Clinical Research Associate - United States

Clinical Research Associate – US

In a year when medical trials have the deep interest of absolutely everyone on the planet, there’s never been a better time to consider your options. You want to join a company that values their employees. You want to be involved in the most stimulating work. And you want to be surrounded by people who are experts in their field. Well happily, our client ticks all these boxes. And then some. As a global contract research expert, this is an organisation with a strong pipeline of the most interesting and niche trials. Behind those trials, are some of the biggest and most innovative sponsors – making for a truly glorious combination. So, what can you expect when you join them as a CRA? First up, there is a real culture of support, with senior colleagues committed to your development, all underpinned by sector-leading training opportunities. Secondly, you will have the opportunity to work on cutting edge Oncology studies, working with a team that develops and delivers bold clinical programmes. Thirdly, you will receive a highly competitive benefits package that includes a leading base salary, Health and Medical benefits, along with a host of additional flexible benefits. If you are hungry to achieve more in your career, then this is the place to do it.

The role:

Taking the lead in several fascinating clinical trials, you will perform and coordinate all aspects of the clinical monitoring process. Travelling across US 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. Whilst the practical aspect of a this CRA role is an essential part of this opportunity, so too is the fact that you will be interacting daily with study sites to support the delivery of the most cutting-edge projects, including reviewing, and analysing high volumes of data. As an inspirational leader to junior colleagues, you will be keen to share knowledge and expertise, organising their workloads and seeing to it that trials for sector-leading pharmaceutical and biotech companies are meeting expected goals. With access to the most innovative clinical programmes across a wide array of therapeutic areas, this is a valuable opportunity to establish your reputation in a rapidly growing (and award-winning) organisation.

You will:

• Have 3+ years of independent monitoring experience in a pharmaceutical or clinical research organisation, with the knowledge of the full lifecycle of a trial.
• Have a life science degree.
• Have a solid knowledge of ICH-GCP 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 will 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. 

This is a fantastic opportunity to join a company who are committed to growing their organisation in the US and you will be joining a supportive team of established CRAs across the country. If you are interested in finding out more about the company, the compensation package and all the other important elements, please apply or reach out to me directly using my below details.

Alex Goodman – Clinical Research Talent Consultant

Email: alex.goodman@rbwconsulting.com