9 ICON PLC jobs in England & Wales

As a Clinical Development Scientist you will be joining the world's largest & most comprehensive clinical research organisation, powered by healthcare intelligence. At this role you will lead a clinical sub-team or support the clinical sub-team and the global program team to build global clinical development plans and contribute to the development of asset level and therapeutic area strategies. Responsible for overseeing the clinical development strategy development and execution for one or several projects, contributing to the development of clinical & regulatory strategy, and representing the clinical program at regulatory meetings and before external audiences. This is role is for fixed term 4-6 months contract and is home based What you will be doing:

• Lead or support the clinical sub team and oversee the design and execution of one or two clinical studies.
• Represent Clinical Development on the Global Program Team and in presentations at management and review committees
• Lead a clinical subteam and prepare a clinical development strategy. May lead one or more clinical study teams in the preparation of clinical study related documents including protocols, charters, statistical summary reports, meeting presentations, publications, and clinical sections of regulatory documents
• Determine appropriate advisory board experts and lead the team in preparation for meetings.
• Critically evaluate available information about diseases of interest to the disease area and the competitive landscape and synthesize information succinctly to support dissemination and incorporation into clinical development programs, asset plans and therapeutic area strategy.
• Serve as the Medical input to the Global Development Team / Subteam and the Medical Expert for clinical study team development Team / Subteam and the Medical Expert for clinical study team.
• Support business development activities, such as due diligence and research collaborations
• May serve as the Translational Science lead for one or more programs
  
  MD or equivalent (PharmD with Clinical Development experience); Board Certification preferred
• >5 years of clinical experience preferably within industry
• Experience as a medical monitor for clinical trials required
• Regulatory experience preferred
• Publication in peer reviewed journals
• Advanced knowledge of the assigned therapy area (Endocrinology, bone metabolism or general internal medicine) and the capability to interpret, discuss, and represent trial- or program-level data are desired.
• Experience in medical responsibilities on a cross-functional team preferred