Solutions

Strategic Resourcing

Engagement-based Solutions Designed to Limit Risk and Accelerate 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.

Satisfying Your Needs for Greater Flexibility, Control and Speed

Well-vetted hard-to-find resource pipelines

Flexible, configurable operating framework

Infusion of targeted assets to accelerate projects

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.

Biostats/Programming & Data Mgmt

Regulatory Consulting

Clinical Operations

Experience - Senior, Mid, Entry-level
Discipline - Biometrics, Regulatory, Clinical Operations, Medical Writing, Pharmacovigilance
Proficiency - Technical/platform expertise

Timeline - Length of deployment
Engagement - Projector milestone based
Scheduling - Weekly requirement thresholds

Veristat-managed
Client-managed
Hybrid management
Governance and oversight protocols
KPI reporting and dashboard

Veristat systems/SOPs
Client systems/SOPs
Hybrid approach

Common Sponsor Challenges:

Sourcing hard-to-find expert 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

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

Learn how we provide you with the right resources when you need them.

Contact Us Today!

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Strategic Resourcing

Engagement-based Solutions Designed to Limit Risk and Accelerate Milestones

Dedicated Resources that Seamlessly Integrate into Dynamic Clinical Environments

Satisfying Your Needs for Greater Flexibility, Control and Speed