Description
Main Responsibilities:- Works under general supervision, and 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
- 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, as applicable.
- 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
- Conducts reference material testing in-house.
- Organizes investigator meetings, as necessary.
- Keeps informed of trends and developments in clinical research.
- Knows and effectively uses the broad concepts of a particular field or speicalization to resolve problems of limited scope and complexity.
- Analyzes alternative approaches to solve problems or devleop new perspectives n existing solutons.
Education: Bachelors Degree or Masters Degree, Life Sciences preferred
Experience: 2-4 years of experience required; 4-6 years preferred
Travel: Able to travel up to 30% during peek periods
To find out more about Real please visit www.realstaffing.com