Ergomed, a specialist contract research organization focused on rare diseases and oncology, is seeking a Senior Project Manager to lead international clinical trials from Raleigh, North Carolina. The role requires delivering projects on time, within budget, and within agreed scope while maintaining industry, sponsor, and Ergomed quality standards. Responsibilities include liaising with project team members, providing training as needed, and ensuring correct allocation of tasks; developing, reviewing, and editing project plans to align with goals and milestones; organizing and facilitating project meetings related to study activities (initiation, execution, closure); serving as the primary point of contact with sponsors and Ergomed senior management for project status; representing Ergomed at external meetings and coordinating with scientific/medical experts across CROs and sponsor companies for committee meetings (e.g., EC/IRB); updating SOPs to ensure regulatory alignment and developing study-related training programs; and contributing to bid defense activities. Qualifications include experience as a Project Manager of international clinical trials in a CRO environment; knowledge of oncology and rare disease therapeutic areas; experience selecting and managing external service providers; strong analytical, organizational, and communication skills; and a Bachelor’s degree in a science-related discipline. When you join Ergomed, you contribute to bringing safe and effective pharmaceutical treatments to patients worldwide and will work with a collaborative, international team

Ergomed, a specialist contract research organization focused on rare diseases and oncology, is seeking a Senior Project Manager to lead international clinical trials from Raleigh, North Carolina. The role requires delivering projects on time, within budget, and within agreed scope while maintaining industry, sponsor, and Ergomed quality standards. Responsibilities include liaising with project team members, providing training as needed, and ensuring correct allocation of tasks; developing, reviewing, and editing project plans to align with goals and milestones; organizing and facilitating project meetings related to study activities (initiation, execution, closure); serving as the primary point of contact with sponsors and Ergomed senior management for project status; representing Ergomed at external meetings and coordinating with scientific/medical experts across CROs and sponsor companies for committee meetings (e.g., EC/IRB); updating SOPs to ensure regulatory alignment and developing study-related training programs; and contributing to bid defense activities. Qualifications include experience as a Project Manager of international clinical trials in a CRO environment; knowledge of oncology and rare disease therapeutic areas; experience selecting and managing external service providers; strong analytical, organizational, and communication skills; and a Bachelor’s degree in a science-related discipline. When you join Ergomed, you contribute to bringing safe and effective pharmaceutical treatments to patients worldwide and will work with a collaborative, international team