Technical Resources International Jobs in United States

DescriptionThe Safety Associate is essential for collecting, organizing, and interpreting data accurately to support project-specific safety operations. The Safety Associate focuses on managing and analyzing safety-related data under supervision  · Responsible for ensuring data a ...

DescriptionOversight of clinical operations activities, including one or more of the following: clinical project management, clinical site management (essential regulatory documents, study start up, site monitoring), and/or clinical systems management (CTMS, TMF documentation rev ...

Job Title · Regulatory Operations Associate · Location · Bethesda, MD 20817 US (Primary) · Category · Regulatory Affairs · Job Type · Full-Time · Salary Range · 54, ,000.00/YEAR · Education · Bachelor's Degree · Travel · None · Job Description · Prepare standard documentation sup ...

DescriptionResearches and identifies new opportunities and/or prospective clients in support of clinical research, communication, and IT services. · Supports the preparation of proposals by coordinating cross-functional teams, conducting research, and liaising with vendors. · Wri ...

Job Title · S & P Specialist · Location · Bethesda, MD 20817 US (Primary) · Category · Drug Safety · Job Type · Full-Time · Salary Range · 70, ,000.00/YEAR · Education · Master's Degree · Travel · None · Job Description · Ensures compliance with TRI Standard Operating Procedures, ...

DescriptionPerform needs assessments, strategic learning assessments, and other studies to focus learning needs and form the basis for curriculum development. · Design and develop training plans including learning objectives, course outlines, case studies, measurement tools, stud ...

DescriptionPrepare standard documentation supporting regulatory filings and distribution to stakeholders. · Utilize and maintain hard copy and electronic filing systems for auditable regulatory documents. · Maintain effective high-profile communications and interactions with coll ...

DescriptionPrepares scientific and regulatory documents on behalf of government and private sector clients for submission to the Food and Drug Administration (FDA) (Investigational New Drug applications, annual reports, preclinical and clinical study reports, safety reports, and ...

DescriptionSupports the maintenance and upkeep of the Quality Management System (QMS).  · Maintains the Quality Assurance (QA) training program, document control, deviation program, and CAPA program.  · Supports performance metrics system for continual improvement.  · Manages the ...

DescriptionEnsures compliance with TRI Standard Operating Procedures, Food and Drug Administration and World Health Organization regulations and global regulations for the reporting of adverse events to regulatory agencies · Develops and ensures the uniform and timely processing ...