Strategic Resourcing

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Whether you need a few scientific experts or a fully-staffed function, gain flexibility and results with Veristat’s Strategic Resourcing Solution and confidently meet your study milestones.

Clinical study leaders in small and mid-sized biotech organizations in particular work with Veristat to address their limited capacity challenges across all functions of novel drug development. We supply hard-to-find and highly skilled scientific resources that seamlessly integrate into your in-house processes and environments and satisfy your needs for flexibility, control and speed.

Prioritizing quality over quantity, Veristat consistently delivers greater levels of customer value and satisfaction. Specialized, demand-driven resourcing from Veristat ensures your focus remains where it should be: meeting study milestones and accelerating time to market.

Dedicated Resources that Seamlessly Integrate into Dynamic Clinical Environments

Backed by the strength of a world-class CRO with 27 years' experience in clinical trial planning and execution for novel therapies, our scientific experts are ready to solve your talent acquisition challenges. A pipeline of discipline-specific expertise tailored to your requirements, built-to-order integration, and deployment of a modular construct of processes and oversight transform your once time- and risk-intensive pursuits into a highly efficient and rapidly scalable resource supply chain.

Manage Your Resources Exactly When and Where You Need

We set fresh expectations for what it means to be science-centric, beginning with a comprehensive understanding of your needs. Whether your requirements center on biometrics and data management, regulatory consulting, clinical operations or medical writing— or all of the above— benefit from our experts to rapidly fill your skills gap and augment your team so you keep even the most complex activities advancing at full speed.

Common Sponsor Challenges:

  • Sourcing hard-to-find experts in clinical operations for novel therapies 
  • Integrating a team to support patient accrual rates while maintaining data submission timelines 
  • Securing Regulatory Affairs lead to take Sponsor through to NDA submission 
  • Progressing a stalled trial 
  • Deploying medical writers on a rolling basis 
  • Reducing activation times for clinical trial sites 
  • Accelerating a database build 

Veristat Results Delivered:

  • Capacity gaps filled with fully-vetted expert resources 
  • Business-as-usual for mission-critical work 
  • Dedicated on-site skill set  
  • Scale-up/scale down flexibility 
  • Compliant, rigorous, repeatable processes 
  • Hard-to-find experts in medical writing, statistical analysis, clinical trial reporting
  • Clear study planning 

Learn more about Veristat's services here.