Clinical Data Manager

We are seeking a motivated and detail-oriented Clinical Trial Operations Manager I to join our dynamic team. In this pivotal role, you will oversee the operational aspects of clinical trials, ensuring compliance with regulatory requirements and the successful execution of study protocols. Your expertise will contribute to the advancement of innovative therap…

Join our team as a Clinical Trial Operations Manager I, where you will play a crucial role in managing clinical studies, ensuring compliance with regulatory standards, and overseeing the operational aspects of clinical trials. Your expertise will guide the execution of clinical trials from initiation through completion, while collaborating with cross-functional teams to ensure timely delivery and adherence to protocols.

Join our dynamic team as a Clinical Trial Operations Manager III where you will oversee and manage clinical trial operations, ensuring the seamless execution of clinical studies from start to finish. You will collaborate with cross-functional teams to ensure compliance with regulatory standards and drive the successful delivery of trial milestones. This role is perfect for professionals with a strong background in clinical operations, project management, and a passion for improving patient outcomes.

We are seeking an experienced Clinical Trial Operations Manager V to lead our clinical trial operations in Bridgewater, NJ. In this pivotal role, you will oversee the planning, execution, and management of clinical trials while ensuring compliance with regulatory requirements and company policies. You will work closely with cross-functional teams and will be responsible for developing trial strategies, managing budgets, and ensuring timely delivery of trial milestones.

We are seeking a highly skilled and motivated Clinical Project Lead V to join our dynamic team at Artech Information Systems LLC. In this role, you will be responsible for leading and managing clinical projects from initiation through to completion, ensuring adherence to timelines, budgets, and regulatory requirements. Your expertise will be crucial in collaborating with cross-functional teams to drive successful project outcomes.

We are seeking a highly motivated and detail-oriented Clinical Project Assistant IV to join our dynamic team. In this role, you will support clinical project managers in the execution of clinical trials and ensure compliance with regulatory requirements. This position is ideal for someone with a strong organizational skill set and a passion for the clinical research field.

We are seeking a skilled and experienced Clinical Study Director to lead and manage clinical trials within our organization. The ideal candidate will possess a deep understanding of clinical research processes, regulatory requirements, and the ability to coordinate with cross-functional teams.As a Clinical Study Director, you will play a pivotal role in the design, implementation, and oversight of clinical studies. You will be responsible for ensuring that studies are conducted in compliance with Good Clinical Practice (GCP) and applicable regulations.

Join our dynamic team as a Clinical Project Publishing Manager at Artech Information Systems LLC, where your expertise will drive the success of critical clinical projects. In this role, you will oversee the publication processes, ensuring that all project deliverables meet the highest standards of quality and compliance. You will collaborate closely with cross-functional teams to facilitate seamless communication and project execution.

We are seeking a dedicated and detail-oriented Clinical Project Lead to join our dynamic team. In this pivotal role, you will oversee clinical projects from inception to completion, ensuring that all activities are executed in compliance with regulatory requirements and industry standards. Your leadership will help drive project success, fostering collaboration among cross-functional teams and maintaining clear communication with stakeholders.

Join dstaff as a Digital Operations Manager and lead our digital initiatives to new heights. In this pivotal role, you will oversee the execution of digital projects, ensuring alignment with business goals while enhancing operational efficiency. You will collaborate with cross-functional teams to develop innovative strategies that optimize our digital presence and drive results.

Join Cellares as a strategic and innovative Director of Operations Finance. We are looking for a highly motivated leader with profound expertise in Financial Planning & Analysis (FP&A), accounting, manufacturing, supply chain management, and business collaboration. Your proven track record will be instrumental in propelling our organization toward achieving our ambitious objectives.In this pivotal role, you will provide essential support to our global Operations organization, including our manufacturing facilities in Bridgewater, NJ, Europe, and Japan. Your responsibilities will encompass product costing and enhancing operational efficiencies to boost gross margins. Additionally, you will spearhead the cost forecasting process for assets in development and new products within the commercial pipeline. You will lead finance teams across our worldwide manufacturing sites.Ideal candidates will possess intellectual curiosity, meticulous attention to detail, and a collaborative spirit to devise solutions for intricate challenges. This hands-on role in a rapidly scaling early-stage company demands the ability to drive organizational performance through insightful financial analysis and foresight, which is critical to our success.We seek individuals who thrive in a fast-paced, mission-driven environment and are ready to confront a diverse range of challenges as our company continues to grow.

