Clinical Contracts Specialist

At Iterative Health, we are at the forefront of healthcare technology and services, dedicated to revolutionizing clinical research and enhancing patient outcomes. Our Site Network is a distinguished consortium of over 70 clinical research sites across the United States and Europe, accelerating the introduction of innovative therapies in gastrointestinal (GI) and hepatology. We focus on empowering our partner sites with technology-driven services, combining extensive clinical trial expertise with cutting-edge artificial intelligence (AI), enabling research teams and sponsors to broaden and hasten access to essential therapeutics for patients.We are pioneering the integration of advanced, proprietary AI tools in cardiology and drug development, aiming to significantly enhance clinical decision-making while improving patient lives through superior diagnosis, disease management, and treatment.As a Senior Clinical Research Specialist I, you will report to the Head of Cardiology and Growth, collaborating closely with the Director of Clinical Research (Cardiology) to integrate Iterative Health’s services and AI solutions at cardiology-focused clinical research sites nationwide. This role requires exceptional communication skills, customer engagement, and comprehensive clinical research expertise, coupled with a robust strategic skill set. You will directly support a portfolio of sites by assessing their current state using our established methodologies, delivering tailored training and ongoing assistance to promote research best practices, drive the adoption of Iterative Health’s services, and ensure that our sites meet their research objectives.

Iterative Health is at the forefront of healthcare technology and services, dedicated to expediting clinical research to enhance patient outcomes. With a robust Site Network comprising over 70 clinical research sites across the United States and Europe, we specialize in accelerating the journey to market for innovative therapies in gastrointestinal (GI) and hepatology. Our mission is to foster the growth and success of our partner sites by equipping them with advanced technology-driven services. By merging extensive clinical trial expertise with pioneering AI solutions, we empower research teams and study sponsors to broaden and hasten access to crucial novel therapeutics for patients in need.About the RoleWe are on the lookout for a proactive and detail-oriented Clinical Research Finance Specialist to become a vital member of our expanding Finance team. This role entails close collaboration with the Finance Manager to oversee comprehensive accounts receivable operations related to sponsor-funded clinical studies and internal research sites.As a key player, you will manage essential transactional accounts receivable workflows, including monitoring sponsor and site-level accounts, facilitating timely collections, posting cash in RealTime CTMS, and providing invoicing support as necessary. This position demands strong collaboration with internal teams, research sites, and sponsors and CROs to guarantee precise billing, timely cash application, and swift resolution of outstanding balances.The ideal candidate will thrive in a dynamic clinical research environment, adeptly balancing hands-on execution with cross-functional teamwork and a commitment to continuous process enhancement.Key ResponsibilitiesManage daily accounts receivable operations, including monitoring sponsor and site-level balances and aiding in timely collections.Reconcile study-level balances and payment activities, identifying discrepancies and collaborating with stakeholders to resolve issues.Accurately record cash receipts and payment details in RealTime CTMS and related financial systems.Prepare and dispatch invoices for study activities and services in coordination with sponsor communications and internal teams.Professionally communicate with sponsors and CROs regarding billing inquiries, payment statuses, and outstanding balances.Assist in generating AR aging schedules, financial summaries, and internal reports.Support audits and financial reviews pertaining to accounts receivable and billing activity.Work collaboratively with Clinical Operations, Site Finance, and Accounting to clarify billing terms and deliverables.Contribute to ongoing process improvements to boost accounts receivable efficiency, accuracy, and visibility.

Iterative Health is seeking a Clinical Research Systems Specialist to help advance clinical research operations by supporting and maintaining system solutions. This position plays a key role in ensuring that clinical research management systems run smoothly and meet the needs of various teams across the organization. What you will do Work with cross-functional teams to address clinical research system requirements Implement new clinical research management systems and handle ongoing maintenance Support data integrity and compliance throughout all research activities Location This role is based in either Cambridge, Massachusetts or New York, New York.

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.

