In House Clinical Research Associate

Join our global team dedicated to innovation and initiative, where physical walls and different time zones don't limit, but encourage, collaboration. As an In-house Clinical Research Associate, you will manage and support clinical sites from site approval through close-out, ensuring the integrity of the trial data without the need for frequent travel.

Requirements

• Develops study documents and tools
• Supports sites in obtaining IRB approval
• Ensures all required site regulatory documents and approvals are in place prior to investigational product shipment
• Maintains regular communication with study sites
• Conducts remote review of data entered on electronic Case Report Forms (eCRFs)
• Works closely with field CRAs and data management to resolve queries on discrepant data

Benefits

• Generous Paid Time Off
• 401k Matching
• Retirement Plan