• Lead and mentor teams of Java engineers, fostering strong modern engineering practices, code quality, and continuous improvement. • Mentor and encourage professional development in teams. • Work with Architecture and own decisions for Java-based payment systems, ensuring scalability, security, and performance. • Remain hands-on in reviewing designs, frameworks, and proof-of-concepts using modern Java and Spring technologies. • Guide the teams in modernizing existing system with performance, reliability and fault tolerance in mind. • Oversee data modeling, API design, and integration patterns across the platform. • Partner with product managers to translate business requirements into technical solutions. • Ensure CI/CD pipelines, automated testing, and DevOps practices are consistently applied. • Ensure maintenance of documentation, system reports, and architectural artifacts (UML, sequence diagrams, etc.) • Up to 25% travel

Role Description To drive continued success in this exciting clinical research field, we are seeking committed, skilled, and customer-focused individuals to join our winning team as Principal Clinical Data Manager for our Markham, Ontario, Canada on-site location, or remotely from a home-based office anywhere in the USA in accordance with our Work from Home policy. - Act as the primary contact person for communication and discussion of topics related to data management timelines and deliverables; requests for out-of-scope tasks; and first line contact for technical or procedural issues. - Perform hands-on data management tasks including, but not limited to, writing database design specifications, test plans for user acceptance testing (UAT), and data transfer specifications. - Responsible for review or to provide data management oversight and approvals for tasks performed by Data Management support team members to ensure quality deliverables. - Facilitate and participate in UAT, as necessary. - Review data, issue queries, and resolve queries from various data sources (e.g., medical coding, medical history, adverse events, procedures and medicinal products, and external data). - Assist other Clinical Research Organizations, Sponsor, or Investigative Sites with resolving queries. - Perform third party non-Case Report Form data management activities. - Plan, manage, and perform data processing and data management activities for assigned projects to ensure tasks are performed in a timely manner and in compliance with trial Sponsors’ requirements. - Accurately and efficiently validate electronically captured data. - Lead efforts in writing clear queries on missing data and data points failing pre-defined range checks and/or logical checks. - Validate and disseminate real-time study monitoring reports to Sponsor and internal team members. - Review database edit check specifications for assigned studies. - Lead efforts in developing and maintaining standard database validation checks for common modules as well as for therapeutic/drug area specific modules. - Perform training on the electronic data capture (EDC) system, dataflow, and quality control (QC) processes to clinical trial personnel. - Participate in project kick off meetings, investigators meetings, and regular project management team meetings. - Perform study-level resource planning and management, including the review of team members’ timesheet reports. - Manage the process of database modifications (after go-live) due to protocol amendments or study needs. - Develop and maintain the Data Management Plan (DMP). Document deviations from the DMP. - Assist in development and implementation of clinical data standards, training standards, project management, and data management technologies. - Develop and maintain the Data Quality Review Plan (DQRP). Coordinate with programmers to complete the programming and validation of the listings and summary tables as specified in the DQRP. - Assist in the development of project bids, billing, tracking of out-of-scope tasks, and participate in bid defense meetings. - Perform project tracking and maintain project milestones and timelines. Report and resolve any issues with defined timelines and deliverables to the next line of management. - Promote effective project management practices. Review and assess timesheet summary reports for assigned projects. - Follow up on regulatory requirements, industry trends, benchmarks, and best working practices in data management by reading and participating in relevant training and/or association activities. - Participate in and contribute to CDM departmental improvement initiatives. - Define and monitor clinical trial data flow and QC processes in accordance with corporate Standard Operating Procedures, Good Working Practices, and departmental guidelines. - Provide training to study site and Sponsor personnel on data entry and review (electronic data capture studies), data flow, and QC processes. - Cooperate and assist the Quality Assurance (QA) department with QA audits on assigned databases. - Ensure project team maintains and prepares final archival of data management documentation relevant to the assigned clinical trials and assist the corporate archivist in assembling and archiving such documentation. Qualifications - M.Sc. or B.Sc. in a related field. - Ten (10) years of related experience. - Demonstrated an in-depth understanding of clinical trial data management concepts, processes and procedures, relevant issues related to or impacting clinical data management, as well as pharmaceutical clinical trial regulations, industry guidance, conventions and standards. - Demonstrated leadership ability to effectively manage clinical trial data management activities and integrate them with the entire clinical trial operation. - Must communicate effectively, orally and in writing, with personnel on all professional and administrative levels. - Excellent presentation skills and the ability to build relationships with both internal and external clients. - Demonstrated ability to effectively organize and integrate the activities of information processing. - Must be well organized, able to work independently, and manage multiple projects/tasks appropriately. - Demonstrated knowledge of Data Management processes and data flow with the skill to ensure quality delivery. Benefits - Robust benefits package to support your health, well-being, and growth, including medical, dental, and vision coverage. - Life & AD&D insurance. - Short- and long-term disability. - Tuition reimbursement. - Fitness reimbursement. - Employee assistance program (EAP). - Pension plan. - Generous paid time off and sick leave. - Opportunity to earn a performance based bonus. - Estimated Salary Range: $130,000 - $165,000.

• Own the end-to-end success of strategic private equity or holding company accounts—accountable for outcomes across all OpCos, from pre-sale through long-term value realization. • Partner with Account Executives on strategic and PE deals to define scope of work aligned to the BuildOps PS catalog (core implementation, ERP migration, tenant migration, data, training, integrations), set clear implementation expectations, and qualify account readiness for kickoff. • Lead deployment strategy and program planning across the private equity parent and each operating company—defining program phase, governance cadences, risk/issue management, and cross-OpCo dependencies. • Coordinate cross-functional teams including BuildOps Implementation Managers, data/ERP specialists, Customer Success, and Support to deliver against a clear, scoped plan and standard methodology. • Maintain a multi-year account plan spanning adoption and utilization targets by holding company and operating company, identify expansion opportunities (additional modules, integrations, new OpCos), and ongoing PS engagements. • Represent BuildOps in executive settings including steering committees and executive business reviews with PE operating partners, C-suite stakeholders, and OpCo leadership—crafting crisp narratives that connect implementation details to business outcomes. • Champion best practices and reusability across the portfolio—ensuring documentation (runbooks, process maps, RACIs) is captured and reusable across OpCos to scale delivery excellence.

Role Description The role is for an Elementary Case Manager/Compliance Coordinator. - Caseload is approximately 55 IEPs, 12 504s. - Fully remote, 1099 contract opportunity. - Join our pool of educators who have access to our educator portal, where you can select the jobs aligned to your certification as they become available according to our school and district partners. - This is a 1099 Independent Contractor position following the school district's calendar. - Immediate start dates are based on available placement opportunities upon completion of the application process. Qualifications - Valid Connecticut teacher certification in SPED is required. - Must have a Bachelor's Degree from an accredited college/university. - Must be authorized to work in the United States. Requirements - Laptop or desktop computer, webcam, headset, and reliable internet access. - Complete our recruitment process, and submit a background check as part of the application process. - Prior online teaching experience is a plus! Benefits - This is a contract position and does not include benefits.