Field Clinical Research Associate 2

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 on inspiring studies, but with time for your outside life.

Some specifics about this advertised role

Opportunity to be part office based if preferred (country dependant). Dedicated to one client. Truly seen as the sponsor representative on site. 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.

You’ll be an influential member of your study team. Evaluating, monitoring, and closing sites. Involved in recruiting strategies. Protecting patients. Ensuring safe, efficient, compliant delivery.

Beyond this, there are opportunities to take part in aspects of study and project management, such as team and vendor management.

As well as learning by osmosis from industry-leading professionals, you’ll gain world class training from Parexel and from our sponsors too.

And you’ll be able to share knowledge and ideas with a global community of clinical operations, biometrics, regulatory, medical writing, and medical affairs specialists.

As you close one site, there’ll be many more opportunities open to you, at the top of your profession.

We value work-life balance. We aim to keep regular hours and an emphasis on life outside the office. We’ll value your welfare just as highly as that of our patients. Our managers will listen to, and act on, any concerns.

QualificationsMore about you

On your first day we’ll expect you to have:Site Management experience or equivalent experience in clinical research, with understanding of clinical trials methodology and terminology.Bachelor’s or equivalent degree in biological science, pharmacy or other health related discipline would be ideal.Strong interpersonal, written, and verbal communication skills within a matrixed team.Experience working in a self-driven capacity, with a sense of urgency and limited oversight. A client-focused approach to work and flexible attitude with respect to assignments/new learning.The ability to manage multiple tasks, evaluate a variety of unpredictable scenarios and achieve project timelines while being able to apply your understanding of study protocol(s).An honest and ethical work approach to promote the development of life changing treatments for patients.Strong computer skills, including but not limited to the knowledge of a Clinical Trial Management System (CTMS), Electronic Document Management System (EDMS) and MS-Office products such as Excel and Word.

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