Description
Hays ist ein weltweit führender Personaldienstleister, der sich auf die Rekrutierung von Spezialisten konzentriert - sowohl für den Projekteinsatz als auch für Festanstellungen und auf Zeit. In Deutschland, Österreich und der Schweiz vertrauen mehr als 600 internationale Topunternehmen auf unsere qualitätsgesicherten Prozesse, wenn Sie Experten suchen.We are looking for a
Global Study Manager (m/f)
Referenz: -en
Beginn: asap
Dauer: 12 MM
Ort: Region Basel
Branche: Herstellung von pharmazeutischen Spezialitäten und sonstigen pharmazeutischen Erzeugnissen
Ihre Aufgaben:
- Develops operational plans including site monitoring strategies, risk mitigation strategies, trial budgets, site selection, and clinical supplies management
- Builds effective and efficient high performing operations teams and ensures team members are aware of their accountabilities, responsibilities and deliverables
- Creates team culture and promotes team spirit
- Develops and maintains effective working relationships with SMT members, with particular focus on affiliate teams, external CRO (for outsourced teams) and co-development partner study teams
- In collaboration with functional management, coaches, mentors, supports, and provides study specific direction to Study Management team members
- Oversees the development and maintenance of study specific manuals created by the GSA
- Ensures operational tracking tools are identified, including systems to meet the needs of the operations team and ensures reporting to the GSL
- Develops and manages clinical study budgets (including HQ budget) and contributes to staffing/resourcing plans
- Communicates variances in the budget and action plan for resolution to the GSL
- Establishes study milestones and ensures accurate tracking and reporting of study metrics
- Provides operational input into the development of protocol feasibility questionnaires
Ihre Qualifikation
- Proven clinical development experience of the operational aspects of all stages of clinical studies preferably working in a Global environment and/or including monitoring or leading affiliate teams, working with vendors and/or CROs, drug supply management and planning operational activities to achieve database lock
- Experience of project managing operational aspects of a clinical study including development of timelines, budgets and resource plans
- Good knowledge of ICH GCP
- Proven ability to successfully achieve results within a multi-cultural and geographically diverse team
- Experience of working as part of a large team and leading small study or functional teams, with a proven ability to be an active member of the team and motivate and lead a small team to deliver against commitments
- Well developed written and verbal communication skills demonstrated by an ability to present clear instruction/direction to teams at the same level in the organization and influence at higher levels in the organization
- Project Management
- Collaboration and Teamwork
- Negotiating
- Communication
- Personal Organization
Skills:
- Clinical Project Management
- .NET Development