Description
Primary Responsibilities:- Ensure studies are carried out according to ICH/GCP regulations
- Execute high-quality, integrated, cross-functional plans for assigned clinical trials
- Assist in planning and execution of clinical projects while adhering to budget, scope, and timeline requirements
- Particiapte in site selection and management from start-up through close-out
- Manage CRO / vendor relationships
- Monitor or co-monitor clinical sites as required (up to 20% travel may be required)
Skills / Education:
- Bachelors Degree minimum education requirement
- Position requires 4+ years direct clinical trial management experience, preferrably within oncology
- Field monitoring background
- Proficient with MS Word and Excel
- Excellent verbal and written communication skills in English
To find out more about Real please visit www.realstaffing.com