Role: Senior Clinical Research Associate
Salary: Up to £50,000 per annum DOE
Taking the lead in a number of fascinating clinical trials, you will perform and coordinate all aspects of the clinical monitoring process. Travelling across the UK for the purposes of on-site monitoring, you will help identify clinical trial participants, seeing to it that these patients are receiving the highest levels of care.
·Have at 2-3 years of independent monitoring experience in a pharmaceutical or clinical research organisation, with the ability to manage the full lifecycle of a trial. From start up through to close out, you’ll be a walking-talking monitoring guru.
·Have a life sciences degree & be qualified to conduct independent monitoring activities.
·Have a solid knowledge of ICH-GCP, EU and FDA requirements, and you will be comfortable using medical terminology.
·Have comprehensive medical or therapeutic area knowledge.
·Be a team-player, with an inspirational approach to leadership. As such, you’ll have great communication skills.
·Have the capacity to organise and manage your own workload, with the ability to lead the work of more junior colleagues.
·Be IT literate. Microsoft Office skills are essential, and you will be capable of learning new software.