Global Head of R&D, Preclinical to Early Phase Development, excellent
Nr ref.: /JOBS.pl
Seeking an experienced PhD or MD expert in Discovery and Early Phase Clinical Development to join a global team and provide leadership to the global medicine development activities.
As an expert within the field of Discovery and Early Phase Clinical Development, this opportunity offers career advancement you need to showcase your exceptional skills and progress into a Director role.
With strong ideas, and the ability to move these forward into tangible actions, you will be an innovative leader who can influence the late development clinical strategies to ensure the company is not only successful, but market leaders. You will be responsible for delivering plans that deliver medically differentiated therapies that provide meaningful improvement to patients.
As a strategic thinker, you will participate in shaping the progress of Development moving forward. With your expertise within Discovery and Early Phase Clinical Development, you will also take responsibility for the development and successful execution of the Development plan for assigned molecules and indications.
Bringing a wealth of experience from your chosen career path so far, you will inspire and motivate your teams and peers whilst ensuring they have the opportunity to develop and strengthen their own skills and experience.
Within this key strategic role, your actions will help shape the future of Discovery and Early Phase Clinical Development and will have a direct impact on patient's lives.
Your contribution will be important and high profile with a global focus within this truly international team. Provide input to the development of the Preclinical and Clinical Development strategy. Develop the CD plan and ensure effective and efficient execution.
QUALIFICATIONS / EXPERIENCE REQUIRED:
PhD or M.D. required
A recognised expert in the field.
Experience with clinical trials would be an advantage
An understanding of Discovery Early Phase drug development
Experience submitting an NDA/BLA to regulatory authorities in Europe and/or the U.S. would be an advantage
Experience authoring a global preclinical and clinical development plan and publishing results of a clinical drug trial in a referred journal
Academic/teaching background would be preferred
Broad experience in the principles and techniques of data analysis, interpretation and clinical relevance (e.g., ISS, ISE, competitor data, etc.)
Comprehensive understanding of product and safety profiles
In-depth knowledge of medical aspects of GCP (Good Clinical Practice), ICH (International Conference on Harmonisation of Technical Requirements for
Familiar with competitive activity in the field
Want to find out more and APPLY NOW?
To find out more about this and other exciting opportunities based in the UK and Europe then please contact Christopher Swain now for an informal and confidential chat about industry possibilities. Send your C.V. to or call .