Founded in 1979, Technical Resources International, Inc. (TRI) provides a unique range of support services in the areas of Communications, Health and Information Technology to both private industry and government agency clients. TRI is currently...

Key responsibilities include interfacing with the client and project staff, including task area managers, who oversee the day-to-day operation for multiple tasks areas with constantly shifting priorities. The multi-disciplinary project teams are...

This position will review and process essential regulatory documents received from clinical trial sites; request additional information when necessary; respond to protocol and process-related queries; maintain trial master files, and track the...

Founded in 1979, Technical Resources International, Inc. (TRI) is a full service contract research organization (CRO) providing product development support services to the global drug, biologic, and medical device community through the effective...

Founded in 1979, Technical Resources International, Inc. (TRI) provides a unique range of support services in the areas of Communications, Health and Information Technology to both private industry and government agency clients. TRI is currently...

Founded in 1979, Technical Resources International, Inc. (TRI) provides a unique range of support services in the areas of Communications, Health and Information Technology to both private industry and government agency clients. TRI is currently...

Founded in 1979, Technical Resources International, Inc. (TRI) provides a unique range of support services in the areas of Communications, Health and Information Technology to both private industry and government agency clients. TRI is currently...

Coordinating, attending and otherwise supporting Scientific Review Committee meetings. Drafting, coordinating reviews of, and distributing Scientific Review Committee Consensus Memos and/or meeting minutes/action items and responding to...

• Prepare and maintain Informed Consent Templates used to prepare Sample Informed Consents • Perform regulatory review of the protocol sample informed consent and the informed consent submitted by clinical sites • Prepare, update, and maintain lists...

This position will be responsible for conducting reviews of domestic and international sample and site-specific informed consent documents for compliance with applicable federal regulations and policies; providing expertise on the implementation of...