Clinical Trial Rx
Clinical Trial Rx
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start the process of rescuing Clinical Trials & RWE/RWD Studies away from The underachieving CRO

Our Value Proposition 

"Right the First Time, On-Time, On-Target"

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Failing CRO RESCUE SERVICE offerINGS

Central Lab Rescues

Project Management Rescues

Project Management Rescues

 Remove the risks of NDA Submission delays and failures caused by Central Lab CPM SOW set-up errors, data delivery failures, and budget overruns. CTRx understands the frustration of Study Sponsors learning that a Phase III Pivotal Clinical Trial has 78,000 patient samples LOST, PENDING, or on HOLD one week before the final DATALOCK. We replace the CPM with a CTRx Strategic Client Advocate (SCA).  

Project Management Rescues

Project Management Rescues

Project Management Rescues

 CTRx allows Study Sponsors to take back the CONTROL, VISIBILITY, COMMUNICATION, and QUALITY.  Our Strategic Client Advocate (SCA) will hold CROs ACCOUNTABLE to exceed expectations daily by operating Clinical Trials/RWE-RWD studies at FULL POTENTIAL, at MAXIMUM SPEED, and at the HIGHEST EFFICIENCY.

Strategy & Budget Rescues

Project Management Rescues

Strategy & Budget Rescues

Our Strategic Client Advocate (SCA)  foresees CRO Science and Operational Strategy failures and can rapidly deploy our Strategic Process Excellence model to REMOVE DELAYS and INCREASE BUDGET COMPLIANCE. Our Executive  Leadership, CTRX SCA's, and Budget Performance Audit teams hold CROs responsible for Operational Excellence and accurate Units Billed vs. Worked Completed from Day 1. 

patients deserve better than CRO Failures

Strategic Delivery Excellence

Interim & Final DataLocks delivered in over 300 Global Protocols and 900 Projects

  • 38 DAYS ahead of schedule  
  • INCREASED the number of trials within budget by 97%
  • REDUCED the number of SOW/UAT set-up errors by 98%
  • DECREASED the number of client issues by 94%
  • INCREASED Voice of the Client (VOC) client approval ratings by 78%

FSP-Service Value Added Model (SVAM)

When using CROs, CTRX provides the Pharmaceutical, Biotech, and Medical Device industries the flexibility to take back the clinical trial study

  • Control
  • Visibility 
  • Communication
  • Quality 

BAP-BEP-Service Management Delivery Excellence

Business Acquisition Process (BAP) & Business Execution Process (BEP) Alignment

  • Superior Science-Operational Strategy Excellence
  • Integrated Stakeholder Relationship Collaboration 
  • White Glove Budget and DATALOCK Delivery Accountability 
  • Metrics Milestone Management
  • Organizational Optimization 
  • Key Resource Retention 

Pricing Tool Validation, Units Billed, and Budget Audits/Solutions

Project Examples to Increase Profitability & CRO Financial Accountability  

  • CRO Units Billed to Sponsor vs Actual Work Completed by CRO Audit
  • SAE Reconciliation Completed by CRO vs Units Billed to Sponsor Audit
  • New Pricing Tool for Patient Recruitment Firm
  • New Pricing Opportunities/Functionality and Current Pricing Validation 
  • Pricing Tool and Development Standardized Proposal Template
  • Development of Global, Domestic, and Regional Pricing Tool Models 

Clinical & RWE Study Strategic Excellence Rescues

Deploy Center of Excellence (COE) and SET (Study Execution Team) models

  • Lead global Clinical Operations and Real-World Evidence (RWE) science, strategic, and operational advisory SET committees to support Clinical Trials (phase I-III), Late Phase, and RWE generation projects for the medical and development functions for Study Science Leads (Epidemiologist), Global Medical Strategy Leads, Operation Leads, Medical Affairs, HEOR, Medical Writing, Biometrics, Clinical Development, Clinical Operations, Privacy, Legal, Compliance, Safety, Regulatory, Data Management, Outsourcing, and Medical Communications, Clinical Pharmacology & Exploratory Development, and Pharmacovigilance. 

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Clinical TrialRx

2 East Main Street, Pittsboro, IN 46167, United States

+1(317) 892-9290

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