Suvoda is a global clinical trial technology company shaping digital experiences that enable clinical trial sponsor and site professionals to take full command over the inherent logistical complexity behind mission-critical and time-sensitive patient interactions in life-sustaining studies for therapeutic areas such as oncology, central nervous system, and rare disease.
Supporting clinical trials means supporting unique experiments that are inherently complex, high-stakes, and dynamic. It is imperative that Suvoda staff working with clients, end-users, or the systems that client and end-users interact with understand the clinical trial industry, regulations, Suvoda’s software products and processes, and especially the specificities of the unique trial in question before taking any actions they may alter the data of the system in question.
Responsibilities:
Requirements:
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As set forth in Suvoda’s Equal Employment Opportunity policy, we do not discriminate on the basis of any protected group status under any applicable law.
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Manage multiple software projects in logistics and last-mile delivery, coordinating cross-functional teams, client communication, delivery planning, risk management, and AI-enabled project workflows.
Manage lightweight projects end to end within a Product & Technology PMO, while supporting governance, stakeholder reporting, meetings, and PMO operations as you develop your project management skills.
Support the planning and delivery of clinical research and biometrics projects by coordinating cross-functional teams, tracking timelines, budgets, risks, and quality, and maintaining clear client and team communication.
Coordinate website development projects by tracking milestones, organizing cross-functional teams, translating client requests into actionable tasks, and surfacing blockers to keep delivery on schedule.
Coordinate project plans, timelines, documentation, and stakeholder communication across multiple active projects, keeping deliverables on track and surfacing risks and blockers early.
