Description
The Senior Clinical Research Associate participates in the design, planning, implementation and overall direction of various clinical research projects under general supervision. Main responsibilities include:- Travel to field sites to monitor studies (20-30% max travel, locally)
- Review study protocols, reports, and manuscripts and contributes clinical operations expertise for these documents
- Works cross-functionally with various departments 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
- Organizes investigaor meetings, as necessary, and participates in Project Team Meetings
- Ensures accurate and complete study management / data collection and ensures site compliance with regulations and study protocol
- Conducts reference material testing in house
- Analyzes alternative approaches to solve problems or develop new perspectives on existing solutions
Education: Bachelors degree in a scientific discipline or related field, or equivalent combination of education and work experience. Masters Degree preferred.
This position requires 2+ years of clinical monitoring experience. Prior experience working as a CRA for a medical device or diagnostic company highly desirable.
To find out more about Real please visit www.realstaffing.com