.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.
**Your time here**At Parexel, the CRA role offers the opportunity to go beyond the role of a typical clinical monitor.
CRA's are accountable for using their expertise to build and maintain the site relationship and ensure they're set up for success.
As the clinical sites' sole point of contact, this includes addressing and resolving site issues and questions.
You'll also manage site quality and delivery from site identification through to close-out.As a CRA, Parexel will offer you world class technology and training catered to your individual experience.
You can anticipate less travel and a lower protocol load in comparison to industry peers.
Your hard work may be rewarded through a **bonus incentive program**, the opportunity to work within multiple therapeutic areas and an opportunity to advance your career in clinical research.
If impact, flexibility, and career development appeal to you, Parexel could be your next home.
**What you'll do**- Leverage your expertise.
Conduct qualification visits (QV), site initiation visits (SIV), monitoring visits (MV) and termination visits (TV) at assigned clinical sites and generate visit/contact reports.- Build relationships.
Oversee integrity of the study and utilize problem-solving skills to promote rapport with the site and staff.- Drive productivity