Job Description

For this exciting position my client is looking for the following:
Co-ordinate all medical staff all safety data review
Manage clinical trials and all their activities including but not limited to recruitment,protocol writing,site selection and drug release,coordinate work on all multi disciplined projects.
evaluate and make your recommendations for selection of contractors involved with the projects.
Report on the study progress and recruitment within the agreed timelines including reacting to any issues that may arise.
Organise and lead clinical study meetings and advise on budgetary requirements when necessary.
The above is just some of the responsibilities that this role requires.
In addition you will have the following:

PhD/bachelors degree
5+ years as a senior clinical trial manager or senior clinical research associate
Excellent understanding of ICH GCP and relevant regulatory requirements
Excellent communication skills both externally and internally
the ability to lead and motivate within a rapidly changing environment
Ability to evaluate and act on relevant data and be able to write reports on clinical development and propose study plans and ideas.
Work well under pressure
Excellent problem solving skills.

Due to the responsibility of the position there is an excellent salary on offer for the right candidate

Qualifications/Skills Required

clinical,project manager,senior