Description
Roles and Responsibilities:- Reviews study protocols, reports and manuscripts
- Works under supervision, and participates in the design, planning, implementation and overall direction of clinical research projects
- Collects and maintains legal and regulatory documentation
- Assumes responsibility for training and coordinating certification of study site personnel
- Assists, prepares and manages study timelines
- Works with Data Management and Biostatistics team on the design of documents and processes for the collection of study data from participating sites
Requirements:
- Bachelors degree in a scientific discipline or related field
- MS degree is preferred
- 4-6 years of relevant clinical research experience
- Strong working knowledge of regulations and guidelines
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Important Skills:
- Diagnostic experience is preferred
- Familiar with EDC systems (MedRio)
- Field and in house monitoring experience
- 15-30 % travel during occasional peak periods
To find out more about Real please visit www.realstaffing.com