Clinical Studies Specialist

Clinical Studies Specialist needed in North Chicago Illinois suburb.

Compensation is commensurate with experience.

This position requires 5+ years experience. The slected individual will be a member of the clinical team responsible for conducting Phase I-IV studies according to Federal Regulations and ICH guidelines. This person will provide strong support of the clinical team; Assist Clinical Team members in handling data queries, drug inventories, study invoice payments, enrollment tracking, and record reconciliation with site documents; Assists the CRA's with organizing and plannning study investigator meetings and preparing presentations.

Additional Experience Requirements:

* Experience reviewing clinical research regulatory documents i.e. FDA form 1572, CV?s, financial disclosures
* Knowledge and experience in drug development process and regulatory requirements
* Computer proficiency in an email program (Lotus Notes preferred), MS office suite, e-submission software (documentum preferred), web page design software application also desirable i.e. MS FrontPage
* Excellent communication skills, written and verbal. Ability to work in a matrix environment is required.

Education Requirements: AS/BS Preferred.