Greenphire is the leader in global clinical trial payment automation. Greenphire’s best-in-class solutions optimize clinical trial performance by streamlining payment workflows from sponsors and CROs to sites and participants. Greenphire’s ClinCard, eClinicalGPS and ConneX solutions easily handle any type of trial design and complexity, resulting in more accurate and compliant payments and travel globally for both sites and participants. The choice of industry leaders worldwide, Greenphire provides better performance and better data, resulting in better trials. Learn more at www.greenphire.com.


Greenphire's EnvisiX solution is a budget build and negotiation tool that enables sponsors and CROs to effectively and efficiently build a study budget. The tool provides a streamlined and controlled workflow for budget negotiation for sponsors and CROs with complete transparency and management of rates, adjustments, adjudications, approvals and more.

ConneX is a global travel solution providing in-market services and support, designed to meet the unique travel needs of each study, whether it be for rare disease, diverse populations, pediatrics, etc. Our offering removes the burden of complex travel arrangement from site staff, while peace of mind is established for participants, their families and caregivers.

With more than 7 million payments, ClinCard is the industry-leading method for automated participant payments, delivering unmatched simplicity, security, and global reach.

eClinicalGPS is designed to automate and streamline clinical site payments, getting sites paid faster and more accurately with less administrative burden. Configured


The site budgeting and contracting process is critical to the success of a clinical trial. Enhance your study design and startup with EnvisiX. Watch this short video to learn more.

ConneX interview with Jim and Kyle - Part 7 Jim summarizes the end goal of Greenphire's ConneX Expert Travel Solution - focusing on making the clinical trial experience as simple as possible for participants while reducing the administrative burdens on the site.

ConneX interview with Jim and Kyle - Part 4 Kyle talks about the importance of patient convenience (humanizing clinical research) - removing the barrier of participation in clinical trials.

Director of Clinical Research at MidLantic Urology, Cheryl Zinar, discusses how introducing rideshare has improved the clinical trial experience for all stakeholders – Added convenience and removed out-of-pocket costs for patients, simple workflow and improved control for study coordinators and increased enrollment and reduced costs for the site.

ConneX is the most comprehensive clinical trial travel solution designed to meet the unique needs of your global trials.  

Sponsors, CROs and sites around the world partner with Greenphire to enable a secure and compliant electronic payment technology that makes their lives easier and removes the barriers to successful recruitment and retention. Watch this video to see how it works!

Learn how Greenphire's eClinicalGPS site payment solution offers flexible delivery models to maximize ROI, adoption, and help sponsors and CROs meet their business objectives.

Learn how automating payments to research sites improves research site performance, supports site sustainability and delivers a more collaborative, trusting relationship between research stakeholders.

Gain an understanding around site payment burdens and how our solutions can empower sites around the world.

Learn the advantages that sponsors and CROs gain when choosing to automate site grant payments.



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Contact: Wayne Baker


  • New Greenphire Data Indicates Clinical Trial Industry’s Swift Rebound; Patient Enrollment Reaches Pre-Pandemic Levels

    Greenphire, the global leader in financial lifecycle management for clinical trials, says patient enrollment for global clinical trials has returned to pre-COVID levels. Research spotlights the need for technological solutions to help participants suffering through financial and logistical hardships to stay enrolled in studies.

  • Driving Clinical Trial Sustainability In The Time Of COVID-19

    With the current clinical trial logistical challenges there comes the need for ingenuity – partnering with a travel provider who can navigate these difficult and uncertain times to ensure sustainability for the trial.

  • How Sponsors Can Ovecome The Growing Challenges In Clinical Trial Budgeting And Negotiation

    This paper seeks to explore the most crucial obstacles to successful budget design and negotiation in light of the current complexity experienced across the clinical trial universe. It highlights how technology can streamline these traditionally manual, time-consuming workflows, increase transparency and predictability, and deliver more current, and accurate data for an optimized study start-up.

  • The Michael J. Fox Foundation For Parkinson’s Research Works With Service Provider To Remove Reimbursement And Travel Obstacles For Clinical Study Participants

    In 2010, MJFF launched a large-scale clinical study conducted at a network of clinical sites around the world focused on identifying and validating Parkinson’s disease biomarkers. The study realized it needed a new way to ensure that participants were remaining engaged throughout the long protocol and that the experience was as seamless as possible for both the volunteers and the site coordinators. They were able to source a solution to support patient-centricity, as well as study site efficiency.

  • The Ultimate Guide To Purchasing A Clinical Trial Study Participant Reimbursement System

    This guide focuses on important areas to evaluate when vetting a platform for clinical research participant reimbursement. These crucial elements will help ensure the system you select improves the participant experience without increasing the burden on site staff.

  • How To Lose A Site In 10 Ways

    In partnership with the Society for Clinical Research Sites, Greenphire has conducted a survey to hear directly from sites regarding Investigator Grant Payments. As such, we would like to share insights from the survey and suggestions for improving site satisfaction as it relates to invoicing and payment processes. Here is a list of 10 things sites say sponsors and/or CROs do that add stress to the relationship.

