2024 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 us at www.cytel.com. You also can follow us on LinkedIn and Twitter and like us on Facebook.

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.

Scimega is a niche Canadian oncology CRO acting in Canada within the context of global cutting-edge oncology trials sponsored by 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.

To learn more about the Canadian opportunity or explore an expansion with Scimega, please visit: https://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.

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/

You worry about the clinical trials—we'll help you get your asset to market. Bring your asset to life with the only cloud-based strategic planning platform that enables teams to quickly create a tailored, multi-year commercialization roadmap with a budget and hiring plan. With detailed cross-functional recommendations on what, when, and how much, the Corval® platform empowers biopharma leaders, consultants, multi-service providers, and pharmaceutical companies to navigate the commercialization process with confidence. 

Govig & Associates specializes in Executive Search for the Biotech Industry. Our emerging and midsized clients retain us repeatedly when they face timing challenges, knowledge and network gaps, resource scarcity or scope and reputation challenges. 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 www.govig.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/

Whether you are focused on improving recruitment and retention, building relationships within communities of color, or gaining actionable insights from people living with a condition of interest, Legacy is a bridge to the patients you aim to serve.

Our unique offerings and consulting approach leverages the collective intelligence of your team and ours to deliver equity-centered engagement offerings that earn trust and build partnerships with diverse communities. Together, we can advance health equity, accelerate robust drug development, and deliver more life-changing medicines to people in need. Learn more at: www.LegacyHealthStrategies.com

The Medical Affairs Consulting Team at Lumanity was developed to empower your organization to deliver impact. Our medical affairs programs are designed to help your team identify, analyze, and utilize actionable information. We can help you recognize the most critical insights from your in-house and field teams, and then capitalize on that knowledge to build your medical affairs plans, strengthen your engagement with thought leaders, and build cutting-edge data generation programs. Success in these areas allows the medical team to provide leadership and demonstrate maximum value to your brand and organization. Learn more at https://lumanity.com/solutions/strategy-consulting/medical-affairs/

Founded in 1997, Novotech is a global full-service clinical Contract Research Organization (CRO) focused on partnering with biotech companies to accelerate therapeutic development at every phase. The Company has 34 office locations worldwide, experience with over 5,000 clinical projects and has received numerous prestigious awards. Novotech’s service offerings include laboratories, Phase I facilities, drug development consulting, and regulatory expertise.

Phastar is a specialist biometrics contract research organization offering statistical consulting, clinical trial reporting, data management and data science services by providing expert consultants and managing and delivering in-house projects, FSP-style arrangements and preferred partnerships. Our number one priority is ensuring on time, quality work: every project undertaken is supervised on methodology and utilizes internal processes designed to guarantee optimal quality, inspired by 4,000 years accumulated technical experience across the company. Phastar is headquartered in London (UK) and North Carolina (US) and has 15 offices across five continents.

PPD, part of Thermo Fisher Scientific, provides clinical development and analytical services that enhance customer innovation and productivity. Utilizing patient-centered strategies and data analytics, we cover multiple therapeutic areas and include early development, all phases of clinical development, peri- and post-approval, patient recruitment, investigator sites and comprehensive laboratory services. To learn more, visit https://www.ppd.com/

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.

Putnam, an Inizio Advisory company, is a leading scientific and strategic consulting partner that helps the global life science community make confident decisions, build value, and bring life-changing innovations to clinicians and patients. For more than 30 years, our rigorous, bespoke approach and globally diverse team have delivered unrivaled depth across therapeutic areas, business functions, geographic markets, healthcare sectors, and technology platforms to maximize the human impact and commercial success of client innovations. To learn more, please visit https://www.putassoc.com/ 

Signant Health is the evidence generation company. We are focused on leveraging software, deep therapeutic and scientific knowledge, and operational expertise to consistently capture, aggregate, and reveal quality evidence for clinical studies across traditional, virtual, and hybrid trial models. To learn more, please visit www.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.

SSI Strategy is a boutique consultancy that provides innovative options for building and resourcing R&D functions in growing biotech organizations. Our team of fractional R&D leadership and trained management consultants provide a unique support structure for growing organizations to derisk building, scaling, or transforming critical functions. While most organizations struggle to resource the right skills at the right time for growth in a capital scarce environment, SSI has demonstrated that there are alternative options to the organic hiring strategy.

Tasso is an emerging healthcare technology company that is transforming the traditional blood collection paradigm with a patient-centric approach. The company’s devices enable simple, convenient, and virtually painless blood collection for users. Tasso technology has the power to bring healthcare anywhere, any time. Headquartered in Seattle, Washington, Tasso is privately held and funded by grants, investments, and co-development deals with various industry leaders. For more information, please visit www.tassoinc.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

Founded in 2000, BioSearch Recruiting is a retained executive search firm focused on placing leaders of R&D, Clinical Development, Medical Affairs, Regulatory Affairs and CMC. We specialize in CMO searches and building clinical organizations, including physicians at all levels and leaders across key functions. From nimble start-ups to established global enterprises, we partner closely with our clients to attract top talent, identify cultural fit and create high impact teams. Please visit us at: https://www.biosearchrecruiting.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/

Miras Search Partners is a boutique pharmaceutical and biotechnology specialty Executive Search and Recruitment Firm. Our well-established M.D. Practice helps early/later development, and commercial stage companies hire M.D.s at all levels for CMO, Therapeutic Area Heads, Global Program Leaders, Clinical Development Leads, and Global/US Medical Affairs roles. Visit: https://mirassp.com/md-specialty-practice/

Sano’s end-to-end precision medicine platform combines patient finding, genetic testing, and long-term engagement all in one place. Proven to accelerate enrollment, simplify operations, and de-risk trials, it enables clinical operations teams to move 10x faster and reduce costs by 5x.

ZS is a management consulting and technology firm focused on transforming global healthcare and beyond. We leverage our leading-edge analytics, plus the power of data, science and products, to help our clients make more intelligent decisions, deliver innovative solutions and improve outcomes for all. Founded in 1983, ZS has more than 12,000 employees in 35 offices worldwide. To learn more, visit https://www.zs.com/or follow us on Twitter and LinkedIn.

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/.

Established in 2009, Green Key Pharma works with pharmaceutical, biotech, medical device and CRO's nationwide. Our mission is to forge powerful connections among ourselves, our candidates, and the clients we serve. We are committed to empowering everyone with whom we collaborate to construct a brighter future. Learn more at https://www.greenkeyllc.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.

Phesi's patient-centric data analytics solutions deliver smarter trials and faster cures. We use our AI-driven Trial Accelerator™ platform with global data from 100 million patients, 195 countries and 4,000 indications to create Digital Patient Profiles and our unique Patient Access Score to assess investigator potential. We deliver actionable insights with unrivalled precision to enable you to optimize protocol design, improve enrollment and reduce patient burden and cycle times. Trial Accelerator has been proven to deliver innovative medicines including Keytruda. We can also help you revolutionize clinical development with Digital Twins and Digital Trial Arms. Learn more at phesi.com

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 over 20 years, Valos Srl has been seen as a foremost organization in the field of biostatistics and data managment services for Phase I-IV Clinical Trials. With professional experience in drug and device development studies, VALOS offers operational excellence and tailored services while providing high quality research to bolster clients' resounding successes. With a powerhouse team in place, in-depth knowledge of the pharmaceutical and biotech industries and intensive experience, VALOS aims to support its pharma clients set new benchmarks in clinical trials and scale newer heights.

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