Join eGenesis as a Senior Clinical Research AssociateAt eGenesis, we are at the forefront of innovation in biotechnology, developing human-compatible engineered organs to combat the critical global organ shortage. Our cutting-edge genome engineering platform allows for extensive gene modifications, effectively removing biological barriers and introducing protective human transgenes. Our leading program, EGEN-2784, involves a genetically engineered porcine kidney currently under a multi-patient Expanded Access study at Massachusetts General Hospital (MGH). We are proudly headquartered in Cambridge, MA, and are dedicated to making a significant impact on healthcare.We are currently in search of a highly skilled Senior Clinical Research Associate with over 4 years of experience in monitoring intricate clinical trials within pharmaceutical, biotechnology, and CRO settings. The ideal candidate will demonstrate proven expertise in managing investigative sites, conducting site qualifications, initiation, routine monitoring (both on-site and remote), and closeout visits while ensuring adherence to ICH-GCP, regulatory requirements, and study protocols. You will be tasked with overseeing site performance, preserving data integrity through source data verification and CRF review, and maintaining timely documentation in eTMF, CTMS, and EDC systems. Additionally, you will support site start-up activities, provide training for investigators and site staff, and offer operational guidance to academic medical centers, particularly those with limited IND experience. The right candidate will possess strong capabilities in identifying operational risks, implementing effective mitigation strategies, and managing high volumes of clinical data to uphold patient safety, data quality, and study compliance. Reporting to the Lead CRA or Clinical Operations leadership, you will execute monitoring strategies and facilitate consistent oversight of assigned sites. We value collaboration and are looking for a team player who can work closely with investigative sites and cross-functional teams to enhance enrollment, address operational challenges, and ensure inspection readiness.

We are seeking a dedicated and experienced Senior Clinical Study Manager to join our dynamic team in Cambridge. In this role, you will oversee the planning and execution of clinical studies, ensuring they meet regulatory standards and are completed on time and within budget. You will lead cross-functional teams and collaborate with various stakeholders to drive project success.The ideal candidate will have a proven track record in managing clinical trials, excellent communication skills, and the ability to navigate complex challenges. If you are passionate about advancing clinical research and want to make a significant impact, we encourage you to apply.

About eGenesiseGenesis is an innovative clinical-stage biotechnology company dedicated to developing human-compatible engineered organs to tackle the critical global organ shortage. Our proprietary genome engineering platform facilitates extensive, multiplex gene edits aimed at removing major biological barriers, incorporating protective human transgenes, and inactivating endogenous retroviruses. Our flagship program, EGEN-2784, a genetically engineered porcine kidney, is currently undergoing evaluation in a multi-patient Expanded Access study at Massachusetts General Hospital (MGH). Headquartered in the vibrant city of Cambridge, MA, eGenesis is at the forefront of pioneering medical solutions.As the Lead Clinical Research Associate, you will spearhead site monitoring activities and oversee Clinical Research Associates (CRAs) for designated clinical trials. Collaborating closely with Clinical Operations leadership and cross-functional teams, you will ensure that studies are executed in strict adherence to protocols, ICH-GCP guidelines, regulatory requirements, and our company Standard Operating Procedures (SOPs).

Scholar Rock is a pioneering biopharmaceutical company dedicated to the discovery, development, and delivery of transformative therapies for patients suffering from serious diseases with significant unmet medical needs. As a global frontrunner in the understanding of the transforming growth factor beta (TGFβ) superfamily of cell proteins, Scholar Rock is aptly named for the visual resemblance of a scholar rock to protein structures. The company is currently in the clinical stage, focusing on advancing groundbreaking treatments that leverage protein growth factors to create better health outcomes. Over the past decade, Scholar Rock has cultivated a robust pipeline aimed at improving the standard of care for conditions such as neuromuscular diseases, cardiometabolic disorders, cancer, and other areas where growth factor-targeted therapies could effectuate significant change. Scholar Rock stands out as the sole company to demonstrate clinical proof of concept for a muscle-targeted treatment for spinal muscular atrophy (SMA). We are committed to pioneering fundamentally different therapeutic approaches, supported by our proprietary platform that has developed novel monoclonal antibodies capable of exquisitely modulating protein growth factors. By utilizing cutting-edge scientific advancements in disease areas that have been historically underserved by conventional therapies, Scholar Rock is dedicated to unlocking new possibilities for patients. To learn more about our innovative approach, visit ScholarRock.com and follow us on @ScholarRock and LinkedIn.Position Overview:The Medical Director/Senior Director will report directly to the Senior Vice President of Clinical Research and will play a crucial role within the late-stage development team. This individual will be responsible for overseeing the clinical development activities for product candidates, guiding them from Proof-of-Concept through to marketing approval and ongoing lifecycle management. The ideal candidate will provide medical leadership for the clinical development of apitegromab and other late-stage product candidates in accordance with the overall corporate strategy. This role requires an enthusiastic physician-scientist with substantial hands-on experience in advancing late-stage product candidates to deliver revolutionary therapies.