  • The Impact Of COVID-19 On Research Sites: Planning For The Road Back To Full Trial Operations

    COVID-19 has had a dramatic impact on US clinical care, including how sites have worked to maintain research operations throughout the pandemic. The financial and logistical challenges faced by our site partners have been substantial, here is a recap of the adaptations they’ve made to manage through the current environment.

  • Clinical Trial Budget Challenges & Opportunities

    Protocol complexities are becoming ever more complex, and with it, so has the clinical trial budgeting process. Plagued by multiple stakeholders using disconnected systems across the globe, delays and increased costs in study start up follow. Discover what sponsors need to consider in order to achieve first patient in as swiftly as possible.

  • Addressing Global Workflow Complexities For Clinical Trials

    There are challenges associated with conducting clinical trials in newer markets. Processes and regulations may differ by country/region, making standardization across a global study nearly impossible. The key to developing solutions that meet all clinical and administrative workflow requirements and regulations is to listen to those who live and breathe these processes.

  • COVID-19 And Clinical Trial Regulatory Guidelines

    Recently, both the FDA and EMA issued guidance with regards to the conduct of clinical trials during the COVID-19 pandemic. These latest regulatory guidelines permit sites, sponsors and CROs to adjust their study operations to meet changing conditions for ongoing trials, however there are conditions that must be met in order for new solutions to be considered. Here are six steps the industry can take to support the needs of patients and sites.

  • What to Look For When Selecting An Investigator Payment Solution

    Many times sponsors go with a site payment solution they thought would work - only to find out the "automation" is not so automatic - that customer support is outsourced, spreadsheets still need to be emailed back and forth and sites are still calling asking questions. Following is a list of things to consider when choosing to implement investigator payment technology to avoid this situation.

  • Clinical Trials & Travel Tribulations: Improving Access And Outcomes For Patients And Caregivers, Sites And Sponsors

    In this paper, we dive into the logistical and financial challenges which increasingly impact all clinical trial stakeholders - from patients and sites, to sponsors and contract research organizations (CROs). Yet with proper planning and the right partners on board, travel arrangements and reimbursement programs can make the trial and patient experience more comfortable and successful for everyone.

  • Rideshare: Taking Clinical Research By Storm

    The new age transportation method, Rideshare, is growing in popularity amongst everyday travelers, but has also been found to provide significant advantages for clinical trials. This blog outlines ten Benefits of utilizing Rideshare through an expert provider in clinical workflow optimization.

  • Why Now Is The Time To Evaluate New Clinical Trial Technology

    Whether your trial isn’t starting for six months or has already started, assessing new solutions and adopting best practices through automation can streamline your operations and improve patient retention.

  • Midlantic Urology Associates Introduces Added Convenience For Patients With Rideshare Program

    Midlantic Urology Associates had been employing a single driver for all participant pick-ups. This proved to be inefficient and unsustainable, so they began utilizing taxis. This alternative was costly and unreliable – there had to be a better way. ClinCard’s integration with Lyft has not only improved the experience for patients and study coordinators but has also helped with recruitment as new patients are enrolling in the study as a result of this added convenience.

  • Complementing ePRO + eCOA Platforms With Patient Micropayments

    Sadly, the average drop-out rate across clinical trials is 30%. Greenphire has increasingly seen clients focused on increasing completion rates of patient reported outcomes and bolstering compliance using ClinCard. ClinCard has built-in text reminders for upcoming onsite patient visits and the ability to trigger “micropayments” when select tasks are completed.

  • Medical University Finds Solution To Track Participant Remuneration

    Concern ensued across the Medical University of South Carolina (MUSC) research faculty and staff when they received notice that departments would need to somehow track and sum all their petty cash, Walmart and Target gift cards, VISA cards and checks issued through Accounts Payable (as there was no institutional research policy standardizing a single type of remuneration payment for clinical research participants). A fellow academic medical school recommended ClinCard by Greenphire which ended up being the perfect solution.

  • How A Top CRO Used ClinCard To Create A Personalized Patient Experience For A Non-interventional Psoriasis Study

    The CRO realized that they needed to introduce new ways to keep participants engaged and interested if they were going to successfully support this trial. The CRO identified ClinCard as the ideal software that could instantly get study participants their stipends, without adding a burden on the site staff.

  • Industry Leading Biotechnology Company Automates Clinical Payments Enterprise-Wide With eClinicalGPS

    A Sponsor was facing difficulties with tracking payment details, critical for financial transparency and requirement details. Read how eClinicalGPS played an integral role in their mission to modernize clinical investigator payment processes.

  • Mission: Control Site Payments

    For years, Greenphire has heard from investigative sites, Sponsors and CROs that the site payment process is much like the “wild wild west” — with little consistency, confidence or clarity for everyone involved.