Senior Clinical Project Manager

138386
  • 180000 EUR - 180000 EUR
  • Lachen, Switzerland
  • Permanent
The Role:

This is an exciting opportunity for a leading global pharmaceutical powerhouse headquartered in the picturesque landscapes of Switzerland. We are actively seeking a dynamic and experienced professional to join the team as a Senior Clinical Project Manager (CPM). In this pivotal role, you will play a key part in steering the clinical development initiatives of our innovative pharmaceutical products, contributing to the advancement of healthcare on a global scale. If you thrive in a fast-paced, collaborative environment and possess a wealth of expertise in clinical project management within the pharmaceutical industry, we invite you to explore this unique opportunity to make a meaningful impact in our esteemed organization.
What will you be doing as Senior Clinical Project Manager?
  • Planning, implementation and evaluation of global clinical Phase 1-4 GCP studies   
  • Directing activities of team members to ensure compliance with protocols and overall clinical objectives. Providing input to overall clinical development programs with coagulation and critical care products and lead the development of study protocols
  • Evaluate, analyse and interpret clinical data. Preparing study reports, CTDs, summary reports, expert statements, etc. for Competent Authorities 
  • Keeping track of study budgets, involvement in vendor oversight
  • Interacting with Independent Data Monitoring and Steering Committees (install, update, present results, etc.)
  • Contribute to publications and prepare abstracts, posters and/or presentations for national and international congresses
  • Review scientific literature, participate in continuing education activities or attend conferences and seminars to maintain / keep up to date current knowledge of all aspects regarding clinical studies 
Who are you?
  • PhD or MD background
  • Minimum of 5 / 10 years experience in clinical research (as CPM / 10 years for Senior CPM) in a pharmaceutical or biotechnology company
  • Excellent communication skills to be able to effectively convey messages across to both study team members and other external persons like vendors and external consultants
  • Good organizational, and leadership skills
  • Experience in writing clinical study procedures and other clinical documents
  • Strong project management skills and planning competencies to set plans and execute on time and within budget
  • Experience managing CROs and outside vendors to plan and execute Phase 1- 4 clinical trials
  • Fluent in German and English (written and spoken)
  • Willing to travel up to 30%
If you are interested in this role, please do reach out to laurie@peoplewithchemistry.com or call on 02034332235.



 
Laurie Watts Lead Client Partner

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