At Pharmiweb, we are seeking a skilled Clinical Research Associate to join our team in the UK. As a key member of our clinical research team, you will be responsible for site management and monitoring, ensuring the highest quality standards in clinical trials.
The ideal candidate will have experience in independent on-site monitoring in the UK, with a strong understanding of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. A life science degree or equivalent industry experience is required.
You will work closely with sites to adapt, drive, and track subject recruitment plans, providing protocol and study training as needed. Additionally, you will create and maintain monitoring visit reports and action plans, and may co-monitor, train, and mentor junior members of the team.
If you are a motivated and detail-oriented individual with excellent communication skills, we encourage you to apply for this exciting opportunity.