Covance is seeking Clinical Research Associates (CRAs) to be office-based in Mexico City, Mexico.
Sign-on bonus is available!
COVANCE is a leading global drug development services company and we provide support to the Pharmaceutical and Biotechnology industries. You can make a difference by helping to deliver life-saving and life-enhancing medicines to people around the world. Our commitment to this mission has resulted in Covance's impressive history of company stability and growth. We've achieved these results by fostering a work environment that encourages, develops and leverages our team's capabilities.
As a Clinical Research Associate (CRA) at Covance you will be working on critical clinical trials for large, prominent pharmaceutical companies. You will conduct site monitoring responsibilities for clinical trials, according to Covance Standard Operating Procedures, ICH guidelines and GCP, including Pre-study, Site Initiation, Routine Monitoring and Close Out Visits. The CRA role will allow you will work on a close-knit team and be mentored by your Manager. At Covance, we know that career development is not one size fits all. We want you to not only succeed – but excel!
See what Covance CRAs have to say:
“The opportunities to grow are one of the top things I like about Covance. Covance really allows you to find a place to be happy. The flexibility of opportunities with Covance is just wonderful."
"One of the things that attracted me to Covance was its longstanding reputation as an industry leader. I consistently hear from sites that Covance is one of their preferred CROs to work with, which speaks volumes about the company’s reputation.”
Visit Covance's CRA microsite to learn more about being a CRA at Covance: https://inside.covance.com/careers-cra-jobs-clinical-research-associate