Description
Responsibilities:- Assist in managing all aspects of clinical studies at Anthera to ensure studies are completed on time, within budget and in compliance with SOPs, FDA regulations and ICH/GCP guidelines
- Perform the activities of planning, implementing, monitoring and the management and tracking of clinical trials
- Assist in the supervision of internal Clinical Support Team and Contract Research Organizations
- Work with data management to resolve data discrepancies
- Assist in the preparation of clinical study reports and annual reports
- Participate in the design and development of clinical trial protocols and case report forms
Requirements:
- Bachelor's degree in a scientific discipline or health-related field preferred
- 3+ years as a Clinical Research Associate
- Demonstrated management of CRAs and Contract Research Organizations a plus
- Willingness to travel (up to 50%) as necessary, consistent with the project needs
- Ability to work quickly and accurately in a fast-paced environment
To find out more about Real please visit www.realstaffing.com