Description
Main responsibilities include but not limited to:- Particpates in the design, planning, implementation and overall direction of clinical research projects
- Travels to field sites to monitor studies (up to 30% travel, all within the US)
- Reviews study protocols, reports and manuscripts
- Works with Data Management and Biostatistics staff on the design of documents and processes for the collection of study data from participating sites
- Collects and maintains legal and regulatory documentation
- Assumes responsibility for training and coordinating certification of study site personnel
- Ensures accurate and complete study management/data collection and transfer to data management
- Ensures site compliance with regulations and study protocol
- Monitors the sites and provides technical assistance, as necessary
- Assists, prepares and manages study timelines
- Manages material logistics for the studies
- Keeps informed of trends and developments in clinical research
Education / Experience Required:
Must have a Bachelors Degree in a scientific discipline, Molecular Biology degree preferred. Candidates with prior clinical laboratory experience / experience as a research associate strongly desired. Must have 2-4 years experience as a Clinical Research Associate within the Medical Device, Pharmaceutical, or Biotech industry; must have clinical monitoring background.
This position is 40 hours per week with potential extensions beyond 18 months.
To find out more about Real please visit www.realstaffing.com