Sr. Clinical Monitor

erts and institutions powers every project we deliver—enabling collaboration, scalability, and measurable results.
• 270+ Cardiovascular Specialists
• 100+ Signed Data Sharing Agreements
• 3+ New Sites per Month
• 4 Countries represented
About

The Role

The Sr. Clinical Monitor performs site monitoring and site management activities to assess the progress of projects at assigned investigative/physician sites (either on site or remotely) and ensures clinical studies are conducted, documented, and reported in accordance with the clinical protocol, HRCRS and Sponsor Standard Operating Procedures (SOPs), ICH‑GCP and/or all applicable local and federal regulatory requirements. The Sr. Clinical Monitor represents clinical monitoring on assigned Study Teams, under the oversight of the Clinical Operations Manager and the Project Manager, providing operational expertise and functional leadership to project CRAs/Monitors performing study activities.

This role is also responsible for assessing clinical trial site performance and the effectiveness of monitoring activities through monitoring visit report review and metric tracking; communicating issues, risks and mitigation strategies to the Project Manager and Clinical Operations Manager; and contributing to the development and maintenance of study‑level documentation.
What You’ll Do
• Conduct review of monitoring visit reports and associated visit deliverables; evaluate site compliance, escalates identified noncompliance per project plans, and contributes to corrective and preventative action planning.
• Perform tracking activities for monitoring visit scheduling, performance, and completion of monitoring visit deliverables to ensure compliance with project plans and HRCRS SOPs.
• Construct or contribute to the construction of project documentation including project plans, monitoring visit tracking tools, visit reports, and site and/or CRA training materials, as requested by Project Management or Clinical Operations Manager.
• Assist with CRA/Monitor study coordination, training, and mentoring via co‑monitoring activities and meeting conduct.
• Perform senior‑level monitoring oversight across studies/sites, including site qualification, site initiation, interim monitoring, site management activities and close‑out visits, on‑site or remotely, ensuring regulatory, ICH‑GCP, monitoring plan and protocol compliance.
• Provide strategic site management and escalation, proactively identifying site‑ and study‑level risks through analysis of monitoring findings, study metrics, KRIs, and site performance trends; partner with Project Management and cross‑functional stakeholders to implement mitigation and corrective/preventive actions aligned with the monitoring plan.
• Proactively identify site and study‑level risks through analysis of monitoring findings, study metrics, and site performance trends and collaborate with Project Management to implement mitigation strategies in alignment with the monitoring plan.
• Conduct risk‑based monitoring activities including source data verification review of appropriate site source documents and medical records. Verify the required clinical data entered in the case report forms are accurate and complete and utilize query resolution techniques remotely and on‑site.
• Verify site informed consent process is adequately performed/documented for each subject.
• Routinely review the Investigator Site File for accuracy, timeliness and completeness.
• Reconcile the ISF with the Trial Master File and collect any outstanding documents.
• Serve as primary point of contact with study site personnel. Document all activities and communications with the site via confirmation letters, follow‑up letters, monitoring visit reports, communication logs and other required project documentation. Follow…