Senior / Clinical Research Associate II - South West England - FSP

Responsible for all site management and monitoring activities across assigned oncology studies

Substantial Site Management experience, with an understanding of the clinical

trial methodology and terminology.

Experience in, or willingness to monitor oncology clinical trials.

Experience in independent monitoring, all types of visits.

Effective time management, organizational and interpersonal skills & problem-solving skills, with the ability to multi-task and prioritize.

Good understanding and working knowledge of clinical research, phases of clinical trials, current GCP / ICH & country clinical research law & guidelines.

We care about our people and your passion, as they are the key to our success, and provide an open and friendly work environment where we empower people and provide them with opportunities to develop their long-term careers.

In addition, you will have the opportunity to develop within your role and tackle further responsibilities or develop your skill set within other related departments of Parexel.

Working as a Senior or Clinical Research Associate II at Parexel offers tremendous long-term job security and prospects.

We undertake vital clinical studies for sponsors including the leading global biotechs and Pharma top 50. And we have an incredible pipeline of work.

Whether you see your future path as a CRA, or in fields such as clinical operations, project management, line management, or other positions, we have a world of opportunity waiting for you., Parexel supports clinical studies across the full range of therapeutic areas, and we have longstanding partnerships with a vast client base.

We supported the trials of most of today's top 50 best-selling drugs, but equally we enable more niche drug developments that are critical to the well-being of many patients.

You'll be an influential member of the wider team.