CLINICAL RESEARCH ASSOCIATE

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.
This is your chance to become part of a team that helps to bring miracle of medicine to market sooner.

About the Job:
• Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties.
• Ensure the integrity of the data submitted
• Recruitment of potential investigators, preparation of EC submissions, negotiate study budgets, notifications to regulatory authorities, translation of study-related documentation.
• Co-ordinate designated clinical projects as a Local Project Coordinator and may act as a local client contact as assigned.

About You:
• Ideally, a University or college degree (life science preferred)
• Have typically at least 2 years experience as a clinical monitor
• Willingness to travel between 50 – 80% of your time
• A thorough knowledge of Good Clinical Practice (GCP)

We Offer:
Covance’s ongoing success offers team members unsurpassed growth and career development opportunities.
At Covance, we help make the miracles of medicine a reality. We offer opportunities to work on diverse, challenging projects with bright, interesting colleagues while building a flexible and rewarding career.

There is no better time to join us!

Covance is committed to diversity in the workplace and is an equal opportunity employer. (M/F/D/V). Your confidentiality and privacy are important to us.


Please log onto www.covancecareers.com and search for job requisition# 23383