Joe Dustin Email & Phone Number

New Jersey, United States

Needham, Massachusetts, US

Working closely with our product, commercial teams and our clients to to articulate product vision, quantify value drivers, commit to the roadmap, form key partnerships and service our addressable market. BioFourmis is a leading enterprise platform and technology enabled service for digital biomarker development in clinical trials.

In January 2024, I started a life sciences technology advisory and consulting firm specializing in software and services for Clinical Development. The goal is to work on a fractional basis with pharma and biotech companies on technology strategies as well as eClinical software and services vendors and CROs on Go to Market strategies, product development.

Washington, DC, US

Chairman of the RAC for the Americas region. We are a diverse set of experts from all corners of the drug development industry. We advise executive management and the Board of Directors of DIA on changing trends and national issues that should be considered.

Washington, DC, US

As Vice Chair of this advisory board, we analyze industry trends in North and South America to advise executive leadership and the board of directors of DIA on what they should be considering for the coming year for annual planning purposes. We also contribute to the annual meeting and innovate on ideas with it's membership.

Washington, DC, US

I am a member of the DIA's Regional Advisory Council for the Americas. My role is to represent how technology, both in and outside the life sciences industry, can impact the agenda of DIA overall.

Palo Alto, CA, US

Leading the eCOA business at Medable as the link between Product, Delivery, Sales and our clients.Changing the way eCOA is delivered to the market by employing new business models through a platform for Decentralized Clinical Trials.

Palo Alto, CA, US

Building the future for Decentralized Trials, today.

Conshohocken, Pennsylvania, US

In addition to my work at BMS, I am also Co-leading the initiative for adoption of eSource data capture in Clinical Trials. Work with various industry stakeholders in Pharma and Regulatory to optimize the global use of electronic data sources and influence more efficient data gathering practices to benefit patients, clinical sites, and trial sponsors.

Lawrence Township, NJ, US

In this role, I led the strategy for new business capabilities within Global Development Operations that would allow BMS to conduct clinical trials better, faster and safer. My role was responsible for Clinical Trial Innovation and Change Management as a capability to ensure any new idea or process that is tested successfully gets implemented at scale.

New York, NY, US

In this role, I assumed shared responsibility for our Top CRO Partner clients around the Patient Cloud - which morphed into the Decentralized Clinical Trial (DCT) offering of Medidata as part of the whole Clinical Cloud platform. I was responsible for bringing together industry expertise, technology, strategy and creative solutions to successfully move.

New York, NY, US

After spending time in the Product Development Organization, the mobile health solution became more mature as we took careful time to build it out to customer needs and achieve product market fit. For 2.5 years I helped grow the Patient Cloud business exceeding targets by 200% and signing our first key enterprise deals for eCOA Transformation at Large.

New York, NY, US

In this product focused role, I was a key member of the goto market team on what became "The Patient Cloud" - Medidata's patient facing technology for clinical trials. This (at the time) was a new take on electronic patient reported outcomes (ePRO) which embedded wearables, digital endpoints and emerging mobile health methodologies into the solution to.

New York, NY, US

As a senior member of the Solution Consulting team I led over 1000 customer facing product demos and value presentations. My role was to regularly engage with clients and partners as well as our internal product teams to develop and sell solutions to life sciences organizations. I contributed to the strategic alignment of the Medidata Clinical Cloud.

etrials was acquired by Merge Healthcare in 2009, and then acquired by IBM Watson Healthcare in 2015, which was then spun off as Merative in 2022.I was hired as an Associate Project Manager, and promoted to full Project Manager in 6 months. I managed a team of developers and testers to complete projects on time and on budget. My job was to spec, design.

In 2019 CRF Health merged with Bracket and became Signant Health.Responsible for the implementation of customized electronic patient diary solutions for our clients in the pharma industry. I created extensive project documentation, end user training material in accordance with our Quality Management System, as well as managed customer expectations, project.

LogisticsBuilt and developed best practices to deliver finished products to our customers. (Palm Pilot eDiaries loaded with our custom software) I managed deployments for over 15 different clinical trials in North America and Europe whilst in this role. General tasks included IT support, hardware troubleshooting, hardware procurement, application support.

I joined CRF Box (Now CRF Health) in the early startup days of the US operations when there were about 7 employees in the US office, and about 60+ in Europe. I managed the internal IT infrastructure of the US office located in Cambridge MA. The backend system was linux based using SendMail, Tomcat/Apache, SSH, and other types of open source applications to.

Bs, Computer Information Systems

Digital Health Strategy

Education record