Clinical Documentation Specialist

Title: Clinical Documentation Specialist - C
Location: North Chicago, IL
Duration: 4 Months
Job ID: 005829

Job Description:
This position is Non Exempt. Hours over 40 will be paid at Time and a Half. Manage Phase I – IV study activities, including: participate in the development of protocols, participate in CRF design, manage drug supply, initiate and monitor sites directly or indirectly, monitor CRO activities and provide training as necessary, act as primary liaison between central IRB and sites, assist in the management of central lab, CRO and sites, assist with identification and recruitment of study sites, review and track contracts, review regulatory documents prior to drug shipment, participate and present at Investigator Meetings and other training sessions. 5+ Years Experience Level.
Required Skills:
Must have experience working in a lab environment such that the experience can be applied to the current position. The candidate must have proven experience with good technical writing skills and attention to detail. The position involves completing multiple documentation-related activities including: writing method validation protocols and reports, verification of laboratory records, preparation of data summaries, and entering information into databases. Must have experience with Microsoft Word, Excel, ChemDraw, and databases. Start date is asap.

All your information will be kept confidential according to EEO guidelines. If you believe you're qualified for this position and are currently in the job market or interested in making a change, please give me a call as soon as possible at (973) 967-3569