Data Quality Analyst

Join Integrated Resources, Inc. as a Data Management Quality Associate, where you will play a crucial role in ensuring the integrity and quality of our data management processes. You will collaborate with cross-functional teams to enhance data accuracy and streamline operations.

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 Integrated Resources Inc. as a Quality Assurance Documentation Associate! In this pivotal role, you will be responsible for ensuring the accuracy and quality of our documentation processes. Your keen attention to detail and commitment to excellence will help us maintain high standards in our quality assurance practices.

We are seeking a proactive and detail-oriented Data Management Vendor Manager Associate to join our dynamic team. In this role, you will be responsible for overseeing vendor relationships and ensuring seamless data management processes. Your contributions will be essential in fostering collaboration and optimizing performance across various projects.

We are seeking a dedicated and detail-oriented Quality Control Manager to join our dynamic team at Integrated Resources Inc. in Cambridge, Massachusetts. The ideal candidate will be responsible for ensuring the highest standards of quality across our products and services, implementing rigorous quality management systems, and leading a team of quality assurance professionals.As a Quality Control Manager, you will play a crucial role in driving continuous improvement initiatives and collaborating with cross-functional teams to enhance operational efficiency. Your expertise will help us maintain compliance with industry regulations and exceed customer expectations.

Amylyx Pharmaceuticals is dedicated to revolutionizing the treatment of diseases with significant unmet needs. We embrace challenges as opportunities, driven by a sense of urgency, rigorous scientific methodology, and a steadfast commitment to the communities we serve. Our focus is on clinical-stage development for conditions such as post-bariatric hypoglycemia (PBH), Wolfram syndrome, and amyotrophic lateral sclerosis (ALS).Our mission thrives on our talented team, which embodies core values of audacity, curiosity, authenticity, engagement, and accountability — all of which foster a culture of care. Amylyx has curated a skilled workforce ready to act swiftly because the communities we support cannot afford to wait. If you are passionate about addressing some of the most challenging issues in medicine, we invite you to explore the opportunity below and apply.The OpportunityThe Associate Director of Computer System Validation (CSV) & Quality Compliance will provide enterprise-level leadership, strategic direction, and governance for the validation, lifecycle management, and continuous compliance of GxP-relevant computerized systems, particularly focusing on the Veeva Quality Suite. This position is pivotal in ensuring that our digital quality solutions and supporting systems comply with global regulatory standards (FDA, EMA, ICH, GAMP 5), safeguard data integrity, and maintain a sustainable, inspection-ready status across the organization.This role entails close collaboration with Quality, IT, Regulatory, Clinical, and business process owners to define system requirements, oversee new system implementations and significant enhancements, and promote harmonized, risk-based validation practices. Additionally, this position supervises quality compliance processes such as Change Control, Deviations, CAPA, and continuous improvement, ensuring timely resolutions, trend analysis, and effective governance through leadership of key forums, including Quality Management Review and cross-functional compliance meetings.

The Associate Director of Data Strategy and Governance is responsible for spearheading the University’s data governance initiatives. This role collaborates with senior leaders and data stewards to cultivate a data-driven culture, enhancing best practices in metadata management, data quality, and data security. This position plays a crucial role in elevating Harvard’s overall data maturity.Reporting to the Associate Provost for Institutional Research & Analytics and working closely with the AVP for Administrative Technology Services in HUIT, the Associate Director will coordinate efforts with both OIRA and HUIT to meet the data needs of the entire University.Key Responsibilities:This role is integral in uniting stakeholders across the University to address pressing data-related challenges, while establishing mechanisms to safeguard and strategically utilize our data. As the University’s data maturity progresses, the responsibilities of the Associate Director may adapt accordingly.Organizational Development & Communications:Lead and recruit members for the Executive Data Committee (EDC), University Data Advisory Group (UDAG), and Data Stewardship Council (DSC).Establish effective communication channels regarding data initiatives across various schools and departments and build a thriving community of practice among data stewards.Develop and sustain a curriculum for data governance training for data stewards and other key stakeholders.Enhance executive support for data governance initiatives throughout the University.Deliver strategic updates on data initiatives to various University stakeholders.Engage in thought leadership discussions and forums on data strategy and governance in higher education.Data Strategy Development:Collaborate in creating an enterprise data strategy for the University, taking the lead on project management to track progress toward its goals.Facilitate the identification, development, and promotion of strategic data initiatives.Data Governance Execution:Establish data governance standards, policies, procedures, and best practices, and create a framework to disseminate these practices among stakeholder groups.Improve the University’s management of metadata (e.g., data definitions, data lineage) across diverse data sources.Collaborate with the Information Security and Data Privacy (ISDP) team on data security and privacy efforts, ensuring compliance with regulations.

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!

Join Nuvalent as a Manager in GMP Quality Assurance, where you will play a pivotal role in ensuring the highest quality standards in our manufacturing processes. You will lead a dynamic team, working collaboratively to uphold compliance with regulatory requirements and internal protocols. Your expertise will contribute to our mission of delivering innovative therapies to patients.

We are seeking a highly skilled and experienced Director of Clinical Quality to join our dynamic team at Integrated Resources, Inc. In this pivotal role, you will be responsible for overseeing the clinical quality management systems, ensuring compliance with regulatory standards, and driving continuous improvement in clinical processes.Your leadership will be vital in fostering a culture of quality and safety, collaborating with multidisciplinary teams to enhance patient outcomes and operational efficiency.

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.

Join Harvard University as a Data Analytics Manager and lead the charge in transforming data into actionable insights. In this pivotal role, you will oversee a dynamic team, driving innovative analytics solutions that support strategic decision-making across the university. Your expertise will be essential in harnessing data to enhance operational efficiency and improve student outcomes.

Join our dynamic team as a Quality Control Analyst II, where you will play a vital role in ensuring the highest standards of quality in our products. This position is ideal for detail-oriented individuals who are passionate about quality assurance and eager to contribute to the success of our projects.

Join our dynamic team as a Quality Assurance/Quality Control Specialist III. In this pivotal role, you will ensure the highest quality standards are maintained throughout our processes and products. As a QA/QC Specialist, you will be responsible for developing and implementing quality assurance programs, conducting audits, and collaborating with cross-functional teams to drive continuous improvement.

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.

Join Harvard University as a Finance and Data Manager, where you will play a crucial role in overseeing financial operations and data management. In this dynamic position, you will collaborate with various departments to ensure accuracy in financial reporting and data analytics.

We are seeking a dedicated and detail-oriented Clinical Data Management Project Manager to join our dynamic team in Cambridge. In this pivotal role, you will oversee the management of clinical data projects, ensuring that all data is collected, processed, and reported accurately, in compliance with regulatory standards.The ideal candidate will possess strong organizational skills, an ability to manage multiple projects simultaneously, and a passion for delivering high-quality results. You will collaborate with cross-functional teams to drive project success and enhance data integrity.

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.

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.