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Courage
Showing empathy for those impacted by challenging diseases, daring to innovate, leading the field, taking ownership and risks, being vulnerable and humble, and learning from failure.
Pentara has shepherded 100+ regulatory submissions toward approval, primarily in neurodegenerative disease. We pair methodological rigor with operational clarity so that what your data actually shows is what reaches the reviewer.
Pentara was founded in 2001 and has been led by Dr. Suzanne Hendrix, PhD, since 2008. We have become internationally recognized for deep expertise across therapeutic areas and for services spanning every phase of clinical trial design, implementation, evaluation, regulatory submission, and publication.
Notably, Pentara invests its own resources to advance research in Alzheimer's and other neurodegenerative diseases. Without government or pharmaceutical industry funding, we maintain unbiased expertise and accelerate effective treatments wherever they emerge.
Statistics
Informatics
Data Management
Biostatistics
Medical Writing
2001
Founded in Utah
200+
Publications
01
Showing empathy for those impacted by challenging diseases, daring to innovate, leading the field, taking ownership and risks, being vulnerable and humble, and learning from failure.
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Working together as one organization to help each other succeed, embracing the value of diverse perspectives, partnering and aligning with our clients to achieve shared goals.
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Operating with honesty and transparency, ensuring the highest ethical standards.
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Consistently providing high quality data and services through automation, standardization, efficiency, and continued process improvement.
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Relentlessly pursuing solutions, performing at our best to improve lives, always motivated by patient and client needs.
"We make a disproportionately large splash in the field compared to our size. We really change the world."
Kent Hendrix, Co-Founder
Decades of trial experience across academia, CROs, and large and small pharma. Expand any profile to read the full biography.
Suzanne Hendrix graduated from Boston University with a Ph.D. in mathematics. Dr. Hendrix has worked as a clinical trials statistician, and has now accumulated over 30 years of experience with time spent at CROs and pharmaceutical companies, including projects across many disease areas. Since becoming CEO of Pentara in 2008, Dr. Hendrix has maintained a central focus on analysis of clinical trials for degenerative diseases, especially Alzheimer’s disease (AD). Suzanne has first authored or co-authored over 150 peer-reviewed publications related to both clinical trial results and statistical approaches for clinical trials, many of which include significant contributions to statistical methodology for Alzheimer’s disease. Dr. Hendrix also played an important role in the development of ADCOMS, an AD composite score to measure cognitive function in individuals with mild cognitive impairment due to AD. Overall, Suzanne’s main goal for Pentara is to “give studies and clients the best chance of success for effective treatments” by implementing better standards and methods for statistical analysis and study design that guarantee accurate results with clinical data. When asked about what she loves most about her company, Dr. Hendrix emphatically responded, “the people! We have the smartest, nicest people, and I like that we’ve found so many creative thinkers.” In her free time, Suzanne participates in Crossfit, and especially enjoys working out with her kids.
Kent Hendrix, BSSr. Vice President of Informatics
Kent Hendrix has 33 years experience in the Pharmaceutical industry, including all aspects of statistical programming in SAS, and has handled a broad variety of clinical trials and data analysis projects. He has worked on many NDAs and managed multiple groups of SAS programmers. Mr. Hendrix has taught SAS programming at Brigham Young University and AP Statistics and Computer Science at the high school level. Mr. Hendrix also developed a SAS program Log File Analysis tool that helps SAS programmers debug their code faster. Additionally, Kent developed a web-based clinical trial management software that handles the enrollment and randomization of subjects, drug distribution to sites, and allocation to subjects. This software has managed global phases I, II, and III clinical trials. As one of the founders of Pentara, Kent has loved watching the company grow. He loves that Pentara makes a “disproportionately large splash in the field compared to our size. We really change the world.” When he isn’t working, Mr. Hendrix can be found teaching Bushikai Kishindo Martial Arts , in which he holds a 10th degree black belt. He also enjoys reading and fishing in the beautiful Utah mountains.
Samuel Dickson, PhDSr. Vice President of Statistics
Sam Dickson has a Ph.D. in statistics and bioinformatics and has been working in clinical trials since 2003. As Vice President of Statistics at Pentara Corporation, he consults with clients on study design and analysis of neurodegenerative diseases, including Alzheimer's disease, Parkinson's disease, and ALS. One area of particular interest to Dr. Dickson is finding or developing appropriate and meaningful outcomes to be able to detect treatment effects in progressive diseases, which are generally heterogeneous and difficult to measure with precision. He is an expert in clinical trial design for phase 2 and phase 3 clinical trials, including group sequential designs, sample size re-estimation, and Bayesian adaptive studies. His background includes experience working with research and clinical data at GlaxoSmithKline, Duke University, the United States Army, Pfizer, and a public health company. Dr. Dickson has worked on treatments for a wide range of conditions including the Ebola virus, malaria, dengue, macular degeneration, pain, schizophrenia, laser hair removal, and other cosmetic devices. He also has experience with whole genome and exome sequencing data and helped to develop a polygenic risk score for Alzheimer's disease. Dr. Dickson believes everyone was born Bayesian.
