2025 Sponsors & Exhibitors

Cytel is the largest provider of statistical software and advanced analytics for clinical trial design and execution. For over thirty years, Cytel’s scientific rigor and operational excellence have enabled biotech and pharmaceutical companies to navigate uncertainty, prove value and make confident, evidence- based decisions. Our experts deliver industry-leading software, data-driven analytics, real-world evidence and strategic consulting. Headquartered in Waltham, Massachusetts, Cytel has more than 1,400 employees across North America, Europe and Asia. For more information about Cytel, please visit www.cytel.com. 

Dr. Vince Clinical Research (DVCR) is a full-service contract research organization (CRO) specializing in early phase trials in both healthy normal volunteers and patient populations across a wide range of trial designs and therapeutic areas such as neuroscience, substance abuse, pain, cardiometabolic disorders, infectious diseases and many others. CRO services include project management, data management, biostatistics, statistical programming, PK/PD analysis, medical writing, monitoring as well as site feasibility and management for multi-site trials. Additionally, DVCR operates one of the most innovative and technologically advanced clinical pharmacology units in the world with over 90 beds for overnight confinement, a cGMP compliant pharmacy as well as luxurious amenities to support diverse study participant recruitment and retention. By leveraging technology and one of the country’s most experienced leadership teams in early clinical development, DVCR provides Smarter Faster Data® to their biopharmaceutical clients. For more information, please visit https://sponsors.drvince.com/

For more information, please visit https://www.klick.com/

One2Treat is a forward-thinking partner for biopharmaceutical companies, dedicated to delivering transformative insights in clinical trial design, analysis, and market access evaluations to support holistic treatment decisions.

Driven by a commitment to patient-centricity, One2Treat leverages modern statistical methodologies and advanced software solutions, ushering in a new era of personalized healthcare. For more information, please visit https://one2treat.com/

PhaseV is a technology company leveraging advanced causal inference and machine learning to innovate clinical trials. Our technology and methods enable us to optimize trial design by detecting hidden signals in existing clinical data and extracting actionable insights, as well as supporting advanced adaptive designs for more efficient, precise and successful clinical trials. For more information, please visit https://phasevtrials.com/

Scimega is a niche Canadian oncology CRO acting in Canada within the context of global cutting-edge oncology trials sponsored by U.S. mid-size and smaller biotechs. Skilled in collaborative vendor teaming, Scimega guarantees sponsors the quickest site start-up and highest patient recruitment rate, without sacrificing premium quality data.

With an optimal operations design robust enough to address an ever-changing clinical trial landscape, Scimega’s team of Lean Coached oncology experts go above-and-beyond to provide: Local, full-time, permanent hires for exceptional staff quality; An extensive network of Canadian Investigator Sites that frequently emerge among top enrollers, and are activated 50% faster than average for global studies; Optimal site engagement to maximize quality, timely data entry and query resolution; Robust and Lean Scimega methodology and processes are supported by current technology to keep every trial this CRO monitors on the Lean trajectory.

Learn more about the Canadian opportunity or explore an expansion with Scimega!

For more information, please visit:

www.scimega.com    https://scimega.com/blog/       info@scimega.com

Worldwide Clinical Trials (Worldwide) is a leading global contract research organization (CRO) that works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications, from discovery to reality. Our full-service clinical development capabilities include bioanalytical laboratory services and Phase I-IV clinical trials, as well as post-approval and real-world evidence studies – all powered by our talented and accessible team of clinicians, scientists, and researchers who bring their first-hand expertise to each clinical program.

At Worldwide, we understand that each customer and project are unique, so we take a collaborative and personalized approach to identify and meet specific needs and goals. Anchored in our company’s scientific heritage, we are therapeutically focused on cardiovascular, metabolic, neuroscience, oncology, and rare diseases. We apply this deep therapeutic knowledge to develop flexible plans and quickly solve problems in the rapidly evolving clinical development landscape.

