Your nimble & experienced clinical operations team

By closely aligning our methodology with your team’s needs, PharPoint’s clinical operations team provides flexible, tailored plans that meet your study requirements and ensures timely communication and goal completion.

Why choose PharPoint Research?

Our fully integrated, multi-disciplinary team is tailored to meet the needs of your study, equipped with consistent communication and a full knowledge of study direction. We have a field-based and in-house clinical research associate (CRA) team structure, allowing us to communicate study needs and remedy obstacles as they arise.

We provide special attention and strategic planning to optimize enrollment, and proactively manage obstacles such as subject screen challenges and excessive dropouts. PharPoint provides both internal and site team training on the protocol, study implementation guidelines, and issue escalation processes to mitigate enrollment risks.

Our team identifies sites that meet enrollment expectations while focusing on subject retention. In addition to site feasibility and qualification audits, PharPoint’s industry network allows us to connect sponsors with sites we’ve had positive working relationships with in past studies.

Our comprehensive services include:

Global clinical trial project management
Clinical monitoring
Site feasibility assessments
Investigator meeting preparation and presentations
Risk mitigation
Study startup support
Site management and communication production
Vendor management
Interactive Voice Response System (IVRS) vendor selection and oversight
Clinical Trials Management System (CTMS)
Investigator grant and research budget preparation and administration
Study rescues


Virtual trial capabilities →

Full-service capabilities →