Jobs at Care Access

Provide medical oversight for clinical trials, ensure participant safety and protocol compliance, perform assessments and study procedures, review safety reports and CRFs, train and support sub-investigators and staff, participate in monitoring/audits, and comply with ICH GCP and regulatory requirements.

The Senior Enterprise Performance Analyst will develop dashboards, analyze performance data, support decision-making, mentor junior analysts, and improve organizational performance.

The Enterprise Performance Analytics Engineer builds and maintains data pipelines and models, ensuring data quality and efficient reporting for analytics teams.

The Principal Investigator will oversee clinical trials, ensuring compliance with study protocols and safeguarding participant safety while providing medical support to study staff and conducting assessments as necessary.

Lead and oversee accounting operations including general ledger, month-end close, balance sheet reconciliations, intercompany and multi-entity consolidation, and international accounting. Provide technical accounting support, maintain internal controls, coordinate audits and tax filings, and drive process improvements. Coach and manage accounting team members and partner cross-functionally to ensure accurate, timely financial reporting and compliance.

Support decentralized field operations and clinical events by transporting and managing supplies and inventory, organizing vehicle interiors, troubleshooting basic vehicle issues, generating asset and inventory reports, and using Excel and web-based inventory tools. Work requires long-distance driving, extended travel including weekends/holidays, and collaboration with fleet, HR, and clinical teams.

Support day-to-day AP/AR, billing, cash application, reconciliations, and transaction processing. Prepare and review vendor bills and customer invoices, assist month-end close, research discrepancies, respond to stakeholders, and support process improvements and reporting to ensure accurate financial records and audit readiness.

Provide medical oversight for clinical trials, ensuring participant safety and regulatory compliance. Perform examinations and study procedures, review safety reports and case report forms, train and support sub-investigators and staff, and participate in monitoring, audits, and sponsor meetings following ICH GCP and protocol requirements.

The Principal Investigator oversees clinical trials, ensuring compliance with study protocols, protecting participant safety, conducting assessments, and training staff. Responsibilities include reviewing protocols and safety reports, maintaining case forms, and participating in monitoring visits.

Provide medical oversight for clinical trials, ensuring participant safety and GCP compliance. Perform physical assessments and study procedures, review safety reports and case report forms, train and support study staff, participate in monitoring and sponsor meetings, and ensure regulatory readiness and auditing access.

Lead daily operations of the Warsaw clinical research site to meet enrollment, retention, data quality, and sponsor commitments. Ensure regulatory and ICH-GCP compliance, manage study start-up and monitoring readiness, lead and develop CRC and PSC staff, foster investigator and sponsor relationships, drive site performance and operational improvements, and support financial and resource planning.

The CTMS Operations Analyst ensures quality and technical support for CTMS operations, handles build configurations, reporting, and user training, while improving processes throughout the study lifecycle.

Lead end-to-end video production from concept and scriptwriting through pre-production, on-set directing, and post-production. Manage workflows, cross-functional stakeholders, vendors, and revision cycles. Produce event coverage, patient stories, and brand features, often on-location. Maintain high creative quality, organization, and adaptability in a fast-paced environment while delivering portfolio-quality narrative video for healthcare-focused storytelling.

Support QA for traditional and decentralized clinical trials by conducting site quality reviews, regulatory binder reviews, audits, CAPA management, SOP development, QMS administration, inspection readiness, training delivery, and cross-functional compliance advising. Provide operational audit support, track QA metrics, assist RFP/RFI responses, engage with digital technologies and AI project quality, and help maintain data integrity and regulatory compliance per GCP and FDA/ICH guidance.

Build and maintain Playwright-based end-to-end test automation across UI, API, and integration layers. Author release validation documentation for GxP and 21 CFR Part 11 compliance. Integrate quality gates in CI/CD, partner with engineers to shift testing left, and explore AI/LLM-assisted test generation and failure triage to scale coverage and reduce manual effort.

Lead and optimize global financial transactional operations (AP, AR, Revenue), drive ERP and automation initiatives, improve cash flow and controls, manage reporting and month-end, and build a high-performing financial operations team while partnering cross-functionally to align processes and support audits and forecasting.

The Sub-Investigator oversees clinical research studies, administers investigational products, conducts physical exams, and ensures compliance with protocols. Responsibilities include patient assessments, data collection, and collaborative management of clinical trials, involving travel and telemedicine.

Designs and maintains enterprise dashboards and reports, performs SQL-based analyses, identifies operational performance drivers, partners with cross-functional leaders, provides ad-hoc analytics, and mentors junior analysts to improve organizational outcomes.

Lead operations and performance for multiple clinical research sites across a region, ensuring GCP/FDA/ICH compliance, timely enrollment, data quality, budget oversight, staff leadership and development, stakeholder management, audits, and risk mitigation. May perform Clinical Research Coordinator duties at sites as needed.

Support day-to-day AP/AR, billing, cash application, reconciliations, and reporting. Prepare and review invoices and vendor bills, research variances, resolve routine discrepancies, assist month-end close, and collaborate with cross-functional teams to maintain accurate financial records and controls.