Senior Director, FSP Oversight & CSO Operations

Biogen; Baar; Vor Ort; CHF 220.000 - 320.000; Vollzeit

Zusammenfassung

Biogen Baar, Switzerland is seeking an Associate Director, Country & Site Operations FSP Oversight Manager to lead the FSP insourcing model. You will drive delivery excellence across country- and site-level operations, align stakeholders, and shape CSO strategy while embedding robust processes and quality standards.

With ~12 years in clinical research or operations, you will mentor staff, manage resources and vendors, and ensure regulatory compliance (GCP/ICH).

Qualifikationen

• BA or BSc in a scientific discipline; advanced degree preferred.
• ~12 years of clinical research/clinical operations experience.
• Experience managing resources, vendors, and cross-functional stakeholders.
• Proven ability to manage and oversee FSP staff, including planning and performance.
• Strong knowledge of drug development and regulatory guidelines (GCP/ICH).

Aufgaben

• Lead and manage 20–25 FSP staff across country/site portfolio.
• Forecast resources, assign, and prioritize to meet regional needs.
• Develop and implement role-specific processes and quality expectations.
• Design training and onboarding programs with vendors and CSO leaders.
• Oversee onboarding/offboarding of FSP resources and policy compliance.
• Represent CSO in FSP governance, oversight, and performance forums.
• Monitor FSP performance metrics, quality indicators, and risks.
• Collaborate with regional leaders and study teams to align goals.

Kenntnisse

GCP/ICH knowledge

Regulatory compliance

Vendor governance

Cross-functional leadership

Project management

FSP oversight

Ausbildung

BA/BSc in scientific discipline

Advanced degree preferred

Jobbeschreibung

Biogen Baar, Switzerland is seeking an Associate Director, Country & Site Operations FSP Oversight Manager to lead the FSP insourcing model. You will drive delivery excellence across country- and site-level operations, align stakeholders, and shape CSO strategy while embedding robust processes and quality standards.

With ~12 years in clinical research or operations, you will mentor staff, manage resources and vendors, and ensure regulatory compliance (GCP/ICH).