Global Clinical Program Manager

Vor 6 Tagen


Rotkreuz, Zug, Schweiz Hays Vollzeit CHF 120'000 - CHF 180'000 pro Jahr

Our client combines science, data and insights to transform the way diseases can be prevented, diagnosed and monitored. Their medical assays, digital solutions and services help people live healthier lives.

The Ideal Candidate possesses extensive knowledge and experience in
project management, clinical program management within the context of clinical studies, as well as significant experience with Good Clinical Practice (GCP)
.

General Information:


• Start Date: , latest Possible Start Date: , but earlier start date preferred


• Planned Duration of Employment: 1 year


• Workplace: Basel, Rotkreuz


• Workload: 80%


• Home Office: TBC

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

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