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Clinical Research Associate (CRA)

Job Category: Clinical Research Associate
ID: 70620BR

Job Description

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 values a WORK / LIFE BALANCE!

- Unlike some CRA roles you will not be pushed to satisfy unrealistic ‘monthly visit’ targets
- Training and development, both initially and throughout your career
- Join a company where people tend to stay for 6-10 years rather than 1-3!
- Join a genuinely friendly and supportive company where they allow individuals to take ownership of their own performance.

See what Covance CRAs have to say:

“I work very hard but have a good balance. My manager is super supportive and in tune to my professional development.”

"I have really enjoyed working with my colleagues to accomplish project objectives and can see that what I do has an impact on the success of this company."

"People want to work with us. I truly believe we have quality of work and quality of people.”

Visit Covance's CRA Microsite to Learn more about being a CRA at Covance

Education/Qualifications

• University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing licensure)
• Valid Driver’s License

Key words: Clinical Research, CRA, SCRA, Clinical Research Associate, GCP, Monitor, Monitoring, Senior Clinical Research Associate, CRA I, CRA II, CRA III, LCRA, Oncology, Cardiovascular, Neuroscience, Immunology, Infectious Diseases, Metabolism, Field Based, Home Based, CRO, Pharmaceutical

Experience

• 2 years of Clinical Monitoring experience.

EEO Employer

Covance is committed to diversity in the workplace and is an equal opportunity employer (Minority/Female/Individual with Disability/Veteran/Sexual Orientation/Gender Identity). Your confidentiality and privacy are important to us.
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