Clinical Data and Analytics Lead

At Iterative Health, we are at the forefront of healthcare technology, revolutionizing clinical research to enhance patient outcomes. Our Site Network comprises over 70 top-tier clinical research sites across the US and Europe, focusing on advancing gastrointestinal (GI) and hepatology therapies. We empower our partner sites with innovative, technology-driven services, combining extensive clinical trial expertise with advanced AI solutions. Our mission is to facilitate swift access to groundbreaking therapeutics for patients in need, thereby improving lives and health outcomes.The Clinical Data Specialist plays a pivotal role in our clinical trial service operations, primarily responsible for conducting electronic health record (EHR) reviews to identify eligible patients for clinical trials.

At Iterative Health, we are at the forefront of healthcare technology, dedicated to revolutionizing clinical research and improving patient outcomes. With a robust network of over 70 clinical research sites across the US and Europe, we expedite the journey to market for innovative gastrointestinal (GI) and hepatology therapies. Our mission is to empower our partner sites with advanced, tech-enabled services, merging extensive clinical trial expertise with state-of-the-art AI solutions, allowing research teams and study sponsors to broaden and hasten access to groundbreaking therapeutics.As a pioneering organization in applying powerful proprietary AI tools within gastroenterology, cardiology, and drug development, we aim to significantly enhance clinical decision-making, thereby improving patient lives through superior diagnostics, disease management, and treatment approaches that lead to better health outcomes.The Clinical Data Specialist plays a crucial role in our clinical trial service operations by conducting EHR chart reviews to identify suitable candidates for clinical trials.

As a Clinical Site Relationship Manager, you will play a pivotal role in fostering strong partnerships with clinical sites, ensuring seamless operations and enhancing the overall clinical trial experience. Your expertise will be vital in managing site relationships, providing support, and facilitating communication between stakeholders to achieve successful trial outcomes.

We are seeking a dedicated and experienced Clinical Operations Lead to oversee and enhance our clinical operations. In this pivotal role, you will be responsible for ensuring that our clinical trials are executed efficiently and in compliance with regulatory standards. You will collaborate closely with cross-functional teams to streamline processes, improve patient care, and deliver high-quality results.

Join Integrated Resources Inc. as a Clinical Data and Analytics Lead, where your expertise will drive innovative solutions in clinical research. In this pivotal role, you will oversee the management and analysis of clinical data, ensuring accuracy and compliance with regulatory standards. Collaborate with cross-functional teams to enhance data quality and deliver actionable insights that support clinical decision-making.

Join our dynamic team as a Clinical Data Manager, where you will play a pivotal role in managing and overseeing clinical data processes. Your expertise will contribute to the integrity and accuracy of clinical trials, ensuring data quality and compliance with regulatory standards.

Iterative Health is a pioneering healthcare technology and services company dedicated to revolutionizing clinical research and enhancing patient outcomes. With an extensive network of over 70 clinical research sites in the U.S. and Europe, we are at the forefront of accelerating the market introduction of innovative gastrointestinal (GI) and hepatology therapies. Our mission is to empower our partner sites through advanced tech-enabled services, leveraging our deep expertise in clinical trials and state-of-the-art AI to broaden access to groundbreaking therapeutics for patients in need.About the RoleThe Regional Director will lead and enhance the performance of GI-focused clinical research sites within their portfolio. This role is crucial in ensuring operational excellence, aligning teams to achieve key performance metrics, elevating site capabilities, and maintaining consistency in trial execution. As a strategic leader in operations, the Regional Director will bridge site performance with overarching business objectives.ResponsibilitiesOversee staff across multiple sites, ensuring alignment with protocols, regulatory standards, and Iterative Health's guidelines.Take full ownership of site performance, encompassing recruitment, data integrity, compliance, and team culture.Ensure sites are optimally prepared for success through adequate staffing, equipment, and training, providing recommendations for resource allocation based on business needs.Foster strong partnerships with Principal Investigators (PIs) to align their engagement with study objectives and operational strategies.Influence the study portfolio to enhance profitability and patient value.Proactively identify and address issues related to site performance.Guide and develop Clinical Research Coordinators (CRCs) and site-based research personnel through clear expectations, performance coaching, and team development.Act as a visible and hands-on leader, cultivating high-performing, accountable teams.Analyze KPIs and monitor performance trends to identify and leverage factors driving site-level success.Implement corrective actions and process enhancements as necessary.Serve as the primary operational liaison between site personnel and central functions.Promote a culture of accountability, collaboration, and continuous improvement throughout all assigned sites.

