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
- 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.
ExecuPharm a PAREXEL company is a contract research organization (CRO) that provides clinical research support services to companies from the pharmaceutical industry.
The company has more than 18,000 global clinical operational specialists in its network and it is one largest privately-owned global diversity suppliers of clinical development services since 1994.
Single sponsor dedicated to the largest biotechnology company with headquarters in the Pacific Northwest and Switzerland with 1,600+ passionate employees helping people with cancer with targeted treatment.
This position focuses on all activities required to evaluate, initiate, monitor and close clinical sites. This role may provide operational input to clinical study teams as directed.
There may also be the opportunity to contribute to other clinical trial related activities, including vendor management, data review, or other study-related in addition to identifying and qualifying potential investigators.
- Oncology TA area experience.
- BA/BS, or equivalent, or relevant experience and training with at least 4 years independent CRA Experience - all types of visits.
- Desirable: Study Start up and EC Submissions experience.
- Flexibility towards work assignments, learning, and travel.
- Able and willing to travel approximately 55-75%. Travel requirements will vary depending on study requirements, site assignments, site remote monitoring capabilities, and geographical location.
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