Our team of 3,000+ professionals spans 60+ countries, and believes that through collaboration, and a culture that embraces diversity, equity, inclusion, and belonging (DEI&B), everyone plays an important role in making a world of difference for patients and their caregivers. We are united in cause with our customers to improve the lives of patients through new, innovative therapies.

For more information on Worldwide, visit www.Worldwide.com or connect with us on LinkedIn.

Delve Health is an innovative biotechnology solutions company dedicated to revolutionizing the way clinical trials and healthcare organizations leverage data for improved patient outcomes and operational efficiency. By harnessing the power of wearables, biosensors and AI and leveraging the real-world data (RWD) collected by remotely monitoring patients, Delve Health delivers quality analytics to researchers and healthcare professionals. We provide actionable insights to make informed decisions, drive transformative outcomes and enhance patient care—all while removing social determinants of health (SDOH) barriers. For more information, go to https://delvehealth.com/

Barrington James are an industry leading, global recruitment business that exclusively serves the Pharmaceutical, Biotechnology and Medical Device sectors. With offices all over the world and hundreds of specialists dedicated to sourcing exceptional talent, we have the capacity and capabilities to deliver world-class recruitment solutions to Life Science companies of all sizes. To learn more, please visit https://barringtonjames.com/

BioPoint is a US-based life sciences consulting organization that brings decades of industry knowledge and expertise to our clients. We offer flexible support whether it is a need for a single resource or our specialized FSP approach, BioPoint can support all facets of drug development. To learn more, please visit https://biopointinc.com/.

Capish develops unprecedented tools for visualization and exploration of data, offering customer-specific solutions tailored to meet the complex challenges of clinical research. For more information, please visit https://www.capish.com/

For more information, please visit https://www.danforthadvisors.com/

Faro Health is bringing clinical trials into the digital age by helping teams manage and balance the complexity of modern trial designs through a cloud native platform. The Faro platform enables study teams to design complex clinical trials using small modular building blocks and combines that with data driven insights to orchestrate and automate operationally complex trials. Faro brings balance, centricity and flexibility to protocol development through automation and integration to downstream systems and vendors, ensuring they are always up to date and correctly configured. As a result, clinical trials using Faro are operationally efficient which avoid delays due to ambiguity and generate data that can be trusted. For more information, visit farohealth.com.

Govig Life Sciences Division’s expertise spans all multiple segments of life sciences, including Biotech, Pharma, Medical Devices, Diagnostics, Digital Therapeutics, Wearables, Radiopharmaceuticals, and other emerging service and product sectors. Through our expertise and successful placement activity, we help build your organization by addressing your needs now and throughout its life cycle. Emerging and midsized clients repeatedly retain us when they face tight timelines, knowledge and network gaps, resource constraints, or challenges related to scope and reputation. We put our tenure, relationships, and expertise to work so you can meet your deadlines, keep your promises to patients and investors, and build a successful organization. Learn more at https://govig.com/industry/life-sciences/

Halloran Consulting Group, a ProductLifeGroup company, is a life science consulting firm that provides strategic regulatory, quality, clinical, and organizational support in the pharmaceutical, biotechnology, and medical device sectors in the United States. As trusted industry partners we offer expertise in operational excellence, fostering innovation across the life sciences ecosystem. For more information, please visit https://hallorancg.com/

Harbor Clinical is a women-owned clinical research services firm. As a Functional Service Provider (FSP) offering Staff Augmentation, Consulting, and Single-Service resourcing models, Harbor Clinical’s mission is based on the goal of forging innovative partnerships, with sponsors and employees, built on a bedrock of communication and transparency. To learn more, please visit https://www.harborclinical.com/

ICON Biotech is a world leading healthcare intelligence and clinical research organisation, dedicated to the needs of small and mid-sized biopharma companies. With 8,000 dedicated staff, we help biotech organisations meet their critical milestones and deliver data and evidence-based results to investors, large pharma partners and regulatory authorities. For more information, please visit https://www.iconplc.com/sectors/biotech

