Research Assistant

Come join our growing team in Jackson, TN!

Perform a variety of research, database, and clerical duties of a complex and technical nature in support of clinical trials to ensure adherence to protocols and quality of information received.

DUTIESANDRESPONSIBILITIES

• Participate in ongoing clinical and study-specific training
• Participates in visits conducted by monitors and SIV as
• Responsible for compiling source documents for active studies and ensuring source binders contain the appropriate documentation to screen upcoming patients.
• Responsible for assisting in EDC completion
• Takes part in site and/or company team meetings as needed
• Perform all activities in compliance with Quality standards (SOP's, training, ) at the site level
• Assist in ensuring all project timelines and deliverables are met as scheduled
• Responsible for processing and shipping labs- lATA This can include pick up/drop off of certain items near site location.
• Protects confidentiality of any and all sensitive information related to HIPPA and sponsor guidelines
• Assist in ensuring that study materials and lab kits are shipped and resupplied as requested
• Conducts all work in accordance with Good Clinical Practices (GCPs), CRS Standard Operating Procedures (SOPs), and principles set forth in the CFR and !CH guidelines
• Participates in audits (internal or external) at the assigned site, as needed
• Communicates, as necessary, with the vendors and supporting functions at the site level
• Maintaining a working knowledge of Clinical Conductor
• Responsible for on-call rotation (personally being on-call for assigned rotation time frame)
• Any other task assigned by the direct supervisor and assist the site team