Medical Director, Clinical Development

Medical Director, Clinical Development
GMC Registration is essential
London, UK
Attractive salary, bonus and package (DOE)
 

Albion Rye Associates are proud to be assigned as the exclusive recruitment partner to a rapidly expanding, international, high science biotech specialising in developing treatments for rare genetic disorders.

My client, based in Central London are looking for an established Medical professional with a minimum of 3 years Clinical Development experience, ideally within rare disease, oncology or immunology to lead development across multiple on-going studies across the portfolio.

.Responsible for:

• Clinical development plans
• Manage the clinical studies
• Lead regulatory documentations/presentations
• Writing and executing regulatory communications alongside the Clinical team

Experience required:

• Gene therapy/immunology/haematology-oncology background
• At least 3 years experience within Biotech or Pharma (within a Clinical Development team)
• Understanding of regulatory environment, GCP/ICH and GMP
• Experience dealing with external regulatory agencies

This role has been assigned exclusively to Albion Rye Associates, all applications must to Jake Byrne, Managing Director for consideration.