Research Analyst

• Contributes to the selection of potential investigators
• Accountable for study start-up and regulatory maintenance
• Trains, supports, and advises Investigators and site staff in study related matters
• Confirms that site staff have completed and documented the required training appropriately
• Ensures the sites are always inspection ready
• Actively participates in Local Study Team (LST) meetings
• Initiates, monitors, and closes study sites in compliance with Client Procedural Documents
• Updates CTMS and other systems with data from study sites
• Prepares study drug for destruction, if applicable
• Performs monitoring visits (remote and onsite)

Senior Clinical Research Associate – FSP

Senior Clinical Research Associate – Contract

Senior Clinical Research Associate I