Senior Clinical Research Associate - FSP

When our values align, there's no limit to what we can achieve.
 
At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.

Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.

Parexel is currently seeking a Senior Clinical Research Associate to support us in the UK, assigned to one of our key sponsors.

Working as a Senior Clinical Research Associate at Parexel FSP 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.

Our CRAs work from their home office base, supporting studies within their country or region. ‘Manageable sites, manageable protocols’ is our mantra. Expect exciting professional challenges in inspiring studies, but with time for your outside life.

Some specifics about this advertised role

• Dedicated to one client.

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

• Work with industry leaders and subject matter experts.

• Opportunity to mentor junior CRAs.

• Work with world-class technology.

• a pivotal role in the drug development process.

Here are a few requirements specific to this advertised role.

• 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.