Lumanity is a global healthcare advisory firm committed to bringing human perspectives to the forefront, integrated with sound science and business strategy, to realize a bold vision of fearless innovation and drive more authentic human touchpoints from discovery to care. Our passionate, diverse specialist team of patient advocates, clinical, scientific, and subject matter experts embed humanity and insight into meaningful solutions, co-created with communities to illuminate the path to healthcare that matters to patients. We believe the path of innovation starts and ends with the human lived experience. Learn more at https://lumanity.com/patient-engagement/

Miracle accelerates clinical trials with real-time, automated insights across enrollment, patient profiles, safety, labs, data management, forecasting, and more. By aggregating and harmonizing siloed data, Miracle helps biopharma companies reduce delays, make faster decisions, and centralize communication. Customers have cut months off trial timelines by eliminating manual processes and inefficiencies. For more information, please visit https://www.miracleml.com/

Novotech is a globally recognized full-service clinical research organization (CRO) and scientific advisory partner for biotech and small- to mid-sized pharmaceutical companies seeking to advance drug development. With deep therapeutic and regulatory expertise and an expansive global footprint across the Asia-Pacific region, North America, and Europe, Novotech offers clients an accelerated path to bring life-changing therapies to market. For more information, please visit https://novotech-cro.com/ 

Phesi’s patient-centric data analytics solutions can help you deliver smarter trials and faster cures. Our Trial Accelerator™ platform, powered by the world’s largest trials database, can simulate clinical trials and generate Digital Patient Profiles and Digital Twins, inform your program and protocol design, and improve country and investigator site performance. For more information, visit: https://www.phesi.com/

The PPD clinical research business of Thermo Fisher Scientific enable customers to accelerate innovation and increase drug development productivity. Utilizing patient-centered strategies and data analytics, our capabilities cover multiple therapeutic areas and include early development, all phases of clinical development, peri- and post-approval, novel approaches to patient recruitment and investigator sites, and comprehensive laboratory services. For more information, please visit https://www.thermofisher.com/ppd

Precision for Medicine is the first global, precision-medicine, clinical research organization and a leader in complex clinical development. Our clients benefit from advanced technologies and new approaches that compress timelines, gain efficiencies and increase the probability of approval. Under one global roof, Precision has worldwide CRO services, integrated sophisticated biomarker capabilities, technical manufacturing solutions and more. With 7 specialty labs and 3500+ professionals worldwide, we help clients accelerate life-changing treatments and propel medicine forward. For more information, visit https://www.precisionformedicine.com/

Rho, a global CRO headquartered in North Carolina’s Research Triangle Park, delivers comprehensive drug development services, from strategy to clinical trials and marketing applications. With more than 40 years’ experience, Rho partners with leading pharmaceutical, biotech, and government organizations, fostering collaboration to accelerate timelines, optimize ROI, and enhance program efficiency. For more information, please visit https://www.rhoworld.com/

Rivia is an integrated trial monitoring platform with AI-driven analytics, designed for clinical teams and medical leadership. It unifies data across vendors in days, enabling earlier interpretation and effective action on trial data. Sponsors like Alentis and Altrubio monitor patients and generate reports in minutes, unlocking the full potential of their therapies. For more information, please visit rivia.com

Signant is the evidence generation company that digitally enables trials—wherever and however you run them. Our SmartSignals ecosystem simplifies data collection, making the patient journey intuitive and the data journey seamless. Delivering proof at the speed of life, we help you advance therapies with confidence. When it matters most, count on Signant. For more information, please visit https://signanthealth.com/

Sitero is a next-generation clinical research partner, working with more than 200 Pharmaceutical, Biotech, and Institutional Research Organizations globally. Our innovative technology-driven approach enhances safety, compliance, quality, and efficiency in research and clinical trials, so customers can bring life-changing treatments to market safer and faster. Backed by a team of industry leaders in Technology, Clinical Operations, Biosafety, Drug Safety, Ethical Review/IRB, and more, Sitero combines the expertise of a tenured team with a nimble, innovative approach to clinical research. Sitero has offices in the U.S., U.K., and India. Learn more at sitero.com and on LinkedIn: linkedin.com/company/siterollc.

