Study Start Up Associate I

At ICON, it's our People that set us Apart"

Are you interested in improving your knowledge of Clinical Trials and contributing to our culture of process improvement with a focus on streamlining our processes of adding value to our business and meeting client needs?

Study Start Up Associate l role within ICON:

Selected to coordinate clinical trial start-up activities and serve as primary contact for investigators and research coordinators in corporate sponsored human clinical trials.

The successful candidate will show capability in the areas of Clinical Trial operations, meeting regulatory and ICON guidelines and displaying project management skills.

We are presently in over 40 countries with over 80 offices worldwide and over 13K employees globally.  We are comprised of 6 divisions and offer a full-service portfolio of solutions to our clients. 

Benefits of working at ICON:

We provide a Study Start Up Associate with the resources to be successful and visibility by having them provide input and recommendation to upper management on the study start up submission process and how to better the work process. In addition, we offer excellent health, dental, vision and life insurance coverage; 401(K) with company match; competitive pay; generous time off; and bonus incentives

Minimal travel may be required (10%)

To succeed you will need:

A high school diploma or local equivalent, Bachelor’s Degree preferably in life sciences will ensure your familiarity with regulatory guidelines and industry knowledge. Minimum of 1 year of experience or understanding of clinical study start up requirements and activities.

What’s Next?

Following your application you will be contacted by one of our dedicated recruiters and if successful we will be able to provide you with more details about this opportunity.

ICON is an equal opportunity employer - M/F/D/V and committed to providing a workplace free of any discrimination or harassment.