CRO-Centered Services

CRO-Centered Clinical Trial Services

Our goal is simple – to help you win and retain business. Imperial has undertaken a decades-long journey to become the only provider in the clinical research space that delivers customized support and a full suite of unique services designed for CROs.

 

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Advantages Gained Working With Imperial

  • A Single Point of Contact
  • Competitive Pricing
  • Budget Estimates in 2 Business Days
  • Bid Defense Support
  • Expedited Service Requests
  • Protocol-Specific Solutions
  • Evidence-based Strategies
  • International Considerations and Global Logistics Expertise
  • Governance: Working Group Meetings, Internal Client Health, Key Performance Indicators
  • Avoidance of Challenges/Pitfalls in Clinical Study Planning and Execution

See Case Studies, Creative, and other Work Examples here

Your Backroom Resource

Time is golden. The clock is always ticking, and Imperial can free up hours and days for you. We give you a competitive advantage and add significantly to your portfolio of services by becoming your backroom resource. We step in wherever you need us, work side by side with you, and can remain seamlessly behind the scenes.

Process, Discipline, and Execution

We get the job done. Our work is fueled by best practices for global project management, and our engaged project managers (not order-takers) are dedicated to the success of your clinical studies and have a track record of success.

Meet Your Study Goals Without the Hassle

Bridge a full set of study management gaps or get bolt-on-specific services from our subject matter experts.

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Study and Site Print Materials

Site tools and materials for study management, data collection, and patient engagement have long been an Imperial specialty. With the creative team and the printing operation at a single company, you will experience streamlined precision unavailable elsewhere. And we are experts at crossing the finish line: We create, print, fulfill, and distribute more than 50,000 shipments annually into over 100 countries for our clients.

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Clinical Trial Translation Management

Accuracy counts when it comes to translations, and that's why our team of translators is vetted, in-country, and has clinical experience. Imperial offers high-quality translations into more than 100 languages and dialects. 

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Ancillary Trial Supplies and Equipment

Our services go far beyond procurement, offering everything from managing expiry to technology programming. We have years of expertise in getting supplies and equipment to their international destinations and working through bureaucratic red tape.

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Clinical Trial Patient Engagement

Imperial gives you evidence-based global support services for subject recruitment and retention based on decades of experience. Our award-winning creative services, messaging, and solutions are proven to drive clinical study interest and obtain results in the patient, caregiver, and medical communities.

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Questions We Hear Most Often

A: It reduces complexity, speeds execution, and minimizes risk by eliminating handoffs between separate teams. When writing, translation, design, production, and logistics operate within one coordinated workflow, materials move faster, communication is clearer, and study teams avoid the delays that come from managing multiple timelines and priorities.

A: No. It supports your team by removing time‑consuming coordination work. Your internal experts stay focused on strategy, oversight, and decision-making while we handle the operational details, including version control, production schedules, translation workflows, and logistics. Everything stays aligned without adding to your workload.

A: Yes. You can engage one service or a full integrated workflow depending on your needs. Some teams start with a single service, such as translation or ancillary supplies and equipment, and expand as they see the benefits of centralized coordination, shared context, and smoother cross-functional movement.

A: Fewer handoffs and fewer vendors mean fewer delays. When writing, design, translation, and production operate within one workflow, files move quickly from creation to approval to site readiness. This reduces rework, shortens review cycles, and helps studies stay on schedule even when protocols evolve.