Thank you, David, and good afternoon, everyone. Thank you for joining Certara's second quarter earnings call. John and I will begin with prepared remarks, and then we will take your questions. Certara's second quarter performance reflects continued strength in software and made a more challenging environment in services. We have found that the pace of recovery in the market demand has been relatively mixed. There are positive signs among some biotechs, especially those in the clinical stage, but we see continued caution in the spending patterns of some Tier 1 clients. This has affected our business segments in different ways. Our software business is growing with new products, new seats and new clients as customers see the potential for our products to reduce cost and improve development outcomes. However, our services business is more dependent upon the overall progress of projects in the global development pipeline where there has been reduced spending across the industry and which has impacted our near-term commercial opportunities. That said, our conversations with customers indicate high interest in biosimulation over the long term and specifically in Certara's software and services. Second quarter total revenue grew 3% to $93.3 million which was slightly below our internal expectations. Underlying this was 13% growth in our Software segment and negative 3% growth in our Services. During the quarter, Certara made efforts to optimize the allocation of resources across the business, including cost reduction actions to better position ourselves for balance of 2024 and beyond. As we look to the future, we were encouraged to see our total bookings in the second quarter were $98.9 million, which grew 15% year-over-year. Throughout the quarter, the pace of commercial activity in our services business progressed towards the lower end of our expectations with Tier 3 customers outperforming and Tier 1 customers underperforming. We have not yet seen an inflection point at the market level in services demand, but we have seen some green shoots in the Tier 3 customer base and are encouraged by that customer group heading into the second half of the year. We believe that our Tier 1 customers have continued to evaluate spending priorities and pipeline development initiatives throughout the first half of the year. This has resulted in slower spending and elongated decision-making, impacting our services businesses. We are encouraged by 14% growth in services bookings for the second quarter. As we continued our continue strength in software, reemerging strength in biotech customers and the normal seasonality of our business, we continue to have confidence in our full year outlook, which we are reiterating today. The environment we have seen year-to-date falls within the range of outcomes we anticipated when we initiated 2024 guidance earlier this year. As we assess the remainder of the year, we believe disciplined commercial strategy, new product releases and a stable end market keeps the revenue guidance range achievable with the upper end of the guidance range possible with an improving end market outlook, but we are tracking to the lower half of revenue guidance range, given what we've seen during Q2 with our Tier 1 services customers. We will continue to focus on commercial execution as we progress through the second half of the year. Next, let's touch on some recent highlights at Certara. In the rapidly changing biopharma landscape, we're engaging with key players across the sector. During our inaugural client summit called Certainty, we brought together biosimulation experts to discuss our offerings in an interactive environment. Over 250 clients joined various tracks tailored to specific applications, networking and engaging with the Certara team. This may even include hands-on workshops for Simcyp, Phoenix and Pinnacle 21 plus a preview of the CoAuthor AI regulatory writing software. The summit proved to be an excellent platform for solidifying customer relationships and promoting model-informed drug development. We have also continued to focus on investments that support the long-term adoption of biosimulation. Last month, we announced an agreement to acquire Chemaxon, a leading provider of cheminformatics software used in the discovery phase of drug development. This acquisition is expected to close in the fourth quarter, subject to customary closing conditions. Used by 18 of the top 20 pharma companies, Chemaxon's tools span the design, make, test and analyze framework, which is used to make lead optimization and pipeline development prioritization decisions. By integrating these tools with Certara's biosimulation products and artificial intelligence technology, we can enhance the use of model-informed drug development in the discovery and lead optimization phases. Chemaxon is expected to generate 2024 software revenues of over $20 million with our team of over 200 employees, including more than 75 software developers. Their 2024 adjusted EBITDA margin is below Certara's corporate average, but we have a road map to achieve margins approaching Certara's corporate average adjusted EBITDA margin by the end of 2025. In the second quarter, we continue to make progress in developing new software products and product features and integrating AI across our portfolio. In early June, we released the 23rd version of Simcyp, which included new features such as advanced biomarker modeling to predict drug-drug interaction risks and expanded biopharmaceutics capabilities. Additionally, the new version of Simcyp aligns with recent FDA guidelines, covering pH-dependent drug-drug interactions and therapeutic proteins that should help ensure smoother regulatory processes. We also announced the highly anticipated full commercial launch of our CoAuthor regulatory writing software at DIA 2024. CoAuthor leverages generative AI to accelerate the drafting of regulatory submissions and as it demonstrated, improved efficiency to first track by greater than 30%. CoAuthor is another example of how Certara is using AI technology acquired in the Vyasa transaction to develop impactful products that can ultimately drive further market penetration. Early customer feedback has been very positive. And we expect the product will generate notable commercial interest as the year progresses. Wrapping up, we are working diligently to improve growth and profitability of the businesses in the second half year. There have been several exciting developments related to our software products this year. And we announced a strategic acquisition that will help accelerate industry adoption of model-informed drug development, particularly in the discovery phase with strong synergistic growth opportunities. We continue to attract new customers and attract and add new products features that impact drug development timelines and efficiencies. As I look forward to the rest of the year and beyond, I am confident in the investments we are making in our business and that they will translate to long-term growth. With that, I will now hand things over to John, to discuss our financial results in more detail.