ABOUT US
PharPoint Research is a US-based, privately owned contract research organization (CRO) that provides nimble drug development solutions to clients of all sizes.
Founded in 2007 by three long-time colleagues, PharPoint offers a range of clinical trial services and solutions (including clinical operations, project management, biostatistics, and clinical data management) to clients of all sizes across a wide range of therapeutic areas and clinical trial phases.
At PharPoint, we put our clients and the patients whose lives they impact at the core of everything we do.
WHY CHOOSE PHARPOINT?
What makes the PharPoint team different?
CLIENT-FOCUSED APPROACH
PharPoint’s client-focused, personalized and attentive approach ensures our clients (regardless of size) are able to meet their study goals. Our team is agile and scalable to meet our clients evolving needs.
COLLABORATIVE TEAM
PharPoint provides clients with a team that is attentive, experienced, and collaborative. From the start, our teams work closely with cross-functional groups to ensure high quality deliverables are produced according to industry-best timelines.
FASTER TIMELINES
Thanks in part due to our nimble size and experienced teammates, PharPoint is able to provide clients with faster study timelines — because patients are waiting.
EXPLORE RELATED RESOURCES
Clinical Trial Activity in Japan and Taiwan (2015-2025): Trends and Phase Distribution
A look at a decade of Phase 1-4 studies in Japan and Taiwan, from 2015 to 2025 according to ClinicalTrial.Gov.
Research is Personal | Video
Clinical trials are both scientific and deeply personal. This short video reflects the perspective that guides our work in supporting sponsors and patients.
Preparing for ICH E6(R3): Understanding the 11 Core GCP Principles
Explore the 11 GCP principles outlined in ICH E6(R3).
Exploring Multiple Perspectives in Rare Disease Trials
What makes rare disease trials unique? Explore perspectives across functions from a rare disease CRO team.
Database Build: Our Standard Timeline from Final Protocol to Database Go-Live
How long does it take to go from final protocol to database go-live?
Examining Strategies for Faster Clinical Study Report Timelines
Examining Strategies for Faster Clinical Study Report Timelines How long does it take a medical writer to produce a high-quality clinical study report (CSR)? What can a medical writer do to help speed up this turnaround without sacrificing quality? Biopharma companies are under increased pressure to reduce timelines, yet this
RECENT INDUSTRY RECOGNITIONS
2024, 2023 Triangle Business Journal Best Place to Work
PharPoint was proud to have been named to the Triangle Business Journal’s “Best Places to Work” List in 2023 and again in 2024! The Best Places to Work Awards are an annual program that recognize outstanding companies for positive work environments and policies that employees value. Winners are chosen based on employee survey feedback, conducted annually by The Triangle Business Journal.
2020 Triangle Business Journal Life Sciences Award: “Most Innovative CRO”
PharPoint is proud to have received the “Most Innovative CRO” award by the Triangle Business Journal! Based in the Research Triangle region of North Carolina, a nexus of the CRO industry, the business journal holds its Life Sciences Awards each year to recognize individuals and research organizations that are leading the field.
2019 Scrip Awards “Best Specialist CRO” Finalist
PharPoint is incredibly proud to have been selected as a finalist in the 2019 Scrip Awards “Best Specialist CRO” category alongside some of our innovative industry peers. The Scrip Awards are voted on by judges who are senior executives from biopharma and investment firms along with clinical research leaders.