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
Check out the top traits we’re looking for and see if you have the right mix.
"The last 4.5 years I had a steep learning curve and I am still learning via on-the-job challenges and solid management feedback. Next to my personal growth, I also enjoy our open atmosphere and the great collegiality."Stefanie – Sr Clinical Research Associate
We are one truly global team working together to propel each client´s journey ahead faster.
We value work-life balance. We try and keep regular hours and an emphasis on life outside the office.
Work with industry leaders and subject matter experts.
The ability to innovate, ask “what if” and try new solutions without fear of failure.
Opportunities to work on multiple accounts – never boring!
Competitive salaries and bonus structure based on individual metrics.
Parexel FSP is currently seeking Clinical Research Associates (CRA I) with 6 months of minimum experience. Homebased - Central or Northern Poland.
As a leading Clinical Research Organization in the world, we are looking to strengthen our Clinical Operations team in Poland. As a CRA you will work independently and actively handle all necessary activities required for setting up and monitoring a study, completing accurate study status reports, and maintaining study documentation. You will be involved in the submission of protocol, and consent documents for ethics/IRB approval and assist in the preparation of regulatory submissions as requested.
You will have the opportunity to be single sponsor dedicated to one of the global top 10 pharmaceutical companies, working on oncology studies that deliver real impact.
If impact, flexibility, and career development appeal to you, Parexel could be your next home.
- Bachelor's degree in a life science or related discipline.
- Minimum of 6 months of active independent field monitoring experience - all types of visits.
- Understanding of ICH GCP Compliance.
- Excellent time management and social skills
- Highly motivated with a phenomenal eye for detail.
- Ability to travel.
Benefits of working with Parexel FSP:
- Premium salary.
- Paid holidays.
- Medical care plan: Health, Dental & Vision.
- Life Assurance.
- Company cell phone and equipment.
- Market-leading PTO.
- Culture of teamwork and collaboration.
- People who motivate and face challenges together.
- Innovative technology.
- Excellent training.
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 career. In addition, you will have the opportunity to develop within your role and tackle further responsibilities or develop your skillset within other related departments of Parexel
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