Global Clinical Project Lead

Cti; Viseu; Híbrido; EUR 70 000 - 100 000; Tempo integral

Vantagens oferecidas por esta oferta de emprego

Hybrid work opportunities

Resumo da oferta

CTI is seeking a Clinical Project Manager with strong leadership to oversee global clinical trials from start-up to analysis. The role requires coordinating functional areas to ensure ICH and GCP compliance, overseeing budgets, timelines, and deliverables, and guiding cross-functional teams through multiple simultaneous projects.

The ideal candidate will have a minimum of 6 years in clinical research, fluency in English, and a background in allied health fields.

Qualificações

• Bachelor's degree in allied health fields such as nursing, pharmacy or health science, preferably with clinical trial management experience or an equivalent combination of education and relevant work experience.
• At least 6 years of clinical research experience (CRO CRA or Research Manager, Site Research Manager, Central Clinical Research Laboratory Manager) or transferable skills in project management in a clinical setting or relatable industry.
• Fluent in English

Responsabilidades

• Plan, implement, evaluate, and complete full execution of assigned clinical trials.
• Provide oversight and coordination of the operational aspects of the functional areas on assigned projects to ensure compliance with ICH, GCP and trial procedures.
• Manage full-scope clinical trial projects including global trials from start-up through analysis phase.
• Coordinate and oversee team members on clinical trials projects and manage multiple projects simultaneously.
• Prepare or provide oversight to the development of trial plans, timelines, budgets, and deliverables.
• Lead client and team meetings to enable effective info sharing, discussion, and decision making.

Conhecimentos

Fluent English

Formação académica

Bachelor's degree in allied health fields

Descrição da oferta de emprego

CTI is seeking a Clinical Project Manager with strong leadership to oversee global clinical trials from start-up to analysis. The role requires coordinating functional areas to ensure ICH and GCP compliance, overseeing budgets, timelines, and deliverables, and guiding cross-functional teams through multiple simultaneous projects.

The ideal candidate will have a minimum of 6 years in clinical research, fluency in English, and a background in allied health fields.