Description
Responsibilities:- Participates in the design, planning, implementation and overall direction of clinical research projects
- Travels to field sites to monitor studies
- Reviews study protocols, reports and manuscripts; contribute technical and clinical operations expertise for these documents
- Collects and maintains legal and regulatory documentation
- Ensures accurate and complete study management/data collection and transfer to data mangement
- Assists, prepares and manages study timelines
- Organizes investigator meetings, as necessary
Requirements:
- Bachelors degree in a scientific discipline or related field, or equivalent combination of education and work experience; MS preferred
- 4-6 years of relevant clinical research experience
- Travel approximately 30% of time
- Prior laboratory experience preferred
To find out more about Real please visit www.realstaffing.com