At SSI Strategy, we're strategic partners deeply invested in our clients' success. We offer a unique, adaptive approach to supporting biotech companies, integrating business acumen with deep expertise in Clinical Development & Operations, Regulatory affairs, Pharmacovigilance, Medical Affairs, Quality and more.

Our agile skills and resources model allows us to adapt to your specific needs, working as an embedded team within your organization. We complement your existing teams, scaling specialized skill sets up and down as needed, while equipping them with the tools and resources to operate at peak performance. By fostering the organization you want to build, we position your full-time employees to be more successful and effective in their strengths. As your needs evolve, so does our support. We offer deep expertise, strategic insight, and a comprehensive range of services to help you navigate the challenges of bringing a therapeutic from concept to commercialization.

Our mission is clear: Build better biotechs through seamless collaboration, informed decision-making, and accelerated progress.

For more information, please visit www.ssistrategy.com

The Higgins Group, Inc. is an executive search and consulting firm focused exclusively in the life sciences. For over two decades we’ve been helping our clients thrive by going beyond recruiting the best leaders: as a strategic partner we consult on organizational issues that affect executive integration, retention, and performance. This approach has led to long-lasting relationships with a select roster of global pharmaceutical and biotech clients, helping us to grow exclusively through referrals since 1998. Today, we offer three practices to help our life sciences clients improve performance, retain talent, and accelerate ROI: Our Executive Search Practice specializes in finding physicians and R&D executives with the credentials, qualities, and cultural fit to drive superior company performance. Our Leadership Development Practice boosts performance with executive coaching and customized workshops to integrate new executives and create sustainable leadership improvements in individuals and teams. Our Board Impact Practice enhances board decision-making by recruiting and developing diverse, high-performing leaders who can help guide life sciences firms to realize their vision. All three practices are based on a simple, powerful premise: great leaders drive great performance. To learn more, please visit www.higgins-group.com

GQR’s Life Sciences Division partners with innovative biotechs, global pharmaceutical leaders, and cutting-edge MedTech companies to deliver tailored talent solutions that align with your unique needs. We prioritize building strong partnerships that seamlessly integrate with your team and enhance your talent strategy. For more information, please visit https://www.gqr.com/disciplines/life-sciences

Since 2008, we at i-Pharm have specialized in life sciences recruitment, supporting Pharmaceutical, Biotech, MedTech and CRO companies globally. With offices in major hubs, we deliver high-quality recruitment solutions, focusing on Medical Affairs, Clinical Development, Clinical Operations, Regulatory Strategy, CMC, and Commercial sectors, driven by strong values and industry expertise. For more information, please visit https://www.i-pharmconsulting.com/

WittKieffer is the premier executive search and leadership advisory firm developing impactful leadership teams for organizations that improve quality of life. We work exclusively with organizations in life sciences, healthcare, and education. Through our executive search, interim leadership, and leadership advisory services, we strengthen organizations that make the world better. To learn more, please visit www.wittkeiffer.com

4C Pharma provides end-to-end Pharmacovigilance and Regulatory services in Medical Information Call Center, Literature Search, Case Processing, Periodic Reports, Signal and Risk Management with in-house Argus. Well versed in global regulations and systems, we provide 100% customizable safety services. We can get a quote for you in 48 hours. Info@4Cpharma.com

Alpha Clinical is a boutique consulting firm specializing in clinical development, end-to-end pharmacovigilance services, regulatory affairs, and R&D consulting. We provide comprehensive solutions, including clinical operations, site management, medical affairs, and strategic due diligence, ensuring compliance with global standards while prioritizing patient safety. Our expertise drives excellence across the pharmaceutical and biotech industries. For more information, please visit https://alphaclinicaldevelopments.com/

CRIO revolutionizes clinical research with cutting-edge cloud technology. CRIO enables remote monitoring and instant data review with CRIO Reviewer, an integrated eSource/EDC solution. Capturing data in real-time and ensuring compliance with various regulations, including 21 CFR 11, ICH-GCP, GDPR, and HIPAA, CRIO eliminates redundant data entry and safeguards data integrity. For more information, please visit https://clinicalresearch.io/

