Covance is seeking Remote Clinical Research Associates (CRAs) across the US! Up to a $15k sign-on 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. As a CRA, 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 to excel!
Successful candidates will enjoy the benefits of working for a company that
Responsibilities and Duties
Clinical research associates must be highly organized with strong analytical, research, math and statistical skills. They should be good problem-solvers with a solid understanding of scientific data collection and management methods. Solid verbal and written communication skills are necessary, as is the ability to interact with healthcare professionals, researchers, clinical trial sponsors and trial participants. Excellent computer skills and proficiency with spreadsheets are essential. Multiple language skills may give an applicant an advantage with certain employers.