Description
Duties:- Communicates with sites regarding trial start-up, conduct, and close-out activities.
- Collects and reviews regulatory documents from clinical sites.
- Initiates, maintains, and reconciles the mail file.
- Organizes and maintains tracking systems and tools to support the conduct of a clinical study from start-up to close-out.
- Maintains accurate tracking and reporting of study metrics.
- Coordinates communication of tracking information between Operations and vendors.
- Manages and tracks study specific payments.
- Generates and reviews management reports from internal tracking systems at requested intervals.
- Coordinates investigator meeting planning, including preparing meeting materials and on-site meeting implementation.
Skills:
- Effective written and verbal communication skills.
- Good judgment in triaging calls from study sites.
- Prioritizes and multitasks to ensure that tasks are completed on time.
Education:
- Bachelor's degree and a minimum of 2 years experience in clinical research or healthcare related industry.
To find out more about Real please visit www.realstaffing.com