MERIT is an oncology endpoint expert providing image collection, centralized reading, and data management services for clinical trials since 2012. We have supported hundreds of trials across 58 countries. MERIT partners with CROs as well as pharma and biotech companies to deliver reliable endpoint services in global clinical trials. To learn more, please visit meritcro.com

Mesa Science Associates is a veteran-owned small business located within the Frederick Innovative Technology Center Inc. (FITCI) in Frederick, MD. Mesa provides a comprehensive array of pharmaceutical development solutions to the research community including the Federal government. From product development planning to NDA or BLA submission, Mesa’s flexible service model leverages a network of highly skilled research and research support professionals from across the United States. This allows Mesa to effectively consult with laboratory specialists concerning pharmacology, preclinical drug evaluation, clinical studies, CMC development, drug delivery system, and regulatory consulting throughout the drug approval process. To learn more, please visit www.mesascience.com.

We’re an end-to-end talent supplier - from preclinical to post market, through to research, development and technical operations. We qualify, engage and deliver candidates to your life sciences consulting jobs. Visit us to learn more about how our life science recruiters and FSP services can support your organization. For more information, please visit https://www.orbisclinical.com/

Origins is the global patient focused specialist consultancy that provides industry-leading insights and strategic counsel for our clients at critical decision points in drug development and commercialisation. To learn more, please visit www.origins-patients.com

Phastar is a leading, award-winning, specialist Biometrics CRO that provides statistical consulting, analysis, reporting, data management and data science services to small and large biotechnology, pharmaceutical and medical device companies across the world. We leverage collaboration, technology, clinical data, and our worldwide presence to optimize decision-making for safety, quality, and efficiency. With 15 offices worldwide, our number one priority is ensuring on-time, quality work and assisting our customers in optimizing their clinical research. For more information, please visit https://phastar.com/

Q2BI is a biometrical and clinical science contract research organization (CRO) for the life science industry product/drug development and regulatory submissions. Founded in 2009, Q2BI has a broad range of expertise-based services in the areas of Electronic Data Capture (EDC), Clinical Data Management (CDM), Medical Services (Medical Writing, Medical Monitoring, Medical Coding), Statistical Programming, Biostatistical science, Safety Monitoring including IDMC/DSMB, Pharmacokinetics / Pharmacodynamics (PK/PD), Data Science including data visualization/analytics and System Validation Consulting. Q2BI is a pioneer in adopting CDISC and supported the world’s first FDA Project ORBIS.

Stratacuity is a trusted boutique biotech staffing agency, founded in 2001, with a mission to drive groundbreaking scientific advancements. Our experienced scientific recruiters have a strong history of successfully placing exceptional talent at prominent life sciences companies in Boston and beyond. From assisting with critical initial hires through executive search, we are committed to supporting your success. Proven Scientific Placement

For more information, please visit https://www.stratacuity.com/

Thorough Group delivers elite biotech human capital talent solutions, connecting innovative companies with top-tier leaders and specialists. With 85+ years of expertise across our leadership team, we align mission-driven professionals to fuel breakthroughs and accelerate growth. Our strategic, insight-driven approach ensures cultural and operational fit for long-term success. For more information, please visit WWW.Thoroughgroup.com

TPS delivers customized, cost-effective solutions designed to accelerate study success. Our models drive faster study start-up, streamline site enablement, optimize patient enrollment, enhance site management, improve monitoring efficiency, and strengthen data integrity. By deploying dedicated, therapeutically aligned professionals, we ensure every aspect of your study is optimized for quality and performance. For more information, please visit https://www.tpsglobal.com/

Veristat is the scientific full-service CRO and consultancy integrating strategic planning, regulatory strategy, and clinical trial execution to rapidly advance the development, approval, and commercialization of your revolutionary therapies around the globe. The Science-First CRO™ — Veristat