eRecruit Assist

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

About the Job

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; Manage projects under direction of a Project Manager/Director as assigned.
Review progress of projects and initiate appropriate actions to achieve target objectives.
To organize and make presentations at Investigator Meetings.
To participate in the development of protocols and Case Report Forms as assigned.
Negotiate study budgets with potential investigators and assist the legal department with statements of agreements as assigned.
Act in the project role of as Local Project Coordinator or Lead CRA as assigned
About You

Willing to travel up to 40-50% of the time including overnight stays
Ideally 3-5 years experience as a Clinical Research Associate
Fluent in spoken/written English

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.
If you wish to apply for this position please apply directly to the Covance website www.covancecareers.com quoting ref no: 27775.