Steven Cutler
Analyst · Goldman Sachs
Thank you, Brendan, and good morning to all of you. Supported by a positive outsourcing environment, encouraging levels of FDA approvals and continued strong biotech demand, 2019 resulted in another record year of ICON. Our operational focus flexible partnering approach, strong therapeutic expertise and market-leading global service offerings, all underpinned by ICON's to differentiated patient site and data strategy have enabled us to broaden our customer base with new strategic alliances across our core service lines, supplemented by continued wins from existing customers. During 2019, we were awarded our highest ever gross and net bookings of over $4.25 billion and $3.65 billion, respectively, delivering a trailing 12-month book-to-bill of 1.3x. This resulted in a year-end backlog of $8.6 billion, a year-on-year increase of 11.4%, reflecting a consistent and strong business development performance. The backlog growth helped our full year revenues increased by 8.1% year-over-year to $2.806 billion or 9.6% on a constant currency basis. Growth during 2019 outside our top 5 customers was strong at 11.4%, and we expect this to continue into 2020 as we benefit from the strong biotech funding environment and the traction we are gaining with a number of large and midsized customers. During 2019, we again demonstrated our consistent ability to drive operational efficiencies and leverage our world-class mobile business services group. We exited the year with a gross margin of 29.9% in quarter four, up from 29.4% in quarter four 2018. Our SG&A performance continues to be best-in-class our full year SG&A improving from 12.6% of revenue in 2018 to 12% of revenue in 2019. As we move forward into 2020 and beyond, we will continue to maximize our cost efficiency initiatives to drive further margin enhancement. This positive margin profile helped our EPS growth for the full year by 13% to $6.88. The core industry challenge is how to recruit and retain patients into clinical trials quickly and efficiently remains our customers' most pressing concern. This problem is prevalent in most therapeutic areas, particularly oncology, where the focus is on effectively selecting the right sizes and driving the recruitment of narrowly defined subsets of patients into trials in a timely and effective manner. ICON is committed to tackling this challenge through our patient site and data strategy. With its development being a key area of our focus in 2019 and beyond. At ICON, we understand that patients are partners, not subjects. We realize that understanding the patient's circumstance and needs and help ensure the right trial design and selection of endpoints that are relevant and meaningful. Patient input has significant value because they have different priorities and the perspectives to regulators, investigators and payers. For example, the inconvenience factor, of having monthly site visits for a patient who is in mobile must be considered when designing a trial. So the trial objectives have a good chance of being achieved. Our acquisition of Symphony clinical research, a provider of site and patient clinical trial support services, enhances our ability to conduct virtual and more hybrid trials as we move forward. With this acquisition, we are aiming to not only provide a better patient experience, but to also innovate and accelerate clinical studies. Improved in late September, this transaction offers patients at home trial services, making it more convenient and accessible for patients to participate in clinical trials. This patient-centric approach helps reduce the burden of participants, enhancing ICON's ability to recruit and retain patients. And importantly, from the patient's perspective, providing access to clinical research studies in which they may not otherwise have been able to participate. As trials become more complex and burdensome, we see significant increases in both patient eligibility criteria as well as the number of procedures required in study protocols. We are committed to reshaping and improving trial management in regards to site selection and management practices. By seeking better predictors of site and ultimately study performance. There is also a need for clinical research positions of these selected sites to be able to effectively access a variety detailed data sources to identify or for patients for their clinical trials. The opportunity to engage other physicians and colleagues to refer patients into these studies is also a key component of trial management. In quarter two, we purchased a majority shareholding in MeDiNova research and integrated site network, complementing our successful U.S. focused PMG site network, MeDiNova greatly enhanced ICON's patient recruitment and retention capabilities in Europe and South Africa by enhancing our ability to access patients. Our site network model provides an embedded clinical research offering in health care organizations with a proven method to engage physicians and patients into clinical research programs. PMG and MeDiNova offer comprehensive central trial management support in key areas of management, including study start-up, contract and budget negotiation, recruitment, retention, data collection and training. Our embedded staff also have direct access to the site's EMR database, which help you evaluate the patient population during the study feasibility phase, increasing enrollment and importantly, making clinical trial participation, a more efficient process for the position. During 2019, we were pleased to see continued evidence of our site network and health care allied sites are benefiting customs with improvements against industry benchmarks to key operational and quality metrics such as faster startup and recruitment times, fewer queries per site and less protocol deviations. In addition to the patient and site components of our strategy, we remain committed to accessing clinical research data from our innovative data partnerships as well as continuing to invest in and expand our 1 search platform. Furthermore, during 2019, ICON launched a new patient engagement platform to support improved patient experience and enrollment in clinical trials. The platform increases visibility of potential study participants to sites and sponsors and supplements patient recruitment outreach by sites. In 2019, we spent just under $147 million, repurchasing 1,035,100 shares at an average price of $141.95. During the year, we also generated strong cash collections, helping us achieve cash from operating activities of $413 million. This helped drive down our DSO to 54 days from 57 days last year. This led the company had net cash of $220.3 million compared to net cash of $106.5 million a year ago. We remain committed to deploying this cash to maximize shareholder returns through targeted strategic acquisitions. We are delighted today to continue that progress with the announcement of our fourth transaction in the past 12 months. The acquisition of MedPass international. Included in January of this year, MedPass International is a leading European medical device CRO, regulatory and reimbursement consultancy. It specializes medical device development and market access. The outsourced device market worth approximately $10 billion per annum. And while still highly fragmented is experiencing strong growth due to changing regulations, technical innovation and increasing levels of outsourcing. This acquisition further enhances and globalize ICON's current medical device and diagnostic research services group. The integration of MedPass International Services, we've noted expertise in complex class II devices, interventional cardiology and structural heart devices. The acquisition will broaden our footprint and staff headcount across Europe. Positioning us among the global leaders in this relatively new growth mark. As we look forward to quarter one and beyond, we should acknowledge the impact of the Coronavirus on our operations. The current situation remains very fluid, and we continue to take guidance from health authorities in the affected regions to ensure that ICON protects safety and well-being of our employees. And advised by government directives in various jurisdictions. Currently, monitoring visits are going ahead as scheduled, where the sites are permitting visits and many employees have been able to work from home. Our offices in China reopened this week and our laboratory in Singapore continues to function normally at this stage. However, a significant number of site monitoring visits in China have been deferred and this will have an effect on our Q1 revenues. The extent of this is unclear at present that we estimate in the range of $4 million to $7 million for quarter one. Assuming the virus is contained within the next month or so, we are optimistic that much of the deferred work can be completed in subsequent quarters 2020. Notwithstanding the challenges that the coronavirus situation brings, I want to take this opportunity to reaffirm our full year guidance. We expect 2020 to be another strong year of revenue and earnings growth, with revenue in the range of $2.972 billion to $3.092 billion, an increase of 5.9% and 0.2% and earnings per share in the range of $7.55 to $7.85, an increase of $9.7 million to 14.1%. Before moving to Q&A, I'd like to welcome all of the MedPass staff to ICON. And of course, sincerely thank the entire ICON team across the globe for all their hard work and commitment during 2019. Now ready for questions.