Explore our Services & Capabilities

PharPoint Research is a client-focused contract research organization (CRO) that can provide clinical trial support to sponsors navigating pre-IND through phase 4/post-approval.

How can PharPoint help me meet my clinical trial goals?

Clinical Trial Consulting

Confidently make informed decisions and advance your product along the development pathway with support from our regulatory, clinical, medical, and biometrics consultants.

Site Feasibility & Study Start-Up Services

Use PharPoint’s objective analysis and insight to identify, activate, and partner with high-performing sites that can help you meet study enrollment goals.

Clinical Data Management Services

Partner with a proactive data management team that prioritizes your trial from day one – allowing for a rapid database lock only five days after last patient last visit and final source data verification.

Biostatistics and Statistical Programming Services

Our consultative approach to our biostatistics services includes a level of responsiveness, support, and proactiveness that’s unmatched within the industry. (And did you know? 100% of PharPoint statisticians have advanced degrees.)

Clinical Operations and Project Management Services

PharPoint’s team of clinical research associates (CRAs), clinical operations leads (COLs), project managers (PMs), and other clinical staff are experienced and dedicated to timely, thorough support for your study sites.

Medical Monitoring Services

PharPoint’s study physicians work collaboratively as integrated members of your team, supporting project teams, sites, and Sponsors with information to facilitate discussion and decision-making for the medical aspects of a study.

Data Monitoring Committee (DMC) Services

Will your study have a data monitoring committee? Bring along an independent partner to set your DMC up for success, support DMC members, and manage logistical challenges.

Medical Writing Services

Receive clear and concise study-related documents with support from PharPoint’s medical writing team.

Clinical Trial Rescue & CRO Oversight Services

Regain clinical trial transparency, boost data cleanliness, and get your study back on track through the use of varied levels of support from the PharPoint team.

Tailored support to help you meet ambitious clinical trial goals

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