The Lead Data Engineer will design, build, and operationalize scalable data solutions while driving automation and integration across the Azure ecosystem. They will provide technical leadership, mentor junior staff, and ensure data governance compliance across enterprise analytics initiatives.
Lead accounting operations across accounts payable, accounts receivable, procurement, general ledger activities, and reconciliations while ensuring accurate, timely, and well-controlled financial processes. Develop the accounting operations team, improve and scale processes through automation, monitor financial risks and metrics, and provide analysis and reporting to senior leaders and business stakeholders.
The Senior Clinical Research Associate independently performs and oversees clinical site monitoring activities to ensure protocol and regulatory compliance. They serve as the primary liaison between sponsors and investigative sites while mentoring junior staff and supporting site recruitment and setup.
The Senior Clinical Research Associate independently performs and oversees clinical site monitoring, ensuring protocol and regulatory compliance. They serve as the primary liaison between sponsors and investigative sites while mentoring junior staff and managing site recruitment and setup activities.
The Sr. Clinical Research Associate independently coordinates and oversees clinical site monitoring services, ensuring protocol and regulatory compliance. They serve as the primary liaison between sponsors and investigative sites while mentoring junior staff and supporting site recruitment and setup.
The developer will manage the software development lifecycle from design to implementation, focusing on imaging products and cross-functional collaboration. Responsibilities also include providing technical support, performing code reviews, and authoring comprehensive technical documentation.
The TMF Coordinator is responsible for maintaining the quality, completeness, and compliance of Trial Master File documentation in accordance with global regulatory standards. They will perform document QC, resolve filing discrepancies, and collaborate with cross-functional teams to ensure inspection readiness.
The Senior Clinical Research Associate will oversee site monitoring, study management, and ensure the integrity of clinical trials. They will also act as a mentor to peers, assist in hiring and training, and serve as an escalation point for site or patient issues.
The Senior Clinical Research Associate will act as a subject matter expert, providing mentorship and performance feedback to peers while overseeing site monitoring and study integrity. They will also manage monitoring services for complex projects, assist in hiring and training, and serve as the primary escalation point for site or patient issues.
The Senior Clinical Research Associate will act as a subject matter expert, providing mentorship and performance feedback to peers while overseeing site monitoring and study management. They are responsible for ensuring study integrity, managing site relationships, and guiding teams on patient recruitment and protocol compliance.
The Image Service Coordinator assists in the execution of image services activities, ensuring data integrity and reliability according to regulatory standards. They provide ongoing support to stakeholders, clinical sites, and sponsors throughout the project life cycle.
The Clinical Project Manager will plan, execute, and monitor clinical research projects while acting as the primary liaison for sponsors. They are responsible for managing multidisciplinary teams, ensuring regulatory compliance, and overseeing project timelines, budgets, and documentation.
The Senior Clinical Research Associate acts as a subject matter expert, providing mentorship and performance feedback while overseeing site monitoring and study integrity. They manage monitoring services for complex projects, ensure adherence to SOPs, and facilitate effective communication between site staff and sponsors.
The Senior Proposal Specialist assists the business development team in preparing comprehensive proposal responses and budgets for clinical trial opportunities. They work closely with subject matter experts to ensure high-quality, accurate costing and strategic alignment with sponsor expectations.
The medical writer will research, write, and edit regulatory documents such as protocols, investigator brochures, and clinical study reports while coordinating with authors and stakeholders. They will also act as a project manager for writing deliverables, ensuring adherence to industry standards and timelines.
The ERP System Administrator will serve as the primary functional and technical owner of the Acumatica ERP platform, managing configuration, security, and operational health. They will also lead the integration between SAP Concur and Acumatica while supporting the maturation of procurement and project accounting functions.
The Project Coordinator provides administrative and processing support to medical imaging project teams, including document management and meeting coordination. They also act as the primary point of contact for project queries and facilitate billing and payment activities.
The TMF Associate is responsible for managing Trial Master File content throughout the study lifecycle to ensure it remains complete and inspection-ready. They will collaborate with cross-functional teams to maintain file integrity, perform quality control, and provide training to stakeholders.
The statistician will apply biostatistical methods to support clinical trials, including statistical planning, design, analysis, and reporting throughout the project life cycle. They will act as a subject matter expert, providing guidance to project teams and stakeholders while ensuring compliance with regulatory standards.
Execute full-cycle, multi-country payroll processing ensuring accuracy and compliance across various global jurisdictions. Manage stakeholder inquiries, coordinate with Finance and HR, and lead payroll modernization and system optimization initiatives.
Lead the Data Sciences Department in delivering end-to-end clinical data management services while ensuring regulatory compliance and high quality. Manage operational targets, including staff hiring, performance, budgeting, and the optimization of data management technologies.
Lead the end-to-end delivery of clinical data management services while managing staff performance, utilization, and departmental budgets. Oversee the optimization of data management technology and ensure all deliverables meet quality and regulatory standards.
