Alimentiv

You'll apply **biostatistical methods** to support **clinical trials** from planning to reporting. You'll lead a team of statisticians and SAS programmers, ensuring regulatory compliance and publishing results.

You'll provide unbiased medical guidance to clinical sites and study operations teams, ensuring medical congruency and safety oversight. You'll review critical study materials and data listings to support clinical safety and data management. This role offers the chance to work remotely and collaborate with cross-functional teams in a **CRO environment**.

You'll provide unbiased medical guidance to clinical sites and study teams. You'll support clinical safety, project management, and data management **ensuring medical congruency** at subject and study level. **Review critical study materials** and data listings through the study duration.

You'll serve as the primary **Acumatica ERP** and **Salesforce CRM** administrator, owning day-to-day system operations and driving continuous improvement initiatives. Your core impact lies in optimizing Finance workflows and owning the integration layer between **SAP Concur** and Acumatica via Celigo middleware. This role stands out for its dual focus on business analysis and hands-on system configuration across both ERP and CRM platforms.

You'll lead **clinical monitoring operations** and manage teams delivering **high-quality site services**. Your impact spans resource planning, compliance oversight, and sponsor collaboration. This role offers remote flexibility across multiple US locations.

You'll provide **expert TMF oversight** for complex clinical studies, ensuring quality and inspection readiness. You'll align sponsor requirements with CRO processes and lead **risk-based TMF management** from startup to close-out. This role offers the opportunity to mentor staff and contribute to process improvements at a global CRO focused on GI therapies.

You'll lead **European CRA teams** delivering clinical monitoring for GI-focused trials at a global CRO. Your role shapes **operational policies and resource planning** to ensure regulatory compliance and quality. This position blends leadership and strategic impact in a profit-with-purpose company.

You'll conduct **needs assessments** to identify AI opportunities and **develop roadmaps** aligned with organizational priorities. You'll design and deliver **structured training programs** to build AI proficiency across teams, and prototype solutions using **no-code platforms** like Microsoft Copilot Studio and Power Automate.

You'll support the Data Sciences department in **building advanced analytical solutions** for clinical study data. You'll deploy standard and ad hoc reporting solutions to enhance **operational quality and efficiency**.

You'll support the Data Sciences department in **developing analytical solutions** for clinical study data reporting and analytics. You'll lead reporting standards management and deploy **study-specific reporting solutions**. Your work will enable operational quality through performance metrics analysis.

You'll drive growth for a **CAP- and CLIA-accredited specialty histopathology lab** by identifying new opportunities and building strong sponsor relationships. You'll lead sales strategies from proposal development through contract negotiations, directly impacting the company's market expansion. This role offers **East Coast coverage** with the flexibility of remote work.

You'll lead a **Product Support team** for a **clinical imaging ecosystem**, acting as a player/coach to drive issue resolution and process improvement. You'll coordinate cross-functional support to ensure a **unified customer experience**.

You'll join the BD team supporting the EU/APAC region, driving sales growth by identifying strategic opportunities and managing proposals. Core impact: collaborating with operations to develop cost estimates and lead contract negotiations. Standout: participation in **mentorship programs** and **leadership development initiatives**.

You'll provide **strategic TMF oversight** for complex clinical studies, ensuring **inspection readiness** and **regulatory compliance**. Your work directly impacts **GI therapy advancement** at a global CRO dedicated to gastrointestinal research.

You'll **oversee clinical operations** for a global project, managing a team of CRAs and ensuring compliance with GCP and regulations. Your core impact is **proactive site and country performance management**. This home-based role offers the chance to **lead study tools development** and enrollment strategies.

You'll **manage clinical site monitoring** for complex, multinational projects as a **Lead CRA**, acting as liaison between CRAs and sponsors. You'll **oversee site recruitment and data integrity** while ensuring GCP compliance.

You'll apply biostatistical methods to support clinical trials, handling statistical planning, analysis, and reporting. You'll act as a subject matter expert, providing **statistical support** to project teams and external stakeholders while contributing to **data publication and reporting**.

You'll apply **biostatistical methods** to support **clinical trials and data management**, including statistical planning, design, analysis, and reporting. You'll act as a subject matter expert, providing statistical support to project teams and stakeholders.

You'll drive software projects in the **Medical Imaging** product line using **Agile methodologies**. Your core impact is leading cross-functional teams to deliver high-quality solutions aligned with product strategy and business goals.

You'll lead the clinical monitoring unit for a **global CRO**, ensuring **regulatory compliance** and **high-quality site management**. This remote role spans team management, process improvement, and sponsor relations across multiple countries.

You'll join Alimentiv's Statistical Center of Excellence, applying **innovative biostatistical methods** to support **clinical study design** and implementation. You'll advise clients, oversee **statistical analysis plans**, and contribute to thought leadership.

You'll act as a subject matter expert and lead clinical site monitoring for complex, multinational studies. You'll ensure **GCP compliance** and **site data integrity** while mentoring CRAs and liaising with sponsors. This home-based role offers **direct impact on global clinical trials**.

You'll oversee **clinical operations** for projects at a regional/global level, acting as the primary liaison between CRAs and the clinical project team. You'll ensure **site compliance** with protocols, GCP, and regulations while driving enrollment strategies. This home-based role offers the chance to **impact clinical trials** across multiple regions.

