Clinical Research Associate II or Senior Clinical Research Associate Oncology - Midlands UK - FSP

When our values align theres no limit to what we can achieve.

At Parexel we all share the same goal to improve the worlds 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 were committed to making a difference.

Parexel is currently seeking a Clinical Research Associate either level II or Senior for a role in the Midlands. This will be dedicated to one sponsor.

Working as a Clinical Research Associate at Parexel FSP offers tremendous longterm 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 worldclass 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 & problemsolving skills with the ability to multitask 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 longterm 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.

Who are Parexel

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 todays top 50 bestselling but equally we enable more niche drug developments that are critical to the wellbeing of many patients.

Youll be an influential member of the wider team.

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