Clinical Data Manager

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 our team as a Data Collection Specialist and play a vital role in gathering and analyzing critical data that drives our business decisions. This part-time position is perfect for individuals looking to kickstart their career in data management and analysis.

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 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.

We are seeking a talented and driven Clinical Data and Analytics Lead to join our dynamic team in Cambridge, MA. This role will be pivotal in overseeing the collection, management, and analysis of clinical data to ensure the highest quality of insights and analytics. You will collaborate with cross-functional teams to develop data solutions that drive strategic decisions and improve patient outcomes.The ideal candidate will have a strong background in clinical data management, proven analytical skills, and a passion for leveraging data to enhance healthcare delivery. If you are ready to make a significant impact in the field of clinical analytics, we want to hear from you!

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.

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.

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.

Join Integrated Resources, Inc. as a Clinical Trials Safety Data Manager, where you will play a crucial role in ensuring the safety and efficacy of clinical trials. In this dynamic position, you will oversee data management processes, ensuring the integrity and accuracy of safety data collected during trials.We are seeking a detail-oriented professional with a strong background in clinical data management and an understanding of regulatory requirements related to clinical trials. You will collaborate with cross-functional teams to support our mission of advancing medical research and improving patient outcomes.

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.

Join our team as a Part-Time Retail Data Collection Associate and play a vital role in gathering and analyzing retail data that drives decision-making in the industry. This position offers flexible hours, allowing you to work at your convenience while contributing to important retail insights.

Join our dynamic team as a Part-Time Retail Data Collection Associate where you will play a crucial role in gathering valuable retail insights. This position is perfect for individuals who enjoy engaging with products and have a keen eye for detail. As a part of our team, you will conduct data collection in various retail environments, ensuring accuracy and reliability in reporting.

As a Part-Time Retail Data Collection Associate, you will play a crucial role in gathering and analyzing retail data to support our clients. This position offers flexible hours, allowing you to balance work with other commitments. Ideal candidates will have a keen eye for detail and possess strong analytical skills.

Join a dynamic team as a Part-Time Retail Data Collection Associate in Cambridge, where you will play a vital role in gathering essential data that drives retail decisions. Your responsibilities will include conducting in-store visits, collecting data, and ensuring the accuracy of information for our retail partners.This position is ideal for individuals who are detail-oriented and enjoy working independently. If you're looking to contribute to a growing company and make a real impact, we want to hear from you!

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.

Amylyx Pharmaceuticals is on a bold mission to revolutionize the treatment of diseases that have significant unmet needs. While others may see obstacles, we actively pursue opportunities with urgency, rigorous scientific methods, and a steadfast commitment to the communities we serve. As a clinical-stage company, we are currently targeting conditions such as post-bariatric hypoglycemia (PBH), Wolfram syndrome, and amyotrophic lateral sclerosis (ALS).Our mission is driven by our talented team, united by core values that include being audacious, curious, authentic, engaged, and accountable, fostering a culture of compassion. At Amylyx, we have assembled a highly experienced group dedicated to action, as the communities we serve cannot afford to wait. If you share our passion and are committed to addressing some of the most challenging problems in medicine, we invite you to explore this opportunity and apply.The OpportunityThe Clinical Data Management team at Amylyx Pharmaceuticals is in search of an Associate Director, Clinical Data Programmer. In this role, you will collaborate across functions to deliver hands-on data management support, programming expertise, and technical leadership. You will be responsible for developing, maintaining, and validating clinical databases, as well as executing computer programs to access, visualize, and report clinical trial data, adhering to clinical plans, ICH guidelines, and regulatory standards. As the Associate Director of Clinical Data Programming, proficiency in programming languages is essential for creating both textual and graphical representations that facilitate data cleaning and review.

Join our dynamic team at Crossmark as a Part-Time Retail Data Collection Associate. In this role, you will be responsible for gathering and reporting essential data from retail environments. Your insights will help shape the future of retail strategies and enhance customer experiences. This position offers flexible hours and the chance to work with a team dedicated to excellence.

Join our dynamic team as a Part-Time Retail Data Collection Associate where you will play a crucial role in shaping market insights by collecting and analyzing retail data. This position enables you to work flexibly while contributing to meaningful projects that influence product availability and merchandising strategies.