Clinical Research Associate I (FSP)

Parexel FSP is currently seeking Clinical Research Associate I

home-based, United Kingdom.

Working as a 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 on 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. Great opportunities to travel, work from home, meet new people and play a pivotal role in the drug development process.

Clinical Research Associates at Parexel FSP

Parexel FSP supports clinical studies across the full range of oncology and non-oncology 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. On a human level, if you’re a CRA with a passion for a particular therapeutic area, we’ll do our best to accommodate you. Or equally, we can help you broaden your experience.

QualificationsHere are a few requirements specific to this advertised role. Substantial Site Management experience, with an understanding of clinical trials methodology and terminology Experience monitoring oncology clinical trials or willing to monitor oncology 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.

Not quite the CRA role for you?

Don’t worry we need CRAs for different locations, sponsors, and therapeutic areas, and at entry, mid and senior levels.

Join Our Talent Community and we’ll reach out with job alerts when positions that match your career interests become available. We’ll also share periodic updates about the latest company news and events. Sign up today https://jobs.parexel.com/functional-service-provider

#INFSP