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Medable is seeking an experienced eCOA Project Manager to lead the deployment lifecycle of its clinical trial platform. You will manage end-to-end software implementation projects from kick-off through go-live, ensuring alignment with trial-specific requirements and regulatory compliance.
Key responsibilities include: managing project scope, timelines, and budgets; collaborating with solution design teams to translate clinical trial protocols into system specifications; developing adaptive project plans that accommodate evolving client needs; implementing robust change management practices; educating clients and internal teams on software capabilities; and serving as the primary point of contact for clients throughout the project lifecycle.
You will work across cross-functional teams including developers, product managers, and clinical trial experts to deliver solutions meeting complex regulatory expectations. The role requires proactive risk identification and mitigation, comprehensive project documentation, knowledge transfer facilitation, and continuous process improvement through data-driven analysis.
Required qualifications: minimum 6 years of project management experience, proven track record managing full-lifecycle software implementations, advanced change management expertise, and comprehensive understanding of clinical trial domains including eCOA, ePRO, EDC, and DCT. Strong knowledge of clinical trial data management and regulatory compliance frameworks is essential.
Desired qualifications include a Bachelor's degree in Computer Science or Health Informatics (Master's preferred) and project management certifications such as PMP or PRINCE2. The role requires technical aptitude, exceptional interpersonal and communication skills, and ability to manage multiple complex priorities simultaneously. Flexible travel schedule required for domestic and international client engagement.