Jessie Nicodemus-Johnson, PhDSr. Vice President of Biostatistics
Jessie Nicodemus Johnson is the Senior Vice President of Biostatistics at Pentara Corporation. She joined Pentara Corporation in 2020, bringing over 15 years of experience in statistics, study design, and integrative physiology. Jessie and her team manage a diverse array of client needs including clinical trial design, CDISC dataset generation, Ad Hoc analyses supportive of study design, and post hoc analyses of study outcomes. Jessie specializes in incorporating the clinical and underlying molecular aspects of treatment efficacy with statistical methodology resulting in a more thorough understanding of associations with outcomes of interest. Jessie received her PhD in Molecular and Integrative Physiology from the University of Illinois: Urbana-Champaign in 2010 and continued to cultivate her understanding and love of systems biology and statistics during her postdoc at the University of Chicago in the Department of Human Genetics. When not working, Jessie enjoys spending time with her kids in the mountains surrounding Salt Lake City.
Craig Mallinckrodt, PhDDistinguished Biostatistician
Craig is a Distinguished Biostatistician at Pentara where he contributes broadly to support client’s research in Alzheimer’s and other diseases. Craig joined Pentara in 2022 after 30 years of clinical trial experience in academia and at large and small pharma companies. He is a Fellow of the American Statistical Association and won the Royal Statistical Society’s award for Outstanding Contribution to the Pharmaceutical Industry. Dr. Mallinckrodt led the statistical work that resulted in global regulatory approvals for drugs in 10 indications. Craig also led industry working groups on methodology topics, including placebo response, missing data, and estimands and sensitivity analyses. He has authored four books and 200 manuscripts on various statistical and clinical topics. Dr. Mallinckrodt led much of the early research into the MMRM analytic approach that resulted in this method’s widespread use in longitudinal clinical trials. A native of Missouri and long-time resident of Colorado, where he got his BS, MS, and PhD (1993) at Colorado State University, Craig now resides with his wife Donna in Indianapolis, IN. Donna is a licensed Medicare Insurance Specialist with a passion for helping the elderly. Their daughter, Marissa, is a nurse in Chicago where she continues Donna’s passion for helping others. Craig enjoys running, having logged over 100,000 miles lifetime, and winning a bronze medal at the 1996 Paralympics. He also enjoys cycling, skiing and wildlife photography.
Christina Lewis, MSDirector of Clinical Programming
Christina Lewis is the Director of Clinical Programming at Pentara. She leads a team of programmers that creates submission-ready SDTM packages and provides programming support for data review and cleaning. Christina earned a Master's degree in Statistics from the University of Utah which ensures each of her projects have the end analyses in mind even if the specific work being done does not involve statistics. She has provided SDTM dataset for multiple FDA submissions. During her time in this industry, Christina has learned the importance of applying CDISC standards as early in the process as possible such that the protocol and EDC build lead to smooth transition from raw to SDTM data. She is passionate about findings new ways to automate tedious tasks to ensure the accuracy and efficiency of her team.
Newman Knowlton, MSVP of Corporate Development
VP of Corporate Development Newman Knowlton received his Master’s degree in Quantitative Psychology from McGill University in Montreal, Quebec in 2017. Mr. Knowlton started working at Pentara in January of 2018 as Pentara’s fifth employee. While at Pentara, he has presented at several conferences, contributed to several papers, and was the lead on an NDA for an ALS drug (AMX0035). Since he was one of the first to join the Pentara team, Newman’s favorite thing about the company is seeing it grow. He takes pride in Pentara’s work and is happy to see the team getting bigger and receiving more recognition. Outside of the office, Newman enjoys yoga, and civil engineering, as well as playing tennis and renovating houses. Among all of his hobbies and talents, Newman is the most proud of his 1996 Honda Civic.
Jeffery Yearley, BASr. Director of Quality
Jeffery Yearley is a strategic leader with over 20 years of experience in data management, governance, and quality assurance. His expertise is focused on designing and implementing enterprise-wide Quality Management Systems (QMS) and data governance frameworks that ensure regulatory compliance (GCP, 21 CFR Part 11, GDPR, ISO 27001). He has a proven track record of modernizing data platforms to enable innovation and growth, building high-performing teams, and fostering a culture of data quality and excellence. His work has significantly enhanced data governance maturity, security, and accessibility across clinical research and life sciences organizations.
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