CTA w/experience

 erik.lombere@lombereindustries.com

CTA need with sponsor and/or CRO experience. This would be near full time hours for at least 6 months, fully remote. Pays up to $50/hr depending on experience. 

Assist with reviews of study-specific essential regulatory document packets prior to site activations
Assist with the negotiation, review, and approval of investigator site contracts and budgets
Coordinate and conduct Sponsor review of ICFs
Assist with investigator site feasibility assessment
Assist CTM with Vendor Management activities, independently manage ancillary vendors (e.g. recruitment, travel concierge, home nursing)
Perform site management activities per assigned study (s)
Establish and maintain sponsor, vendor, and site relationships
Assist with and provide input into the preparation of site and study-related documents, tools, and templates (e.g. start-up forms, screening scripts, source documents, study logs)
Record meeting minutes and provide agendas to the clinical operations team, as needed
Provide support and participate in clinical trial systems specification development and testing
Update internal and external systems in a timely manner and assist with the maintenance of the Trial Master File.