Why do sponsors choose PharPoint?
180+ clients 1,000+ trials
A team without silos
Effective trials require early input from every angle. PharPoint brings together cross-functional teams early and often, aligning priorities and anticipating challenges.
Attentive & experienced
PharPoint’s proposed team leads are experienced in the areas that matter most for your individual trial, with the ability to prioritize your study from day one.
Faster study results
PharPoint’s repeatable biometrics timelines provide clients with rapid study results thanks to early planning, proactive processes, and an attentive team.
Sounds great. But I have some questions…
We’re looking for a CRO that can provide us with strategic guidance.
PharPoint was founded from consultative roots and believes in a transparent, strategic approach with a client’s best interests in mind. We regularly work hand in hand with sponsors to share lessons learned and discuss ways to efficiently move their programs forward.
I’m looking for a CRO with very specific experience. Does your team have….
PharPoint teammates have experience from Phase 1 through Phase 4 trials involving a wide variety of therapeutic areas and special populations. We are always open to discussions regarding our team’s specific experience as it relates to your upcoming trial.
We need a CRO that can scale up to support future trials. Is PharPoint large enough to support this?
Yes! PharPoint has experience supporting large development programs that have multiple studies running concurrently. For clients with multiple studies, PharPoint prioritizes program-wide efficiencies and shared client and program knowledge, managed by an assigned program lead.
How does PharPoint compare to the leading top 10 CROs?
Top 10 CROs
Attention & study prioritization
You want support from a CRO that prioritizes your trial from day one, including strategically planning ahead and always keeping you in-the-loop.
Study team experience & consistency
Outside of organizational experience, the team actually working on your study is equipped to handle potential challenges with minimal handoffs and long-term involvement.
Senior team involvement
You want direct communication with senior resources and support from a leadership team that’s invested in your success.
Transparent, accurate budgeting
You’re looking for a partner that works to bid accurately from the start, avoiding underbidding and costly scope changes later. You want true vendor passthrough costs with no added premiums.
CLIENT:
Small rare disease company
SERVICES PROVIDED:
Clinical operations, data management, biostatistics
“After a less than positive experience with a large CRO, we knew we needed a CRO who was vested in our collective success, a true and trusted partner who would be flexible, attentive and engaged in achieving our end goal. We also needed to work with an experienced, competent team who we could rely on and an approach to the contracting that offered value, without compromising quality. In our partnership with PharPoint we have found all of this and more.“
General Manager
CLIENT:
Global biotechnology company
SERVICES PROVIDED:
Data management, biostatistics
“The team members, the communications, the hard work and dedication of the PharPoint staff is all second to none. We work globally and the team has on occasion worked extremely hard outside of normal business hours to assure the study was taken care of and milestones were met. “
VP Clinical Operations
FAQs
PharPoint is a US-based, privately held CRO founded in 2007. We’ve grown organically over the past 15+ years by delivering reliable support that earns repeat business and strong client referrals. Our team has supported more than 1,000 studies and is happy to share case studies and testimonials.
PharPoint’s data managers and biostatisticians regularly support global clinical trials.
For global studies outsourcing study management and monitoring, PharPoint’s clinical operations team can work side-by-side with other organizations (whether it’s sponsor’s in-house team, a local CRO of the sponsors choice, or one of PharPoint’s non-US partners) as the designated US team.
PharPoint’s capabilities include clinical operations, project management, data management, biostatistics, medical writing, clinical trial consulting, and clinical trial rescue. We also maintain deep partnerships with specialty vendors outside our core areas of expertise. Explore our services.
The PharPoint team is fully US-based, with two North Carolina offices and remote employees across the country.