Associate Consultant

We are seeking a dynamic and motivated Associate Consultant to join our team at Ramboll Group. In this role, you will engage in various projects that drive impactful change across multiple sectors. You will collaborate with experienced consultants, gaining valuable insights and developing your professional skills. This is an excellent opportunity for individ…

Join our dynamic team at Sonsoft Inc. as a QUMAS Consultant, where you will play a crucial role in enhancing our clients' regulatory compliance and quality management systems. As an integral part of our consulting team, you will leverage your expertise to implement effective QUMAS solutions, ensuring that our clients meet industry standards and regulations. This position offers an exciting opportunity to work with cutting-edge technology and contribute to the success of various projects.

About Beghou Consulting Beghou Consulting partners with life sciences companies to strengthen commercialization strategies. Drawing on more than thirty years of experience, the team delivers strategic insights, advanced analytics, and technology solutions. Services include go-to-market planning, building data analytics frameworks, and applying artificial intelligence to deepen customer understanding and engagement. Clients benefit from both proprietary and third-party technology that supports accurate forecasting, territory design, and careful management and reporting of medical and commercial data. Beghou Consulting’s mission: combine analytical expertise with technology to help life sciences companies navigate healthcare’s complexities and improve patient outcomes. Role Overview: Consultant – Data Management Based in Princeton, New Jersey, the Consultant will shape and deliver data-driven projects supporting commercial initiatives in the pharmaceutical and life sciences space. This role involves leading innovation, developing creative solutions, and providing thought leadership across multiple workstreams. The Consultant will guide project teams and help internal stakeholders meet project goals.

Join our dynamic team at Ramboll as a Managing Consultant in Air Quality, where you will leverage your expertise to drive impactful environmental solutions. In this pivotal role, you will lead projects that enhance air quality standards, working closely with a diverse range of clients including governmental agencies and private sector organizations.Your responsibilities will include developing innovative strategies, collaborating with multidisciplinary teams, and ensuring compliance with regulatory frameworks. This position offers a unique opportunity to make a significant difference in environmental management and public health.

Join Ramboll as a Managing Consultant or Senior Managing Consultant specializing in M&A Environmental Due Diligence. In this pivotal role, you will leverage your expertise to guide clients through complex environmental assessments related to mergers and acquisitions. Your strategic insights will be essential in ensuring compliance and mitigating risks while promoting sustainable business practices.

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.

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.

We are seeking a skilled Regulatory Publishing Consultant to join our team. In this role, you will leverage your expertise in regulatory publishing to ensure compliance and enhance the quality of our publications. Your insights will be crucial in navigating regulatory frameworks and contributing to successful project outcomes.

Join our dynamic team at Sonsoft Inc. as an Informatica MDM Consultant. In this role, you will leverage your expertise in Master Data Management (MDM) using Informatica solutions to help our clients optimize their data management processes. You will work closely with stakeholders to gather requirements, design data models, and implement data governance strategies.

Join Coface as a Business Information Solutions Consultant, where you will leverage your analytical skills and industry knowledge to provide innovative solutions that empower our clients. You will work closely with cross-functional teams to deliver exceptional service and insights, ensuring our clients achieve their business objectives efficiently.

Join Ramboll as a Managing Consultant in Acoustics, where you will leverage your expertise to provide innovative acoustic solutions. In this role, you will lead projects, engage with clients, and contribute to our mission of creating sustainable environments through advanced acoustic engineering.

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.

About Us Kardigan is at the forefront of heart health innovation, aiming to transform cardiovascular disease into a preventable and curable condition, ultimately striving to eliminate it as a leading cause of death worldwide.Our mission is to develop a range of targeted treatments simultaneously, ensuring individuals with cardiovascular diseases can access the cures they rightfully deserve. Founded by industry leaders Tassos Giannakakos, Jay Edelberg, M.D., Ph.D., and Bob McDowell, Ph.D., Kardigan has reunited after their successful journey at MyoKardia, where they pioneered mavacamten, the first cardiac myosin inhibitor, culminating in its acquisition by Bristol Myers Squibb in 2020. With a state-of-the-art discovery and translational research platform and a pipeline of late-stage candidates, our exceptional team is dedicated to enhancing patient lives. At Kardigan, our values shape our work culture, guiding our interactions and driving our achievements. We are fueled by our commitment to patients and their families, placing their needs at the forefront of our efforts. We embrace authenticity, fostering an environment where every individual feels valued and accepted. Our culture encourages curiosity and the willingness to adapt, as we strive for collective success with urgency, excellence, and purpose. We are unafraid to take risks to unlock innovation and propel scientific advancements; after all, our patients depend on us. These principles are the bedrock of our daily efforts, empowering us to make a meaningful impact. Job OverviewKardigan is in search of an Associate Director of External Manufacturing to lend their expertise in managing a significant late-phase portfolio. This position will report directly to the Senior Director of External Manufacturing.

Role Overview Acadia Pharmaceuticals is hiring an Associate Director of Clinical Operations. This position is based in either Princeton, New Jersey or San Diego, California. The Associate Director will guide key phases of clinical trials, focusing on high-quality execution and adherence to regulatory requirements. What You Will Do Lead and oversee essential stages of clinical trial operations Ensure all activities meet regulatory and company standards Promote effective collaboration across multiple teams Drive project timelines to support company objectives Take a hands-on approach to managing clinical operations

Join Acadia Pharmaceuticals as an Associate Director of Vendor and Relationship Management, where you will play a pivotal role in optimizing our partnerships and vendor strategies. This leadership position requires a vision for fostering strong relationships with our suppliers while ensuring the efficient delivery of our pharmaceuticals.Your main responsibilities will include developing and executing vendor management strategies, overseeing contract negotiations, and ensuring compliance with regulatory standards. You will collaborate with cross-functional teams to support project goals and timelines, contributing to the overall success of Acadia's mission.

