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.
- Full Time
- Level: Mid
- 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
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Global Impact
We are one truly global team working together to propel each client´s journey ahead faster.
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Balance
We value work-life balance. We try and keep regular hours and an emphasis on life outside the office.
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Collaboration
Work with industry leaders and subject matter experts.
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Freedom
The ability to innovate, ask “what if” and try new solutions without fear of failure.
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Variety
Opportunities to work on multiple accounts – never boring!
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Compensation
Competitive salaries and bonus structure based on individual metrics.
Responsibilities
For our Client-one of the most prestigious Biopharmaceutical Companies in the world with impressive financial results for 2024-we are currently looking for an experienced CRA to join Parexel FSP on a full-time permanent contract.
Offering competitive salary with an excellent benefits package-we would like to bring on board a dedicated Individual with passion for clinical research.
CRA II will have numerous responsibilities including:
Acting as Parexel’s direct point of contact with assigned sites, accountability for quality and delivery during the start-up phase.
Assessing and ensuring overall integrity of study implementation and adherence to study protocol at clinical sites, problem-solving to address and resolve site issues.
Ensuring timely and accurate completion of project goals and updating of applicable trial management systems.
A successful candidate will have substantial Site Management experience or equivalent experience in clinical research, with understanding of clinical trials methodology and terminology. They will be educated to degree level (biological science, pharmacy, or other health-related discipline) or equivalent nursing qualification.
Parexel FSP Talent Acquisition Team will answer any additional questions you might have. We look forward to hearing from you.
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