Global Clinical Program Manager 80
vor 1 Woche
Background:
With the combined strength in pharma and diagnostics, the aim to improve health outcomes and reduce costs for patients and healthcare systems.
With the diagnostics solutions, medicines and digital products, it will address patient needs along their entire journey - innovating from prevention and screening, to diagnosis, treatment and monitoring, meeting patients where they are and creating more comprehensive offerings.
Excellence in innovation, operations and an unwavering commitment to the people and sustainability underpin all of this.
They combine science, data and insights to transform the way diseases can be prevented, diagnosed and monitored. The medical assays, digital solutions and services help people live healthier lives.
Tasks & Responsibilities :
- The Global Clinical Program Manager is a planning expert in Clinical Operations Program Leadership and is responsible for partnering with key stakeholders and CDMA (Clinical Development & Medical Affairs) functions to manage CDMA related project information to support decision making by: CDMA Project Teams, CDMA Leadership (Chapter & Sub-Chapter), respective Customer Area's (CAs) and Project Teams (PTMs)
- The Global Clinical Program Manager applies project management skills and clinical operations experience to ensure on-time delivery of CDMA related deliverables, within budget and with high customer satisfaction through collaboration with other CDMA Clinical Program Managers (cPMs), global Portfolio & Project Management Office's (PPM) Project Managers (PMs) and/or PPM Leadership
- Drive patient and customer-centricity (mindset, behaviors and actions) by always putting the needs of patients and the customers first
- Partner across diverse regions, cultures, and time zones to create an environment of belonging, inclusion and diversity
- Working across Clinical Development and Medical Affairs communities to identify mutual value and opportunities for collaboration
- Expert of Project Management activities (Budget Planning/Tracking and Reporting, Risk & Change Management, etc.) within Clinical Operations or Diagnostic Product Development Processes
- Guides others in resolving highly complex issues and problems with implications on cross-functional organizational processes and outcomes, ideas and influences senior level stakeholders to adopt a new approach
Must Haves:
- Bachelor degree or Master degree or equivalent relevant experience in a related field
- Minimum of 3 years experience in clinical program management in clinical studies
- Proven GCP experience
- English fluent, German is an advantage
What you will be offered:
- An opportunity to work in one of the world's most important pharmaceutical companies
- Modern campus with plenty of green spaces and meeting areas
- Central location in Basel
- Varied job profile
- Further training opportunities through temptraining
- Working in a dynamic and motivated team
If you are interested please send your application documents addressed to Ms Diana Afonso.
Basel-Stadt Solothurn Aargau Pharma Global Clinical CDMA Leadership Risk Change Management
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