The Mobile Site Vehicle Specialist supports clinical trials by managing mobile clinical sites, including logistics, supply management, and technical troubleshooting.

The Senior Specialist oversees training compliance and delegation documentation for clinical research studies, ensuring adherence to regulatory standards and improving operational efficiency through cross-functional collaboration.

The Senior Associate, Operational Excellence will manage site operations, ensure regulatory compliance, lead staff development, and support business growth in clinical research.

Oversee study training compliance and DOA matrix management, ensuring regulatory alignment and operational excellence. Lead a high-performing team to optimize processes and prepare for audits.

The Advisor, Talent Acquisition will enhance sourcing strategies and lead recruiting for PRN positions, mainly phlebotomists and RNs, while managing relationships with healthcare professionals and internal stakeholders.

The Specialist coordinates user access and management for clinical systems, monitors compliance, supports onboarding/offboarding, and collaborates with stakeholders to ensure study readiness and system functionality.

As a Specialist in Regulatory Operations, oversee compliance and regulatory activities for clinical trials, particularly for U.S. sites, ensuring adherence to FDA and global standards. Support IRB submissions and maintain essential regulatory documentation.

The Specialist, Regulatory Operations oversees regulatory activities for clinical trials, ensuring compliance and supporting site operations. Responsibilities include managing IRB submissions, regulatory documentation, and collaborating with cross-functional teams.

The Senior HR Business Partner will align business strategy with people plans, oversee talent management, ensure compliance in HR practices, and mentor junior HR staff.

The Senior Software Engineer will develop full-stack applications using TypeScript, collaborate with designers, implement APIs, and ensure code quality in a remote setting.

The Senior Director, Quality will develop and execute Care Access's quality program, ensuring risk-based compliance and embedding quality across clinical and operational domains.

The Senior Data Engineer will design, develop, and maintain data pipelines, optimize data performance, and collaborate with stakeholders to deliver effective data solutions.

As Provider Partnerships Program Manager, you will manage project structures, analyze data, and enhance provider collaboration to support clinical studies.

The Operational Compliance Specialist ensures compliance in clinical trials, manages CAPA processes, and improves operational quality and efficiency across the region.

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

The Lifecycle Marketing Manager will develop and execute strategies to enhance patient engagement and retention through marketing automation, segmentation, and continuous testing.

The Growth Marketing Manager will optimize digital experiences, improve SEO performance, and drive conversions through technical implementation, data analysis, and collaboration across teams.

The Compensation Analyst supports global compensation programs, providing recommendations, conducting market benchmarking, managing incentive plans, and collaborating with HR teams on data analytics.

The Contracts Specialist will manage the lifecycle of contracts including drafting, reviewing, and negotiating agreements, ensuring compliance with policies and standards, and collaborating with stakeholders.