Description
Primary Responsibilities:- Travels to field sites to monitor studies (up to 30% during peak periods)
- 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
- Assists, prepares and manages study timelines
- Conducts reference material testing in-house
- Organizes investigator meetings, as necessary
- Participates in Project Team Meetings
- Keeps informed of trends and developments in clinical research
Requirements:
- 4-6 years of relevant clinical research experience as a CRA
- Bachelors degree in a scientific discipline or related field, Masters Degree preferred
- Detail oriented "people-person" with excellent lab skills
- Excellent communication skills, both verbal and written
- Ability to handle problems, meet timelines and manage sites
- Analyzes alternative approaches to solve problems or devleop new perspectives on existing solutions
To find out more about Real please visit www.realstaffing.com