About Acadia Pharmaceuticals Acadia Pharmaceuticals is dedicated to transforming scientific potential into innovative solutions that significantly benefit underserved communities dealing with neurological and rare diseases globally. Our current commercial portfolio features the first and only FDA-approved treatments for Parkinson’s disease psychosis and Rett syndrome. We are actively developing a diverse pipeline of therapeutic advancements, which includes mid- to late-stage programs targeting Alzheimer's disease psychosis and Lewy body dementia psychosis, alongside earlier-stage initiatives aimed at addressing various unmet patient needs. At Acadia, our mission is to make a difference in the lives of these patients.Seeking talent near: Princeton, NJPosition SummaryThe Associate Director of Drug Product Development will lead the formulation, primary packaging, and manufacturing process development for Acadia’s expanding portfolio of drug candidates across all development phases. This role involves providing technical oversight, expertise, and guidance for outsourced drug product development activities. The responsibilities encompass the development of formulations, packaging, and processes for various administration routes, including oral solid, liquid, and injectable dosage forms, managing candidates from clinical development through to process validation and lifecycle management. The successful candidate will oversee activities related to these tasks at Contract Service Providers (CSPs) and play a pivotal role in addressing complex technological challenges while implementing new manufacturing technologies for products intended for clinical and commercial distribution. This position is vital for optimizing development, mitigating risks, and expediting the launch of new assets into the market.Primary ResponsibilitiesDesign and develop pharmaceutical formulations and manufacturing processes to support clinical trials, regulatory submissions, and product launches.Evaluate and validate new drug product Contract Service Providers (CSPs) to facilitate development, scaling, and commercialization of new drug candidates within Acadia’s pipeline. Initiate and manage supplier contract agreements as necessary.

Join Kyowa Kirin, a rapidly expanding global specialty pharmaceutical company dedicated to leveraging cutting-edge biotechnologies to develop innovative medicines across four critical therapeutic areas: bone and mineral disorders, intractable hematologic conditions, hematology oncology, and rare diseases. As a Japan-based organization, we strive to transform scientific advancements into life-changing treatments for patients lacking adequate therapeutic options, guiding our projects from drug discovery to development and eventual commercialization. Our North American headquarters is located in Princeton, NJ, with additional offices in California, North Carolina, and Mississauga, Ontario.Position Overview:The Associate Director of Site Budget Management will play a pivotal role in providing strategic and operational direction for designated segments of Kyowa Kirin’s global clinical study portfolio. This position serves as a vital link between study-level execution and overarching enterprise strategies, ensuring effective budget governance, robust forecasting methodologies, financial risk management, and continuous process optimization.In this role, you will ensure budget consistency, oversee negotiation parameters, and manage payment processes while contributing to both short and mid-range portfolio planning. Additionally, you will uphold financial integrity and alignment with global Fair Market Value (FMV) standards across all relevant studies.

Join Acadia Pharmaceuticals Inc. as an Associate Director of Clinical Trial Materials. In this pivotal role, you will oversee the management and delivery of clinical trial materials for our innovative therapies. You will collaborate with cross-functional teams to ensure all materials are prepared and distributed efficiently, ensuring compliance with regulatory standards and timelines.

Join our team as a Part-Time Retail Data Collection Associate and play a crucial role in gathering data that drives key business decisions. You will be responsible for performing in-store audits, collecting product information, and ensuring accurate reporting. This is an exciting opportunity for individuals passionate about retail and data analysis.

Kyowa Kirin is a rapidly expanding global specialty pharmaceutical company leveraging advanced biotechnologies to discover and deliver groundbreaking medicines across four key disease areas: bone and mineral; intractable hematologic; hematology oncology; and rare diseases. Headquartered in Princeton, NJ, with additional offices in California, North Carolina, and Mississauga, Ontario, our mission is to transform scientific innovation into therapeutic solutions where effective treatments are currently lacking.Position Overview:The Associate Director, ERP Functional & Solutions Architect, ICT will play a pivotal role in managing the Microsoft Dynamics 365 (D365) Enterprise Resource Planning (ERP) system within our organization. This position is essential for implementing business process enhancements and ensuring the ERP system operates at peak functionality. The role involves planning, designing, configuring, and customizing MS D365/ERP modules and functionalities, ensuring they integrate seamlessly with existing systems while adhering to industry standards, security protocols, and regulatory requirements. As a business process analyst, the Associate Director will collaborate closely with various corporate functions including Supply Chain Management, Manufacturing, Quality, Finance, Human Resources, Legal, Compliance, and Procurement to ensure the successful development and delivery of technical solutions.Key Responsibilities:The D365 ERP F&O Functional Architect will oversee the comprehensive functional design, configuration, and optimization of Microsoft Dynamics 365 Finance & Operations, supporting business functions across Finance, Procurement, Supply Chain, Manufacturing, and Quality. This role will involve partnering with business stakeholders, technical teams, and implementation partners to align solutions with corporate strategies, ensure compliance with applicable GxP/GAMP 5 standards, and facilitate scalable solutions for future growth.Solution Architecture & Design:Lead the functional design and architecture of the D365 F&O solution across critical modules including Finance, Supply Chain, Manufacturing, Procurement, Inventory, and Quality. Translate complex business requirements into clear, scalable, and compliant functional solutions, emphasizing proactive leadership in solution architecture aligning with business objectives.