Sevices

ReSQ Clinical Research Associates (CRAs) are available on an 'as needed' basis to support the monitoring of Phase I to Phase IV studies from inception to close out. All ReSQ CRAs have extensive experience and have worked in senior clinical research, quality or training roles.

 

In addition, ReSQ provides support in:

• Protocol development
• Project management
• Pharmacogenomics and DNA banking approval and processes
• Writing of Standard Operating Procedures (SOPs)
• Clinical support in CRF design
• Medical and technical writing
• Feasibility studies
• Auditing
• Co-monitoring
• Animal health studies
• Mentoring and coaching