Clinical Trial Services

Efficiently and strategically plan, execute, and analyze Phase 1 – Phase 4 clinical trials with support from our experts.

PharPoint was founded in 2007 with a rebellious spirit and a firmly focused mission: to create an alternative to rigid, unimaginative, quality-compromised clinical research organizations. We’re proud to have supported innovative clients for 1,000+ clinical trials over the past 15 years, including 30+ successful regulatory submissions.

Our services include:

Site Feasibility & Study Start-Up

Don’t waste resources by activating low- or non-enrolling sites. PharPoint combines extensive data mining with an experienced team to help Sponsors make informed, objective decisions on which sites to select for a faster, more effective clinical trial.

Clinical Operations

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

Our 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 Management

PharPoint’s highly experienced clinical data management team prioritizes your data, working proactively and cross-functionally to expedite timelines after last patient, last visit.

DMC Support

PharPoint has extensive experience supporting and managing Data Monitoring Committees (DMC), also known as Data and Safety Monitoring Boards (DSMB), Data Safety Monitoring Committees (DSMC), or Independent Data Monitoring Committees (IDMC).


From start to finish, PharPoint guarantees high-quality statistical analysis and reporting services and can assist with any combination of services needed at the clinical development stage.

Medical Writing

Get clear and concise documents with PharPoint’s medical writing services.

Study Rescue

Working with a CRO that’s falling behind or failing to deliver results?


Hear what our clients and partners have to say

“There is an inherent honesty and authenticity in [PharPoint’s] approach. …I have complete faith and trust in PharPoint as our partner, and that gives me confidence in the success of our clinical program.”

Client, Pharmaceutical Company

“I can highly recommend partnering with PharPoint.  Not only were documents provided to our site in a timely manner, communication with all parties from the CRA to the project managers has been excellent.”

Partner, Study Coordinator

“…High priority pivotal studies locked and delivered faster than any other CRO I have worked with in my experience. Not only was the study delivered within budget and early, it was a quality deliverable.”

Client, Biotechnology Company