Remote Site Monitor (Central)- RRS
Responsibilities:
• Performs review of clinical monitoring visit reports ensuring consistency across protocols and/or regions and escalates any protocol, site, and/or CRA issues or trends noted during the report review process to CTM.
• Liaises with CRA for prompt trip report review submission and approval as per the stipulated timelines of PPD and/or the Sponsor.
• Evaluates PI oversight (e.g., protocol adherence), subject safety and study processes in order to assess site’s ability to conduct study, as ascertained from information noted in monitoring visit reports and associated electronic data systems.
• Provides trial MVR status tracking and progress update reports to CTM/CRA as required.
• May assist project manager or clinical team manager on assigned projects.”