Associate Director of Supply Chain Management

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.

Who is BlueRock?BlueRock Therapeutics LP is an innovative clinical-stage biotechnology company specializing in cell therapy. Our mission is to develop groundbreaking medicines for individuals affected by neurological and ophthalmic disorders. Our lead investigational therapies, bemdaneprocel (BRT-DA01) for Parkinson’s disease and OpCT-001 for primary photoreceptor diseases, exemplify our commitment to transforming patient care. Founded in 2016 as a collaboration between Versant Ventures and Leaps by Bayer, our culture is characterized by resilience in the face of challenges, a sense of urgency in advancing medicine, integrity in our mission, and a strong community focus.What Are We Doing?At BlueRock, we leverage cutting-edge science to convert universal pluripotent stem cells into authentic, functional cells for allogeneic therapies targeting a wide range of diseases. Additionally, our engineering capabilities allow these cells to produce therapeutic proteins, enhancing treatment outcomes. Our dedication to cellular and gene therapy is unwavering, and we aim to deliver innovative solutions to millions of patients.We are looking for collaborative individuals who thrive in a vibrant and dynamic work environment, committed to advancing state-of-the-art cellular therapies that will improve patients' lives.The Associate Director of Vendor Management will play a pivotal role in managing and optimizing BlueRock’s essential Development vendor relationships, which are critical for the successful execution of our key clinical initiatives. This position is responsible for ensuring vendor performance, governance, and the overall health of relationships across key outsourced services such as CROs, central labs, imaging, and recruitment vendors.This role sits at the intersection of strategic leadership and operational execution, partnering closely with Clinical Operations, Finance, Procurement, and other functional leaders to ensure that vendors meet their contractual obligations, adapt to evolving program needs, and align with BlueRock’s overarching development strategy. The Associate Director will also be instrumental in establishing scalable, data-driven governance for vendors across Development.

Join Integrated Resources, Inc. as an Administrative Contracts Assistant specializing in Clinical Vendor Management. This pivotal role involves supporting our clinical operations team by managing contract processes, ensuring compliance, and facilitating communication between various stakeholders.

We are seeking a detail-oriented Contracts Assistant specializing in Clinical Vendor Management to join our dynamic team. In this role, you will support the vendor management function by ensuring compliance with contractual obligations, assisting with contract negotiations, and maintaining accurate records for all vendor agreements. Your proficiency in contract management software and your keen eye for detail will be critical in this position.

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 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.

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 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.

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 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.

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 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 Integrated Resources, Inc. as a Senior Associate in Controlled Document Management. In this pivotal role, you will oversee the management of critical documents to ensure compliance and operational excellence. Your expertise will contribute significantly to our projects, delivering high-quality results while maintaining stringent regulatory standards.

Join our team as a Senior Associate in Controlled Document Management, where you will play a crucial role in managing and maintaining documentation processes. You will be responsible for ensuring compliance with regulatory standards while supporting a collaborative team environment. Your attention to detail and organizational skills will be key in streamlining workflows and enhancing operational efficiency.

Join our dynamic team as an Associate Cost Manager at AECOM, a leading global firm providing architecture, engineering, and construction management services. In this role, you will be pivotal in managing project costs and ensuring financial success in a range of construction projects.Your responsibilities will include preparing cost estimates, conducting risk assessments, and collaborating with various stakeholders to deliver projects on time and within budget. If you have a passion for the construction industry and a keen eye for detail, we want to hear from you!

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 Bicycle Therapeutics as a Senior Director of Clinical Data Management, where you will lead innovative data strategies to enhance our clinical trial processes. In this pivotal role, you will oversee the collection, management, and analysis of clinical data, ensuring the highest standards of quality and integrity. Your expertise will guide a dedicated team, driving efficiencies and fostering a culture of continuous improvement.This role is crucial in advancing our mission to develop transformative medicines for patients. Collaborate with cross-functional teams to ensure data strategies align with project goals and regulatory requirements.