Deep Understanding Across Multiple Disciplines

We are focused on serving the biopharma/biotech market and strive to be a consultative and proactive oncology CRO partner.  Our customized solutions are designed around the individual needs of each of our biopharma clients.

Our people, company culture and can-do attitude, along with our unique combination of oncology and rare disease expertise and technology, differentiate us from our competition.

We seek to be more than simply a vendor, by adding value to the clinical development of our biopharma client’s emergent therapies. We pride ourselves on our commitment to delivering high-quality service.

Our Oncology Proposition:

  • Scientific and operational expertise in complex trial designs, i.e., adaptive, basket, umbrella
  • A team with 100% oncology experience
  • Dedicated teams to early and later phase trials
  • Understanding the risks and contingencies to delivering any project on time
  • Technology enabled
  • Proactive partnership approach
  • Close communication between our team, sites and sponsor


Our Work In Complex Trial Designs

We excel in delivering trials evaluating the latest advances in investigational therapies.  Our team is well versed in a plethora of trial designs including dose escalation both biomarker based and not, blind/double blind, cross over trials and others.  Our experience enables our ability to help sponsors develop or deliver a personalized approach to medicine and an increased efficiency in investigational product development.

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Why work with us?

Helping you succeed in your project


Oncology Studies Delivered


Investigative Sites Globally


Oncology Patients Involved

15 Years

Industry Experience for all our Project Leaders


Team Oncology Experience


Examples of Our Complex Trial Design Experience

Interaction designs

Defined as enrollment of marker + and – patients with randomized to targeted vs. non-targeted therapy

Enrichment designs

Defined as enrollment of marker + patients only, with or without randomization

Adaptive enrichment designs

Defined as adaptable enrollment during trial from full population to patients who seem to benefit from product under study

Marker strategy designs

Defined as patients randomize to treatment strategy: based on biomarker status vs. not based on biomarker status (e.g., physician’s choice)

Master protocols

Basket trials, umbrella trials, platform trials, etc


Supporting Case Studies

MANY MANY thanks for your ongoing support. You have all been top notch, and we are so thankful to be working with Cmed on this study.

Your willingness to work through the problem and find a solution shows the site we’re working hard to provide them with the best possible solutions. This is great news and makes me feel really good about selecting Cmed as our vendor.

How quickly Cmed collectively got the study up and running with our first SIV and FPI likely to be ahead of the planned date. It has ‘mesmerized the investors’.

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Let’s support you on your next project