We are seeking a dedicated and analytical Operations Research Engineer to join our dynamic team. This role is essential for optimizing our operational processes and enhancing decision-making through data-driven analysis. As an Operations Research Engineer, you will work on developing models and algorithms to solve complex logistical problems, ensuring that our operations run smoothly and efficiently.

Cellares is on the lookout for a dynamic and driven Senior Director of Supply Chain Management to report directly to our VP of Operations. In this pivotal role, you will spearhead the development and execution of a robust Supply Chain strategy that aligns with our organizational goals and meets the demands of both internal and external stakeholders. Your responsibilities will encompass a wide range of supply chain functions, including patient supply and material planning, materials management, inventory control, product tracking (including chain of identity and chain of custody), import/export permits, shipping and receiving logistics, as well as maintaining cold chain logistics for personalized cell therapies across our manufacturing network. This role requires a versatile leader capable of fostering effective communication and collaboration across various cross-functional teams, including Manufacturing, Quality, MS&T, QC, Process/Analytical Development, Training, Engineering/Facilities, HS&E, Finance, IT, and Commercial Sales. The ideal candidate will thrive in a fast-paced, mission-driven environment and be eager to tackle a diverse array of challenges that will arise as our company continues to grow.

The Operations Lead at Alo Yoga in Bridgewater, NJ ensures daily store functions run smoothly while supporting the company’s commitment to wellness and mindfulness. This role is central to maintaining a positive in-store experience and efficient operations. Main responsibilities Manage daily store operations, ensuring all tasks and processes are completed on schedule Identify and implement ways to improve efficiency and customer service Guide and support team members to achieve business objectives Location This position is based in Bridgewater, New Jersey, United States.

Position OverviewCellares is on the lookout for a dynamic and driven Manufacturing Supervisor to lead our Cell Therapy Operations team. This pivotal role involves the ramp-up and management of cGMP operations within our cutting-edge multi-product cell therapy manufacturing facility, dedicated to producing both autologous and allogeneic cell therapy products. The successful candidate will collaborate closely with various departments to ensure the safe and compliant manufacturing of cell therapy products in accordance with cGMP standards. This role demands strong leadership to facilitate effective communication, coordination, and teamwork across diverse functional areas, ensuring smooth production processes, thorough testing, and timely product release for patients.As a multidisciplinary role, the Manufacturing Supervisor will interface with all levels of the organization, including Manufacturing, Quality, MSAT, QC, Process/Analytical Development, Supply Chain, Warehouse, Training, Engineering/Facilities, and EH&S. We are seeking a candidate who thrives in a fast-paced, mission-driven environment and is ready to embrace a wide range of challenges as the company continues to expand.

Join our dynamic team at JYSK Canada as an Assistant Manager. In this pivotal role, you'll support the Store Manager in daily operations, drive sales performance, and ensure exceptional customer service. Your leadership will inspire the team to reach their full potential, creating an engaging shopping experience for our customers.

We are seeking a highly skilled and experienced Project Manager V to join our dynamic team. In this role, you will be responsible for overseeing complex projects from inception to completion. You will work closely with stakeholders to ensure project goals are met on time and within budget. Your leadership and expertise will be vital in driving project success while fostering a collaborative and innovative environment.

We are seeking a dedicated Quality Engineer I to join our team in Bridgewater, NJ. In this role, you will play a crucial part in ensuring the quality and reliability of our products. You will work collaboratively with cross-functional teams to develop and implement testing strategies and quality assurance processes.If you are passionate about quality engineering and eager to contribute to innovative projects, we would love to hear from you!

We are looking for a talented Automation Engineer to enhance the development, validation, and daily operation of fully automated Quality Control (QC) testing workflows within a regulated GMP environment at our Bridgewater, NJ facility. This position is pivotal to the success of our Cell Q platform and our commercial-scale QC operations.The ideal candidate will be instrumental in the transfer, scaling, and optimization of automated QC test methods across various automated workcells. The role also involves providing hands-on operational support for the Cell Q platform and the wider QC laboratory setup. Responsibilities include troubleshooting systems, assisting with production testing, and ensuring the consistent and compliant execution of automated workflows.Collaborating closely with cross-functional teams in Quality Control, Analytical Development, Manufacturing, IT, and Quality, the Automation Engineer will contribute to system validation, user training, technical documentation, and the controlled version management of automated test methods under change control. Additionally, this role will be involved in designing, implementing, and maintaining automated sample and reagent management workflows to facilitate scalable, reliable, and robust end-to-end processes for high-throughput QC testing in a GMP setting.We seek candidates who thrive in a fast-paced, mission-driven environment and are eager to tackle a diverse array of challenges as our company continues to grow.