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.

Join Iterative Health, a pioneering healthcare technology and services company dedicated to accelerating clinical research and transforming patient outcomes. With a robust network of over 70 clinical research sites across the US and Europe, we are at the forefront of advancing novel therapies in gastrointestinal (GI) and hepatology. Our mission is to enhance the success and growth of our partner sites through innovative tech-enabled services. By leveraging deep clinical trial expertise and advanced AI, we empower research teams and sponsors to broaden access to life-changing therapeutics for patients in need.Position Location: HybridAs the Senior Manager of Clinical Operations, you will play a critical role in reporting to the Director of Clinical Operations and collaborating closely with our Clinical Research and Life Science teams. Your key responsibilities will include engaging with partners such as sponsors, CROs, and key sites to drive operational alignment. You will provide strategic recommendations aimed at improving research operations, engaging with sponsors and CROs to report on study progress from site selection to closeout. You will also be responsible for optimizing study performance by assessing gaps, prioritizing service implementation, and serving as a subject matter expert.This is a vital, customer-facing role, where you will deliver clinical research best practices and thought leadership to our sites and sponsors.

We are seeking a highly motivated and experienced Senior Clinical Study Manager to lead and oversee clinical trials in our innovative organization. In this pivotal role, you will manage the planning, execution, and reporting of clinical studies, ensuring compliance with regulatory requirements and adherence to timelines.The ideal candidate will possess a strong background in clinical research, with proven experience in managing complex clinical operations. You will collaborate closely with cross-functional teams, including clinical operations, data management, and regulatory affairs, to drive the success of our clinical programs.

As a Senior Associate for Clinical Trial Transparency at Integrated Resources, Inc., you will play a pivotal role in ensuring the integrity and transparency of clinical trial data. This position involves collaborating with clinical teams to develop and implement strategies that align with regulatory requirements and promote public trust in clinical research. You will leverage your expertise to maintain compliance and enhance the visibility of our clinical trials.

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.

Join our dynamic team as a Clinical Trial Leader, where you will be at the forefront of innovative clinical research. You will be responsible for overseeing the planning, execution, and management of clinical trials, ensuring compliance with all regulatory requirements and organizational standards. Your leadership will guide cross-functional teams to deliver high-quality results, contributing to the advancement of healthcare solutions.

Join Integrated Resources Inc. as a Clinical Study Manager and play a pivotal role in driving groundbreaking clinical research initiatives. We are looking for a dynamic professional who excels in managing clinical trials, ensuring compliance with regulatory standards, and optimizing study protocols.Your expertise will be integral to our mission of advancing healthcare solutions and improving patient outcomes. If you're passionate about clinical research and want to make a significant impact in the industry, we encourage you to apply.

We are seeking a highly motivated Senior Research Associate to join our dynamic team at Integrated Resources, Inc. In this pivotal role, you will conduct advanced research, analyze data, and contribute to innovative projects that drive our mission forward. If you are passionate about scientific research and eager to make an impact, we want to hear from you!

We are seeking a talented and dedicated Senior Research Associate to join our dynamic team in Cambridge. In this role, you will contribute to innovative research projects and collaborate with interdisciplinary teams to drive impactful findings.

We are seeking a dedicated and detail-oriented Clinical Study Manager to oversee the planning, execution, and management of clinical studies. This role is pivotal in ensuring adherence to regulatory requirements, study protocols, and timelines. The ideal candidate will lead cross-functional teams, manage budgets, and maintain communication with stakeholders to drive the success of clinical trials.

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.