Clinical Research Associate (CRA)
Work Location: Des Plaines, IL (Hybrid, for Local) or Remote
Contract: 12 months
Note:
- Must be vaccinated and able to travel 25-30%.
- May need to travel internationally as well.
Role and Summary:
Member of the clinical team responsible for conducting Phase I-IV single or multi center studies according to Federal Regulations and ICH guidelines. Responsible for assisting senior staff in planning study conduct, designing case report forms (CRFs), Contract Research Organization (CRO) selection and management, 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, monitoring or overseeing monitoring of investigational sites to ensure protocol adherence, assuring timely enrollment of patients and retrieval of CRFs from study sites, processing CRFs including data cleanup and classification of data, and completion of study summar
Required:
5+ Years related experience
Job Types: Full-time, Contract
Salary: $35.00 - $40.00 per hour
Benefits:
- Dental insurance
- Health insurance
- Vision insurance
Schedule:
- 8 hour shift
- Day shift
- Monday to Friday
Education:
- Bachelor's (Preferred)
Experience:
- Clinical Research Associate: 5 years (Required)
- Medical Device/Pharmaceutical/equivalent industry: 3 years (Required)
Willingness to travel:
- 25% (Required)
Work Location: Remote
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