Global Clinical Trials Program Manager

Teleflex; Bülach; Vor Ort; CHF 120.000 - 180.000; Vollzeit

Zusammenfassung

Teleflex in Switzerland seeks a professional to lead and oversee clinical trials from planning to completion, coordinating cross-functional teams, managing investigator relationships, and reporting progress to management.

The role requires a university degree in science or medicine, at least two years' experience in global trials, familiarity with ethics and authorities, and English fluency; German is a plus.

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 ethic 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

Clinical trials mgmt

Budget planning

Vendor management

Cross-functional lead

Regulatory liaison

Study documentation

English fluency

Ausbildung

Science/Medical degree

Jobbeschreibung

Teleflex in Switzerland seeks a professional to lead and oversee clinical trials from planning to completion, coordinating cross-functional teams, managing investigator relationships, and reporting progress to management.

The role requires a university degree in science or medicine, at least two years' experience in global trials, familiarity with ethics and authorities, and English fluency; German is a plus.