Clinical Trial Monitor

Hurley Consulting Assoc.
Summit, NJ
Sep 25, 2018
Required Education
Bachelors Degree
Position Type
Full time

Clinical Trial Monitor

BA/BS with at least 3 year's pharmaceutical industry experience, an RN a plus. 

Experience in central monitoring.

Oncology experience a plus.

Site set up activities, the collection of regulatory documentation. 

Review data, raise and resolve queries at the site and perform source data verification.

Assist in the design of case report forms and edit checks.

Responsible for central monitoring.

Responsible for coordination of site monitoring activities. 

Responsible for interaction with Biometrics staff for database lock.

Familiarity with EDC software.

20-30% travel. 

In-House, Permanent opportunity. No relocation benefits offered at this time.

Competitive salary and benefits package which includes medical, dental, vision, group life insurance and matching 401(k).