The Clinical Operations Lead provides oversight of project deliverables, CRAs, and investigator sites to ensure compliance with protocols and GCP guidelines. They act as the primary liaison between the monitoring team and the clinical project team while managing site performance and recruitment strategies.
Design and implement scalable end-to-end data pipelines and architectures using the Azure ecosystem to support AI/ML and enterprise analytics. Provide technical leadership by mentoring junior engineers and collaborating with stakeholders to align data engineering with business goals.
Manage and deliver full clinical site monitoring services, including the design and oversight of project monitoring, training, and regulatory filings. Act as a Lead CRA to coordinate between site staff and project teams while ensuring compliance with SOPs and GCP guidelines.
Manage and deliver full clinical site monitoring services, including the design and oversight of project monitoring and regulatory filings. Act as a Lead CRA to mentor peers and serve as the primary liaison between the project team and sponsors.
Responsible for processing and reporting corporate and project-related financial transactions, including accounts payable, receivable, and collections. Liaises with various stakeholders to resolve billing discrepancies and provides support for financial system testing and training.
Apply biostatistical methods to support clinical trials, including statistical planning, analysis, and reporting throughout the project life cycle. Act as a subject matter expert providing guidance to project teams and contributing to the publication of research data.
Provide administrative and processing support to project teams, including document management and meeting coordination. Act as the primary point of contact for project queries and ensure alignment with quality and regulatory standards.
Manage and deliver full clinical site monitoring services, including the design and oversight of project monitoring, site recruitment, and regulatory filings. Act as a Lead CRA to mentor peers and serve as the primary liaison between the project team and sponsors.
Provide comprehensive administrative and clerical support to the Clinical Operations and Project Management department. Manage paper and electronic documentation, coordinate schedules, and assist with divisional supplies and budget expenses.
Oversee financial activities, maintain accurate records, and ensure compliance with accounting standards and industry best practices. Responsibilities include financial reporting, account reconciliation, payroll, taxation, and implementing internal controls.
Oversees clinical operations and project deliverables, providing leadership and oversight to Clinical Research Associates and investigator sites. Acts as the primary liaison between the monitoring team and the clinical project team to ensure protocol and regulatory compliance.
The Sr. TMF Lead provides expert oversight of Trial Master Files for complex programs to ensure quality, compliance, and continuous inspection readiness. This includes aligning sponsor requirements with CRO processes and mentoring TMF staff from study start-up through close-out.
Develop and manage standard reporting libraries and ad hoc analytical solutions to enhance clinical study data reporting. Analyze departmental operational metrics and support the integration of technical data reporting systems.
Develop and manage a standard library of reporting and analytical solutions to enhance clinical study data reporting. Analyze departmental operational and performance metrics to drive process improvement and optimize technical systems.
Lead the day-to-day operational oversight of the Clinical Monitoring unit to ensure high-quality clinical trial execution. Manage staff, contractors, and third-party providers while partnering with sponsors and researchers to maintain regulatory compliance.
The Sr. TMF Lead provides expert oversight of Trial Master Files for complex programs to ensure quality, compliance, and continuous inspection readiness. This includes aligning sponsor requirements with CRO processes and mentoring TMF staff from study start-up through close-out.
Lead and oversee the Clinical Monitoring unit to ensure high-quality execution of global clinical trials. Manage staff, contractors, and third-party providers while partnering with sponsors to maintain regulatory compliance and operational excellence.
The Business Development Director is responsible for achieving annual sales targets and expanding the client base within the Eastern US and Canada region. This includes leading proposal development, managing client relationships, and coordinating with cross-functional teams for bid defenses and contract negotiations.
Provide strategic and operational leadership over the accounting function, ensuring the integrity and accuracy of all financial reporting. Oversee the full accounting cycle, ERP system ownership, tax compliance, and the management of payables and receivables.
Lead the global delivery of full-service clinical trials by providing strategic oversight to project management and finance teams. Drive organizational strategy, process optimization, and operational performance while acting as a trusted partner to sponsors and clients.
Support financial planning and analysis activities, including revenue forecasting, profitability analysis, and budget development across product lines. Act as a liaison between finance and operational groups to track project financial metrics and identify cost-saving opportunities.
The Statistician will apply biostatistical methods to support clinical trials, including statistical planning, design, analysis, and reporting. They will also act as a subject matter expert, providing guidance to project teams and stakeholders while ensuring compliance with regulatory standards.
The Statistician will apply biostatistical methods to support clinical trials, including statistical planning, design, analysis, and reporting. They will act as a subject matter expert, providing guidance to project teams and stakeholders while ensuring compliance with regulatory standards.
The role involves planning, managing, and evaluating the delivery of the Clinical Monitoring unit while ensuring compliance with regulatory requirements. It also includes managing team performance and collaborating with internal and external partners to improve service delivery.
