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Functional Service Provider for Innovative Healthcare Solutions

Clinical trials need customizable clinical research support that leverages broad functional service and therapeutic area expertise. Catalyst Flex is a multi-therapeutic functional solution expert ready to support your clinical research needs.

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An experienced functional service provider for clinical trials

Catalyst Flex uses a flexible, scalable, and agile FSP model to reinforce a client’s global clinical trial activities.  We design solutions that bring forward flexible and innovative scientific approaches. Catalyst Flex delivers. We support you whether you need a couple of staff or an entire team.

Solutions and dedicated teams to serve research development 

Catalyst Flex offers support across multiple therapeutic areas to help drive collaboration for a study to succeed. We start with listening to and learning about your specific needs and then customize the people, processes, and/or technology, collaborating and committing to meeting your needs. With access to an extensive network of staff across the globe, we deliver a global or local solution.

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Broad spectrum of global, strategic experience

Catalyst Flex clinical solutions and offerings help to achieve high-quality, cost-effective results. We are committed to operational excellence. We have successfully delivered for more than 180 clients on over 900 trials across functional areas. Experts lead client projects in the functional areas of clinical operations, data management, biostatistics and programming, safety, and medical writing.

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Catalyst Flex properly identified the resource we needed, aligned with our very short turnaround timing, and was available to support us.

Catalyst Flex has been instrumental in streamlining our clinical research programs. Their expertise and dedication have significantly improved our efficiency and outcomes.

Personalized clinical research services to enable your programs 

Catalyst Flex individuals and teams are dedicated to succeeding across multiple therapeutic area studies with customizable solutions.

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Success Stories
Phase III rare disease rescue

A small biotech with limited internal capacity outsourced a Phase III clinical program in patients with a rare, life-threatening necrotizing soft-tissue infection for which no therapy currently exists. The study was to be conducted with 60 U.S. sites with the objective of enrolling 290 patients.

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Flexible data management for a growing portfolio of studies 

A small biopharma client with a large pipeline of 25 to 30 studies across Phase I and II studies needed to enhance their in-house biometrics capabilities using additional data management service support.

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