Clinical Trial Manager: CRO & Site Operations Lead

CDR-Life AG; Thalwil; In loco; CHF 90.000 - 130.000; Tempo pieno

Descrizione del lavoro

CDR-Life AG in Switzerland is seeking a Clinical Trial Manager responsible for planning and managing trials in outsourced settings. You will act as a key operational contact for CROs, sites, and vendors, ensuring delivery within quality, timelines, and budget while adhering to ICH-GCP and company procedures.

The role requires a hands-on professional with ownership, strong collaboration, and travel readiness to support global multi-center trials and sponsor monitoring activities; you will develop

Competenze

• Master's degree or higher in life sciences, healthcare or related field.
• 2+ years of trial management experience in biotech, pharma or CRO.
• Experience with CRO/vendor oversight and site monitoring (CRA).
• Global multi-center trial operations knowledge and travel ability.

Mansioni

• Plan and execute clinical trials from startup to close-out.
• Coordinate with CROs, sites and external vendors.
• Oversee budgets, timelines, quality, and deliverables.
• Support feasibility, contracting, and performance assessments.
• Ensure regulatory compliance with ICH-GCP and local regulations.

Conoscenze

Clinical trial management

CRO/vendor oversight

Oncology monitoring

Regulatory knowledge

Formazione

Master's degree in life sciences

Strumenti

EDC systems

eTMF systems

Descrizione del lavoro

CDR-Life AG in Switzerland is seeking a Clinical Trial Manager responsible for planning and managing trials in outsourced settings. You will act as a key operational contact for CROs, sites, and vendors, ensuring delivery within quality, timelines, and budget while adhering to ICH-GCP and company procedures.

The role requires a hands-on professional with ownership, strong collaboration, and travel readiness to support global multi-center trials and sponsor monitoring activities; you will develop