The Site Visit Report Reviewer (SVRR) is responsible for the review and approval of site visit reports within the timebound metrics agreed with the specific Sponsor being reviewed for or SOP agreed. Within this review and approval come the surveillance…
The Clinical SAS Programmer will lead the programming activities for various purposes including SAS Data Listings to be used for data review, Safety Review Listings, Centralized Monitoring Listings and Reports. The Clinical SAS Programmer will also be responsible for production…
The eCOA and RTSM Application Specialist is responsible for supporting the design, deployment, configuration, and oversight of electronic Clinical Outcome Assessment (eCOA) solutions—including ePRO, eConsent, and other patient centric electronic data capture tools— and of Randomization and Trial Supply Management…
The Project Assistant works with Project Managers, Project Coordinators and Clinical Research Associates (CRA) at many stages during clinical studies. Works independently to coordinate and manage study deliverables and administrative tasks, as required by the project team. More specifically, the…
The Power BI Developer is responsible to design proper data models that support business analytics, proper workspace management, governance, data security, source code management and Power BI (PBI) administration. The Developer leverages best practices for developing high quality datasets and…
The Project Assistant works with Project Managers, Project Coordinators and Clinical Research Associates (CRA) at many stages during clinical studies. Works independently to coordinate and manage study deliverables and administrative tasks, as required by the project team. More specifically, the…
The Power BI Developer is responsible to design proper data models that support business analytics, proper workspace management, governance, data security, source code management and Power BI (PBI) administration. The Developer leverages best practices for developing high quality datasets and…
??Centralized monitoring is an integral part of a risk based monitoring strategy, defined as the timely, remote review of accumulating subject and operational data to help distinguish between reliable and unreliable data, trends, outliers, and unusual variability using analytics and…
The Senior Clinical Data Coder is primarily responsible for leading and overseeing activities related to the coding of clinical data across multiple ongoing studies. In addition to performing accurate coding tasks, the Senior Coder takes ownership of the coding module…
The Clinical Systems Specialist is responsible for providing support to internal end users for the Clinical Systems including training, troubleshooting, reporting, and managing user access. More specifically, the Clinical Systems Specialist: Manage and support the Clinical Systems, including system implementation,…