Description
A leading Pharmaceutical company, located in Illinois, is in need of an in-house CRA. The company is focused on developing innovative technologies and products that will increase patient care and quality of life.The Clinical Research Associate will have the following responsibilities:
- Responsible for conducting Phase I-IV single or multi center studied according to Federal Regulations and ICH guidelines
- Assist senior staff in planning study conduct and designing case report forms
- Assist senior staff in selecting and managing contract research organizations (CROs)
- Assist senior staff in selection and training of investigator sites, planning and running study meetings, evaluation, selection and training of new study investigators and writing and assembling submissions
- Responsible for writing basic study protocols and monitoring or overseeing monitoring of investigational sites to ensure protocol adherence
- Assure timely enrollment of patients and retrieval of CFR's from study sites, processing CRFs including data cleanup and classification of data, and completion of study summary
- Responsible for setting up and managing Clinical Research Committees
The Clinical Research Associate must meet the following requirements:
- B.S.
- 3-5 years experience as a Clinical Research Associate within a Pharmaceutical company
- Experience managing teams of 3-5
- Experience selecting and working with contract research organizations (CROs)
- Working knowledge of MS Office and MS Sharepoint
- Excellent communication skills
- Detail oriented
This is a 13 month contract, the rate is $30/hour. If you are interested please apply now or contact Dana at .
To find out more about Real please visit www.realstaffing.com