Global Project Manager - Rare Disease and Oncology Trials

Ergomed; North Carolina; On-site; USD 90,000 - 130,000; Full time

Job summary

Ergomed is seeking a Project Manager to lead international clinical trials within a CRO framework. The role focuses on oncology and rare disease programs, coordinating cross‑functional teams and external providers to meet milestones and budgets.

You will act as a key liaison with sponsors and Ergomed senior management, ensuring rigorous adherence to regulatory and quality standards across global studies. A strong background in trials and stakeholder management is essential.

Qualifications

• Experience as a Project Manager of international clinical trials in a CRO environment.
• Knowledge of Oncology and Rare Disease therapeutic areas.
• Experience in selecting and managing external service providers.
• Strong analytical, organizational and communication skills.

Responsibilities

• Ensure that projects are delivered on time, within budget, and agreed scope, maintaining the appropriate industry, sponsor and Ergomed quality standards.
• Liaise with project team members, provide training where needed and ensure correct allocation to tasks.
• Develop, review and edit project plans to assure consistency with goals and milestones.
• Organization and facilitation of project meetings related to study activities (study organization, initiation, execution, closure).
• Serve as primary point of contact with sponsor and Ergomed Senior Management on project status.
• Represent Ergomed at external meetings, providing liaison with scientific/medical experts and for committee meetings (EC/IRB).
• Develop and edit SOPs to assure regulatory consistency and develop study-related training programs.
• Contribute to bid defense activities.

Skills

Analytical skills

Organizational skills

Communication skills

Education

Bachelor’s degree in science

Job description

Ergomed is seeking a Project Manager to lead international clinical trials within a CRO framework. The role focuses on oncology and rare disease programs, coordinating cross‑functional teams and external providers to meet milestones and budgets.

You will act as a key liaison with sponsors and Ergomed senior management, ensuring rigorous adherence to regulatory and quality standards across global studies. A strong background in trials and stakeholder management is essential.