You'll support clinical site monitoring services and provide site management activities for full-service studies. You'll ensure compliance with protocols, SOPs, and regulatory standards. This role offers the opportunity to work **remotely** while collaborating with **international project teams**.

You'll oversee regional CRAs and ensure compliance with study protocols and regulations. You'll serve as the primary operational liaison between CRAs, project teams, and sponsors, **driving site performance** and **quality monitoring activities**.

You'll manage and deliver full clinical site monitoring services for complex, multinational projects. In this home-based role, you'll design and oversee project monitoring, act as a subject matter expert, and maintain collaborative relationships with stakeholders. You'll serve as the **primary liaison** between CRAs and the project team, ensuring **GCP compliance** throughout the study lifecycle.

You'll manage the planning and execution of **clinical research projects**, ensuring compliance with **regulations and corporate policies**. You'll coordinate cross-functional teams and act as the primary liaison with clients and sponsors.

You'll lead a team of developers and testers in delivering **clinical imaging software** within a **regulated healthcare environment**. You'll balance hands-on technical contributions with people management to ensure reliable, high-quality releases. This role offers a unique opportunity to shape both legacy and modern platforms while driving continuous improvement.

You'll support **site management** through remote and onsite visits for clinical trials. You'll ensure **data quality and regulatory compliance** across study systems. This role offers **career growth** across multiple seniority levels.

You'll provide statistical consulting to clients on clinical study design and analysis. You'll apply **innovative biostatistical methods** to support **clinical trial development**. This role offers remote work in Canada or USA.

You'll oversee regional CRAs and investigator sites, ensuring compliance with protocols, GCP, and local regulations. You'll act as the primary liaison between CRAs and the clinical project team, driving enrollment and recruitment strategies. This home-based role offers **project oversight** and **collaboration with global teams**.

You'll act as primary liaison throughout the project life cycle, managing client expectations and leading interdisciplinary teams. Your core impact will be ensuring project milestones, budgets, and quality standards are met for global clinical trials. This role offers the chance to mentor team members and drive operational excellence in a remote environment.

You'll oversee regional CRAs to ensure site compliance with study protocols and regulations. Your core impact is managing site, country, and regional performance, including startup, recruitment, and data quality. This talent pool role offers flexibility for future opportunities.

You'll oversee regional clinical operations, managing CRAs and investigator sites to ensure compliance with GCP and regulations. You'll act as the primary liaison between CRAs and the clinical project team, driving **site performance** and **enrollment strategies**. This role offers the chance to work on **global clinical trials** from a remote home-based setup.

You'll oversee project clinical operations and CRA teams in a remote role. Your impact includes ensuring site compliance with GCP/ICH guidelines and driving recruitment and study deliverables.

You'll lead a **software development and testing team** within a **clinical imaging ecosystem**, acting as a player-coach. Your core impact will be ensuring reliable delivery across legacy and modern platforms. You'll collaborate closely with product and project management to meet **business and clinical needs**.

You'll manage and deliver full clinical site monitoring services for complex, multinational projects. As a lead CRA, you'll act as the primary liaison between CRAs and the project team, **overseeing site recruitment and regulatory filings**. This **remote-based role** offers the chance to work with a global team on innovative clinical trials.

You'll join a talent pool for **Clinical Research Associate** roles supporting **site management and monitoring** across Canada. You'll drive data quality and regulatory compliance through remote and onsite visits.

You'll join a talent pool for CRA roles supporting clinical monitoring in Europe. You'll contribute to site management, data integrity, and regulatory compliance for clinical trials. This proactive opportunity keeps you on file for future openings.

You'll support AI adoption across departments by providing training, guidance, and implementation resources. You'll prototype solutions using **no-code AI platforms** and act as a liaison between tech teams and end users. This role contributes to **AI governance** and organizational capability-building at a health research organization.

You'll support clinical site monitoring services and develop CRA skills in a training-focused role. Your work will drive investigative site compliance and patient recruitment. You'll gain exposure to **remote data review** and **site management activities**.

You'll oversee **clinical operations** for a global project, managing a team of CRAs and investigator sites. Your work ensures **compliance with GCP and local regulations** while driving enrollment and performance metrics. This role offers **full remote flexibility** within a permanent position.

You'll manage clinical site monitoring services for complex multinational projects. You'll act as Lead CRA, liaising between **CRAs and project teams** and ensuring compliance with **GCP and regulatory guidelines**. This remote role offers the chance to mentor peers and shape monitoring strategies.

You'll design and optimize IHC, multiplex IF, and ISH assays, and develop **AI-assisted image analysis pipelines** for a **CAP/CLIA-accredited histopathology lab**. You'll serve as scientific lead for sponsor studies, translating complex data into actionable insights for pharmaceutical clients.

You'll lead **Veeva Vault administration** for Clinical applications (eTMF, CTMS, Study Training, Startup, Site Connect), translating strategic priorities into system solutions. Your core impact is configuring and maintaining the platform to ensure compliance, data integrity, and user adoption. This contract role offers the chance to manage a team while working remotely.

You'll manage Trial Master File (TMF) content throughout the study lifecycle, ensuring **inspection readiness** and **document completeness**. You'll collaborate with study teams on periodic reviews and audits, while maintaining the electronic file repository. This role offers a **remote work arrangement** supporting global clinical operations.