Clinical Research

• Support the Project Manager, traveling CRAs, and Lead CRA on clinical trials
• Ensure monitoring activities are properly supported
• Track, collect, and review critical documents
• Collect, track, and review investigational site records related to subject screening and enrollment
• Assist in developing study plans and status reports
• Collect, track, and review site regulatory documents
• Assist with developing and reviewing Informed Consent Forms
• Interact with sites, clients, vendors, and internal study team members
• Maintain the CTMS and other project tracking tools
• Track study supplies and coordinate shipments to sites as needed
• Manage the study Trial Master File and ensure periodic TMF audits
• Coordinate work with CRAs conducting on-site monitoring
• Perform on-site co-monitoring and remote monitoring activities
• Review data entered by investigational site staff according to data review and monitoring guidelines
• Assist CRAs with query resolution and data reviews
• Ensure studies operate in compliance with study protocols, Rho SOPs, ICH/GCP guidelines, and federal regulations
• Potentially mentor other team members

Explore In-House Clinical Research Associate at Rho. Review requirements and application details.