Global Clinical Trials Lead: Study Management & Vendors

Teleflex; Zürich; Hybrid; CHF 120.000 - 160.000; Vollzeit

Zusammenfassung

Teleflex is seeking a qualified professional to lead and oversee clinical trials from planning through completion. You will coordinate cross-functional teams, manage investigator relationships, and report progress to management.

The role involves budgeting, vendor management, and ensuring adherence to ISO 14155 and ICH-GCP standards, with regular site visits to investigators and interfaces.

Qualifikationen

• University degree or equivalent in scientific or medical field.
• At least two years of experience in designing, planning, executing, analyzing and reporting global clinical trials.
• Experience in clinical research would be an advantage.
• Experienced in dealing with ethics and other competent authorities.
• Fluency in English is a must, and German would be an advantage.

Aufgaben

• Manage the entire lifecycle of clinical trials.
• Define and author clinical investigation documents by ISO 14155, ICH-GCP, and applicable standards.
• Plan and control the budget, supervise the monitoring for assigned clinical studies.
• Lead the study cross-functional team.
• Responsible for Vendor selection and management.
• Report relevant details and milestones to the management.
• Maintain regular visits with study investigators and other study specific interfaces.

Kenntnisse

Fluency in English

German language

Ausbildung

University degree or equivalent in scientific or medical field

Jobbeschreibung

Teleflex is seeking a qualified professional to lead and oversee clinical trials from planning through completion. You will coordinate cross-functional teams, manage investigator relationships, and report progress to management.

The role involves budgeting, vendor management, and ensuring adherence to ISO 14155 and ICH-GCP standards, with regular site visits to investigators and interfaces.