Are you an organized person who can work independently and take ownership of your career? Would you like to gain on-the-job skills while helping advance life-changing medicines?
If you are looking to enter a nurturing environment that provides a clear path to advancement, consider furthering your career as a Covance Clinical Research Associate (CRA). In this role, you will:
Why CRAs choose Covance
Working both field and home-based, our CRAs form strong connections with a team that works together to achieve shared success. As a CRA at Covance, you can expect to:
What we’re looking for
CRAs are the most successful at Covance with at least two years of clinical monitoring experience along with:
See what Covance CRAs have to say
“I work very hard but have a good balance. My manager is very 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."
"Clients want to work with us. I truly believe we have quality work and quality people.”
The CRA opportunity
Beyond the excellent compensation and comprehensive benefit package you'll receive as a Clinical Research Associate, joining Covance opens the door to many career opportunities. Learn more about what’s possible with a company who truly invests in you at http://covance.com/CRAcareers.
Get to know Covance
At Covance, we value your unique point of view and bold ideas to help bring innovative medicines to market and advance modern healthcare. Join our supportive team and see how our flexible work environment along with mentoring, training and career development can help you thrive personally and professionally.
Together, let’s shape new possibilities for your career and improve the lives of patients around the world.
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.
University or college degree, or certification in a related allied health profession from
an appropriately accredited institution (e.g., nursing licensure),
Master´s Degree in Clinical Research
Fluent in English
At least 2 years of experience of independent monitoring experience across phases II and III in internatioanl drug development trials