X, LLC

Analyst

• Independently translate eligibility criteria and query for patient cohorts using TriNetX LIVE™
• Apply standard coding schemes (ICD, CPT, SNOMED, etc.) to define patient cohorts based on provided criteria
• Deeply understand nuances of clinical trial eligibility criteria and represent them using available clinical data sources
• Lead live demos and training sessions to existing and prospective users of TriNetX LIVE™ with minimal oversight
• Serve as primary contact for pharma, biotech, CRO, and healthcare organization clients to identify, analyze and interpret data relevant to clinical questions and needs, and provide consultative assistance via written, oral, or in-person presentation methods
• Handle a high volume and complexity of daily questions from pharma and healthcare organization users regarding platform and analytic capabilities
• Manage multiple simultaneous customer engagements using effective workload management and prioritization capabilities
• Collaborate with the Clinical Feasibility & Analytics team and other Client Delivery staff on project evaluations, disease/study reports, and presentations
• Document and escalate feedback on product usability and potential new features to senior team members
• Support the sales and training processes of TriNetX on both the healthcare organization and sponsor (pharma/CRO) user ends of the platform
• Participate in and lead team meetings, training sessions, and knowledge-sharing initiatives to build expertise in real-world evidence and clinical operations
• Contribute to scientific publications and external conference presentations
• Mentor newer Analysts and junior team members, providing technical and professional guidance
• Track task statuses against specified timelines
• Assure data quality, integrity, and confidentiality of information
• Review professional journals and publications to help solve complex research questions and keep informed of current trends

Senior Clinical Study Analyst

Student

• Monitor and review clinical research data for accuracy, completeness, plausibility and consistency
• Ensure compliance with study protocols and regulatory guidelines
• Identify and resolve data discrepancies or issues in a timely manner
• Verifying the accuracy of all rules within the data capture system by entering test data
• Communicate with study sites and data managers to address data quality concerns
• Review data management plans
• Assist in the development and implementation of data quality assurance processes
• Support in generating reports and presentations on data monitoring activities for internal and external stakeholders
• Resource planning and co-ordination of all monitors in consultation with head of project management
• Manage site administration activities and maintain records
• Work in interdisciplinary teams with (but not limited to) project management, data management, data operations, medical advisor, pharmacovigilance
• Support in training monitors (in conjunction with PM, DM and Medical Advisor)
• Support in setting up and testing electronic questionnaires /documentation forms
• Support in pharmacovigilance related activities
• Management of participants in medical data collection surveys
• Assisting adherence to quality standards, project requirements, and compliance regulations throughout the project lifecycle
• Support in process optimization and revision of SOPs and work instructions

Student Worker, Data Monitor

Project Manager

• Own end-to-end delivery of an assigned portfolio of EU Commission and regulatory-funded projects, from kick-off through final reporting and closeout.
• Develop and maintain integrated project plans, work breakdown structures, milestone schedules, and risk registers across concurrent projects.
• Apply the Project Monitoring & Controlling SOP and RYG status frameworks to track progress, surface variances early, and drive corrective action.
• Coordinate internal workstreams and client-facing teams to ensure on-time, on-scope delivery.
• Ensure full compliance with EU grant regulations including EC Grant Agreements, General Conditions, and applicable Financial Regulations.
• Oversee preparation and submission of periodic technical and financial reports to the European Commission and other funding bodies.
• Serve as the primary point of contact for Project Officers, coordinators, and external auditors; manage responses to audit queries.
• Manage relationships with consortium partners including academic institutions, hospitals, SMEs, and other industry stakeholders across EU member states.
• Represent TriNetX at funder review meetings, project review boards, and relevant EU-funded events.

Senior Clinical Study Analyst

Student Worker, Data Monitor

Senior Project Manager