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The Sr. Technical Project Manager will lead teams in navigating the complexities of drug development, ensure effective collaboration, and deliver impactful outcomes for healthcare clients.

The Accounts Payable Coordinator will process vendor invoices, manage payments, maintain vendor relationships, and improve payment processes, requiring attention to detail and communication skills.

The Safety & PV Specialist I enters ICSR data, maintains safety tracking, and assists in reporting for clinical trials and safety programs.

Conduct on-site and remote monitoring of clinical research studies, ensure compliance with clinical practices, and manage project components efficiently.

The Senior Site Contracts Lead will oversee site contracts, collaborate with teams, and ensure compliance while driving the clinical development process.

The Safety & PV Specialist I processes and manages Individual Case Safety Reports (ICSRs), ensures data accuracy, and maintains proper documentation for clinical trials and post-marketing programs.

The Senior QA Tester will develop and maintain automation solutions, enhance test coverage, and improve quality in agile environments, collaborating with teams to define test strategies and ensure robust documentation processes.

The role is responsible for managing site activation processes, ensuring compliance with project requirements, monitoring finances, and facilitating local regulatory submissions under supervision.

The role requires a Senior Statistical Programmer with expertise in R and R Shiny to create visualizations and work with clinical trial data, alongside managing multiple studies and effective communication.

Seeking a QA Tester to design, develop, and maintain automated test solutions using Playwright and TypeScript, improve release quality and testing processes, and collaborate in an agile environment.