Senior Cra or Craii

4 weeks ago


Remote, United Kingdom Parexel Full time

Everything we do has the potential to impact patient lives, and our Clinical Research Associates (CRAs) take their work seriously, demonstrate empathy, and act with heart. They also perform with urgency, navigating our streamlined clinical operating model to drive effectiveness, reduce handoffs and increase employee, client and site satisfaction.

As a CRA at Parexel, you‘ll be joining a team with a wide variety of experiences and knowledge. We’re looking for people like you to take the initiative to do things better and smarter—people who want to grow personally and professionally. We recognize and uphold the importance of all people, the way we do things, our quest for innovation, and most importantly, our patients. Explore opportunities within our core Clinical Development, Biotech, or Functional Service Provider (FSP) teams below.
- Full Time
- Travel: Yes
- Glassdoor Reviews and Company Rating

**Success Profile**:
Check out the top traits we’re looking for and see if you have the right mix.
- Innovative
- Problem-Solver
- Communicator
- Tech-Savvy
- Confident
- Independent

**Rewards**:

- **Global Impact**: We are one truly global team working together to propel each client´s journey ahead faster.
- **Balance**: We value work-life balance. We try and keep regular hours and an emphasis on life outside the office.
- **Freedom**: The ability to innovate, ask “what if” and try new solutions without fear of failure.
- **Variety**: Opportunities to work on multiple accounts - never boring
- **Compensation**: Competitive salaries and bonus structure based on individual metrics.
- Additional Job Description

**Parexel FSP is currently seeking a Senior Clinical Research Associate or CRAII Up to 0.6 FTE. Home-based - South West, UK.**

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 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

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.

**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.

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 long-term 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 FSP.

For an immediate interview please contact the job poster.

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