Post-Marketing Clinical Studies Coordinator, Biologics Pioneer Surgical Technology

Responsibilities: Coordinate all post-marketing clinical studies within the Biologics group including:

- scheduling investigator meetings/site visits
- maintaining study documentation
- coordinating and assisting in site training as needed
- assist in site monitoring as needed
- assist in protocol preparation
- coordinate IRB submissions
- monitor and coordinate data collection
- coordinate studies with Pioneers Regulatory and Clinical study groups
- prepare submissions to the Pioneer clinical study committee
- coordinate study submissions for clinical meetings and publications

Requirements

- undergraduate degree in a health science with a minimum of 2 years clinical trial experience
- extremely organized and able to handle multiple projects in diverse geographic locations
- familiar with all aspects of clinical study documentation
- experience in clinical study monitoring
- experience in clinical study site training
- experience with IRB submissions
- experience creating CRFs and other study documents
- be knowledgeable about GCP
- experience working with surgeons and OR procedures

Position is located in Greenville or Raleigh, NC.

Location:	Raleigh, NC United States