Overview
In this role, you will lead the CSO’s insourcing model for FSP staff across country and site operations. You will partner with CSO leadership and cross-functional teams to ensure consistent processes, clear roles, and high-quality delivery in clinical trial execution. You’ll shape operational strategy, oversee trainer onboarding, and drive continuous improvement across regions. This position offers impact on trial execution at scale and alignment with global governance, quality, and delivery expectations. A key hook is enabling efficient, site-centric execution within a growing biopharma landscape.
Verantwortungsbereiche
- Manage 20–25 FSP staff across the clinical portfolio to support CSO objectives
- Lead resource forecasting, assignment, and prioritization for regional delivery and annual plan commitments
- Develop and implement role-specific processes, guidance, and quality expectations
- Design and implement training and onboarding programs with FSP vendors and stakeholders
- Oversee onboarding/offboarding of FSP resources ensuring role clarity and policy compliance
- Represent CSO in FSP vendor governance, oversight, and performance forums
- Monitor and report FSP performance metrics, quality indicators, workload trends, and delivery risks
- Partner with CSO leaders, study teams, Medical, Quality, and other stakeholders to align on goals and continuous improvement
Zentrale Anforderungen
- Approximately 12 years of clinical research, clinical operations, country/site operations, or project management experience
- Experience managing resources, vendors, and cross-functional stakeholders; line management advantageous
- Proven ability to oversee FSP staff, including resource planning, training, performance management, and workload prioritization
- Strong cross-functional knowledge of drug development including clinical trial phases I–IV
- Effective line management and mentoring skills
- Excellent leadership, communication, and organizational skills
- In-depth knowledge of GCP, ICH guidelines, regulatory requirements, and quality expectations for global clinical development
- Strong project management capabilities
- Collaborative mindset
- Strong leadership and mentoring
- Effective communication across geographies
- Clinical operations oversight
- Resource planning and forecasting
- Vendor governance and performance management
Associate Director, Country Site & Operations FSP Oversight Manager in Baar Arbeitgeber: Biogen Idec
Biogen ist ein hervorragender Arbeitgeber, der Ihnen die Möglichkeit bietet, in einer dynamischen und innovativen Umgebung zu arbeiten, während Sie die globale Omnichannel-Transformation im Bereich Kundenengagement leiten. Unsere Unternehmenskultur fördert Zusammenarbeit und kontinuierliches Lernen, unterstützt durch umfassende Programme zur Mitarbeiterentwicklung und strategische Initiativen, die darauf abzielen, die Kundenbindung zu verbessern. Darüber hinaus profitieren Sie von einem flexiblen Arbeitsumfeld und der Chance, an vorderster Front der digitalen Transformation in der Biotechnologiebranche zu stehen.