We are seeking a highly skilled Senior Clinical Operations Lead to join our dynamic team at Integrated Resources Inc. In this pivotal role, you will oversee clinical operations, ensuring that all processes align with regulatory standards and best practices. Your expertise will guide the planning, execution, and management of clinical trials, fostering collaboration across multidisciplinary teams.The ideal candidate will have a strong background in clinical research and operations, with a proven track record of leading successful clinical projects. You will be instrumental in optimizing operational efficiency and driving the success of our clinical programs.

Join our dynamic team as a Clinical Data Entry Coordinator at Mindlance in Cambridge, MA. In this pivotal role, you will be responsible for accurately inputting and managing clinical trial data to support our ongoing research initiatives.

We are seeking an experienced Clinical Trial Operations Manager to lead and oversee clinical trial activities at Artech Information Systems LLC. In this role, you will be responsible for managing the operational aspects of clinical trials, ensuring compliance with regulatory requirements, and collaborating with cross-functional teams to deliver high-quality results. Your expertise will contribute to the advancement of innovative solutions in the clinical research field.

We are seeking a highly skilled Clinical Operations Lead to join our dynamic team. In this pivotal role, you will oversee the management of clinical operations to ensure efficient execution of clinical studies. Your expertise will be instrumental in driving the strategic direction of our clinical programs and leading cross-functional teams to achieve project objectives.

We are seeking a highly skilled and motivated Clinical Operations Lead to oversee our clinical trials and operations. The ideal candidate will possess extensive knowledge of clinical research processes, ensuring that our studies are conducted efficiently and in compliance with regulatory standards. You will play a pivotal role in managing trial execution, coordinating teams, and optimizing operational strategies to drive successful outcomes.

Join our team as a Clinical Safety Data Manager, where you will play a pivotal role in ensuring the safety and efficacy of our clinical trials. You will manage safety data, conduct thorough analyses, and collaborate closely with cross-functional teams to maintain the highest standards of patient safety.

Join our dynamic team at Integrated Resources, Inc. as a Clinical Safety Data Manager. In this pivotal role, you will oversee the management and analysis of clinical safety data, ensuring compliance with regulatory standards and enhancing patient safety. Your expertise will be vital in developing safety databases and implementing data management processes that support clinical trials.

We are seeking a highly skilled and experienced Senior Clinical Operations Lead to join our dynamic team in Cambridge. As a pivotal member of our clinical operations team, you will play a critical role in overseeing the planning, execution, and management of clinical trials. Your expertise will ensure adherence to regulatory standards and best practices, while also fostering collaboration across multidisciplinary teams.Your responsibilities will include developing operational strategies, managing budgets, and ensuring timely project delivery. You will also be responsible for mentoring junior staff and facilitating training programs.

Integrated Resources Inc. is seeking an experienced Clinical Operations Lead to join our dynamic team in Cambridge, Massachusetts. This pivotal role involves overseeing clinical trial operations, ensuring compliance with regulatory standards, and leading cross-functional teams to achieve project milestones. The ideal candidate will have a strong background in clinical research and a passion for advancing healthcare solutions.

Iterative Health is a leading healthcare technology and services firm dedicated to enhancing the pace of clinical research aimed at improving patient outcomes. Our Site Network comprises over 70 top-tier clinical research sites across the United States and Europe, focused on accelerating the market entry of innovative therapies in gastrointestinal (GI) and hepatology. Our mission is to ensure the success and growth of our partner sites through advanced tech-enabled services. By merging extensive clinical trial expertise with state-of-the-art AI, we empower research teams and study sponsors to broaden and hasten access to novel therapeutics for patients in need.About the RoleWe are in search of a motivated and detail-oriented Clinical Contracts Specialist to join our dynamic Legal team. In this pivotal role, you will be responsible for managing and negotiating clinical trial agreements with sponsors and biotechnology partners, serving as a vital point of contact throughout the contract lifecycle. Your organizational and communication skills, along with your commitment, will significantly influence the success of our clinical partnerships and the patients we serve.

We are seeking a highly skilled and motivated Contract Clinical Operations Lead to join our dynamic team. In this pivotal role, you will oversee clinical trial operations, ensuring adherence to regulatory requirements and best practices. Your expertise will guide project management, resource allocation, and team coordination, driving the successful execution of clinical studies.

Join Integrated Resources Inc. as a Clinical Operations Lead, where you will play a pivotal role in overseeing clinical trials and operations. You will be responsible for ensuring compliance, managing timelines, and leading a team of professionals dedicated to advancing healthcare solutions. Your expertise will help streamline processes and improve patient outcomes.