Research Analyst

• Perform on-site and remote monitoring visits to ensure subject safety and data quality
• Review CRFs and source documentation for accuracy and completeness
• Ensure informed consent procedures and protocol compliance are met
• Manage and track Investigational Product accountability
• Prepare monitoring visit reports and follow up on action items
• Maintain and update eTMF, CTMS, and trial documentation systems
• Support sites with issue resolution and ensure timely completion of deliverables
• Participate in audits and inspections, including preparation and follow-up
• Collaborate with project teams and contribute to monitoring plans, project tracking, and CRA resource planning

Senior Clinical Research Associate

• Conducting thorough research into an individuals’ background using a variety of tools, such as databases and public records
• Gathering information, analyzing data, and compiling this information to be entered into a final report
• Processing searches related to background screening reports
• Ensuring all searches are processed and reported according to state and federal laws as outlined in AccuSourceHR’s reporting guidelines
• Ensuring all searches are processed according to client guidelines
• Retrieving public records information and entering said information into our platform
• Analyzing information and comparing data sets to confirm matching identifiers
• Performing other duties as assigned
• Meeting or exceeding minimum standard service requirements

Research Analyst jobs in New Hampshire

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Senior Clinical Research Associate

Research Specialist