidates. The team is committed to improving patient outcomes. Our Values Prioritize the well-being of patients and their families Embrace authenticity and foster inclusion Encourage learning, curiosity, and adaptability Support each other in striving for excellence Work together to achieve ambitious goals for patients These values shape daily work at Kardigan and support a lasting impact in the field of cardiovascular health.