Clinical Operations

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.

PharPoint’s clinical leadership team averages 20+ years of industry experience.
We design project teams as an extension of the sponsor’s team, establishing an environment that facilitates engagement and collaboration. Starting at kick-off, we begin building essential team dynamics and communication strategies.


We recognize that every client and study is different.
Our team & study approach is tailored to client needs. We offer flexibility in process to tailor team structure, and typically structure a study team to provide both a primary point of contact (project manager) and primary contact for each functional service.


Quality and client satisfaction are our key business objectives.
We work hand-in-hand with sponsors to offer consultative, client-focused guidance, and truly believe that client satisfaction is more important than utilization.

Our comprehensive clinical operations services include:

Global clinical trial project management
Clinical monitoring
Traditional, virtual, and hybrid capabilities
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

Decentralized study capabilities

PharPoint’s clinical operations team offers traditional as well as remote, virtual, and hybrid study solutions.

By partnering with leading virtual trial technology providers, we provide clients with access to all the tools necessary for a smooth decentralized study experience.


Virtual trial capabilities →

Full-service capabilities →